UCSF Pharmacogenetics of Membrane Transporters
Transporter List

Field Selection Option


HGNC SymbolHGNC DescriptionCommon NameOMIMOMIM PhenotypeNucleotide RefSeqProtein RefSeqEntrezIsoformsExperiments
ABCA1ATP-binding cassette, sub-family A (ABC1), member 1ABC1600046Tangier disease; High density lipoprotein deficiency, type 2; Tangier disease, variant; High density lipoprotein deficiency; Coronary heart disease in familial hypercholesterolema, protection aganistNM_005502NP_0054931996
ABCA2ATP-binding cassette, sub-family A (ABC1), member 2ABC2600047 NM_001606NP_0015972022
ABCA3ATP-binding cassette, sub-family A (ABC1), member 3ABC3601615Surfactant deficiency, neonatalNM_001089NP_0010802131
ABCA4ATP-binding cassette, sub-family A (ABC1), member 4ABC10601691Startgardt disease 1; Macular degeneratons, age-related, 2; Retinitis pigmentosa 19; Cone-rod dystrophy 3; Fundus flavimaculatusNM_000350NP_0003412411
ABCA5ATP-binding cassette, sub-family A (ABC1), member 5ABC13612503 NM_172232NP_7584242346142
ABCA6ATP-binding cassette, sub-family A (ABC1), member 6ABCA6612504 NM_080284NP_5250232346011
ABCA7ATP-binding cassette, sub-family A (ABC1), member 7ABCX605414 NM_019112NP_0619851034711
ABCA8ATP-binding cassette, sub-family A (ABC1), member 8ABCA8612505 NM_007168NP_0090991035153
ABCA9ATP-binding cassette, sub-family A (ABC1), member 9ABCA9612507 NM_080283NP_5250221035051
ABCA10ATP-binding cassette, sub-family A (ABC1), member 10ABCA10612508 NM_080282NP_5250211034921
ABCA12ATP-binding cassette, sub-family A (ABC1), member 12LI2607800Ichthyosis, lamellar 2NM_173076NP_7750992615421
ABCA13ATP-binding cassette, sub-family A (ABC1), member 13ABCA13607807 NM_152701NP_68991415466441
ABCB1ATP-binding cassette, sub-family B (MDR/TAP), member 1MDR1171050Colchicine resistance, Crohn diseaseNM_000927NP_0009185243142
ABCB4ATP-binding cassette, sub-family B (MDR/TAP), member 4MDR3171060Cholestasis, familial intrahepatic, of pregnancy; Cholestasis, progressive familial intrahepatic, type III; CholelithiasisNM_000443NP_0004345244328
ABCB5ATP-binding cassette, sub-family B (MDR/TAP), member 5ABCB5611785 NM_178559NP_84865434027351
ABCB6ATP-binding cassette, sub-family B (MDR/TAP), member 6ABC14605452 NM_005689NP_0056801005831
ABCB7ATP-binding cassette, sub-family B (MDR/TAP), member 7ABC7300135Anemia, sideroblastic, and spinocerebellar ataxiaNM_004299NP_0042902251
ABCB8ATP-binding cassette, sub-family B (MDR/TAP), member 8MABC1605464 NM_007188NP_0091191119471
ABCB9ATP-binding cassette, sub-family B (MDR/TAP), member 9TAPL605453 NM_019625NP_0625712345771
ABCB10ATP-binding cassette, sub-family B (MDR/TAP), member 10M-ABC2605454 NM_012089NP_0362212345611
ABCB11ATP-binding cassette, sub-family B (MDR/TAP), member 11BSEP603201Progressive intrahepatic cholestasis-2NM_003742NP_0037338647228
ABCC1ATP-binding cassette, sub-family C (CFTR/MRP), member 1MRP1158343 NM_004996NP_0049874363534
ABCC2ATP-binding cassette, sub-family C (CFTR/MRP), member 2MRP2601107Dubin-Johnson syndromeNM_000392NP_0003831244231
ABCC3ATP-binding cassette, sub-family C (CFTR/MRP), member 3MRP3604323 NM_003786NP_0037778714333
ABCC4ATP-binding cassette, sub-family C (CFTR/MRP), member 4MRP4605250 NM_005845NP_00583610257633
ABCC5ATP-binding cassette, sub-family C (CFTR/MRP), member 5MRP5605251 NM_005688NP_00567910057729
ABCC6ATP-binding cassette, sub-family C (CFTR/MRP), member 6MRP6603234Pseudoxanthoma elasticum, autosomal dominant; Pseudoxanthoma elasticum, autosomal recessive; Pseudoxanthoma elasticum, sporadicNM_001171NP_001162368423
ABCC8ATP-binding cassette, sub-family C (CFTR/MRP), member 8SUR1600509Persistent Hyperinsulinemic Hypoglycemia of Infancy; Persistent Hyperinsnulinemic Hypoglycemia of Infancy due to Focal Adenomatous HyperplasiaNM_000352NP_000343683322
ABCC9ATP-binding cassette, sub-family C (CFTR/MRP), member 9SUR2601439cardiomyopathy, dilated with ventricular tachycardiaNM_005691NP_00568210060102
ABCC10ATP-binding cassette, sub-family C (CFTR/MRP), member 10ABCC10612509 NM_033450NP_2582618984585
ABCC11ATP-binding cassette, sub-family C (CFTR/MRP), member 11ABCC11607040 NM_032583NP_1159728532062
ABCC12ATP-binding cassette, sub-family C (CFTR/MRP), member 12MRP9607041 NM_033226NP_1502299416011
ABCC13ATP-binding cassette, sub-family C (CFTR/MRP), member 13, pseudogenePRED6608835   15000001
ABCD1ATP-binding cassette, sub-family D (ALD), member 1ALD300371Adrenoleukodystrophy; Addison disease; AdrenomyeloneuropathyNM_000033NP_00002421511
ABCD2ATP-binding cassette, sub-family D (ALD), member 2ABC39601081 NM_005164NP_00515522518
ABCD3ATP-binding cassette, sub-family D (ALD), member 3ABC43170995Zellweger syndrome 2NM_002858NP_002849582561
ABCD4ATP-binding cassette, sub-family D (ALD), member 4ABC41603214 NM_005050NP_0050415826211
ABCE1ATP-binding cassette, sub-family E (OABP), member 1ABC38601213 NM_001040876NP_001035809605921
ABCF1ATP-binding cassette, sub-family F (GCN20), member 1ABC27,ABC50603429 NM_001025091NP_0010202622390
ABCF2ATP-binding cassette, sub-family F (GCN20), member 2ABC28612510 NM_005692NP_0056831006131
ABCF3ATP-binding cassette, sub-family F (GCN20), member 3ABCF3  NM_018358NP_0608285532431
ABCG1ATP-binding cassette, sub-family G (WHITE), member 1ABC8603076 NM_004915NP_004906961974
ABCG2ATP-binding cassette, sub-family G (WHITE), member 2MXR603756 NM_004827NP_0048189429520
ABCG4ATP-binding cassette, sub-family G (WHITE), member 4WHITE2607784 NM_022169NP_0714526413721
ABCG5ATP-binding cassette, sub-family G (WHITE), member 5ABCG5605459SitosterolemiaNM_022436NP_0718816424043
ABCG8ATP-binding cassette, sub-family G (WHITE), member 8ABCG8605460SitosterolemiaNM_022437NP_0718826424122
AQP4aquaporin 4 600308 NM_001650NP_001641361312
ATP7AATPase, Cu++ transporting, alpha polypeptideATP7A300011Menkes disease, mild; Occipital horn syndrome; Cutis laxa, neonatal; Menkes disease; Menkes disease, copper-replacement responsiveNM_000052NP_00004353890
ATP7BATPase, Cu++ transporting, beta polypeptideATP7B606882Wilson diseaseNM_000053NP_000044540150
ATP8B1ATPase, aminophospholipid transporter, class I, type 8B, member 1FIC1602397Cholestasis, benign recurrent intrahepatic; Cholestasis, progressive familial intrahepatic-1; Byler diseaseNM_005603NP_0055945205124
CFTRcystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)CFTR602421cystic fibrosisNM_000492NP_000483108014
HTR2A5-hydroxytryptamine (serotonin) receptor 2A, G protein-coupled 182135 NM_000621NP_000612335620
HTR2C5-hydroxytryptamine (serotonin) receptor 2C, G protein-coupled 312861 NM_000868NP_000859335830
HTR3B5-hydroxytryptamine (serotonin) receptor 3B, ionotropic 604654 NM_006028NP_006019917710
MAOAmonoamine oxidase A 309850 NM_000240NP_000231412820
NR1I2nuclear receptor subfamily 1, group I, member 2PXR603065 NM_003889NP_003880885640
PORP450 (cytochrome) oxidoreductase 124015 NM_000941NP_0009325447712
RHAGRh-associated glycoprotein 180297 NM_000324NP_000315600510
RHBGRh family, B glycoprotein (gene/pseudogene) 607079 NM_020407NP_0651405712730
RHCGRh family, C glycoprotein 605381 NM_016321NP_0574055145810
SLC1A1solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1EAAC1133550 NM_004170NP_004161650510
SLC1A2solute carrier family 1 (glial high affinity glutamate transporter), member 2EAAT2600300Amyotryphic lateral sclerosisNM_004171NP_004162650650
SLC1A3solute carrier family 1 (glial high affinity glutamate transporter), member 3EAAT1600111 NM_004172NP_004163650740
SLC1A4solute carrier family 1 (glutamate/neutral amino acid transporter), member 4SATT600229 NM_003038NP_003029650920
SLC1A5solute carrier family 1 (neutral amino acid transporter), member 5ASCT2109190 NM_005628NP_005619651040
SLC1A6solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6EAAT4600637 NM_005071NP_005062651130
SLC1A7solute carrier family 1 (glutamate transporter), member 7AAAT604471 NM_006671NP_006662651230
SLC2A1solute carrier family 2 (facilitated glucose transporter), member 1GLUT138140Glucose transport defect, blood-brain barrierNM_006516NP_006507651320
SLC2A2solute carrier family 2 (facilitated glucose transporter), member 2GLUT2138160Diabetes mellitus, noninsulin-dependent; Fanconi-bickel syndromeNM_000340NP_000331651430
SLC2A3solute carrier family 2 (facilitated glucose transporter), member 3GLUT3138170 NM_006931NP_008862651530
SLC2A3P1solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 1     10012806200
SLC2A4solute carrier family 2 (facilitated glucose transporter), member 4GLUT4138190Diabetes mellitus, noninsulin-dependentNM_001042NP_001033651710
SLC2A4RGSLC2A4 regulator 609493 NM_020062NP_0644465673110
SLC2A5solute carrier family 2 (facilitated glucose/fructose transporter), member 5GLUT5138230 NM_003039NP_003030651840
SLC2A6solute carrier family 2 (facilitated glucose transporter), member 6GLUT6606813 NM_017585NP_0600551118240
SLC2A7solute carrier family 2 (facilitated glucose transporter), member 7GLUT7610371 NM_207420NP_99730315518410
SLC2A8solute carrier family 2 (facilitated glucose transporter), member 8GLUT8605245 NM_014580NP_0553952998840
SLC2A9solute carrier family 2 (facilitated glucose transporter), member 9GLUT9606142 NM_001001290NP_0010012905660630
SLC2A10solute carrier family 2 (facilitated glucose transporter), member 10GLUT10606145 NM_030777NP_1104048103110
SLC2A11solute carrier family 2 (facilitated glucose transporter), member 11GLUT11610367 NM_001024938NP_0010201096603530
SLC2A12solute carrier family 2 (facilitated glucose transporter), member 12GLUT12610372 NM_145176NP_66015915409110
SLC2A13solute carrier family 2 (facilitated glucose transporter), member 13HMIT611036 NM_052885NP_44311711413430
SLC2A14solute carrier family 2 (facilitated glucose transporter), member 14GLUT14611039 NM_153449NP_70315014419580
SLC3A1solute carrier family 3 (amino acid transporter heavy chain), member 1ATR1104614CystinuriaNM_000341NP_000332651910
SLC3A2solute carrier family 3 (amino acid transporter heavy chain), member 24F2158070 NM_001012661NP_001012679652041
SLC4A1solute carrier family 4 (anion exchanger), member 1CD233109270Band 3 memphis; Ovalocytosis, southeast asian; Spherocytosis, hereditarty, due to band 3 tuscaloosa; Hemolytic anemia due to band 3 montefiore; Spherocytosis, hereditary, due to band 3 pargue; Spherocytosis, hereditary, due to band 3 chur; Spherocytosis,NM_000342NP_000333652130
SLC4A1APsolute carrier family 4 (anion exchanger), member 1, adaptor protein 602655 NM_018158NP_0606282295010
SLC4A2solute carrier family 4 (anion exchanger), member 2AE2109280 NM_003040NP_003031652260
SLC4A3solute carrier family 4 (anion exchanger), member 3AE3106195 NM_005070NP_00506650850
SLC4A4solute carrier family 4 (sodium bicarbonate cotransporter), member 4KNBC603345Renal tubular acidosis, proximal, with ocular abnormalitiesNM_001098484NP_001091954867160
SLC4A5solute carrier family 4 (sodium bicarbonate cotransporter), member 5NBC4606757 NM_021196NP_0670195783560
SLC4A7solute carrier family 4, sodium bicarbonate cotransporter, member 7 603353 NM_003615NP_0036069497150
SLC4A8solute carrier family 4, sodium bicarbonate cotransporter, member 8NBC3605024 NM_001039960NP_001035049949850
SLC4A9solute carrier family 4, sodium bicarbonate cotransporter, member 9AE4610207 NM_031467NP_1136558369770
SLC4A10solute carrier family 4, sodium bicarbonate transporter, member 10SLC4A10605556 NM_022058NP_0713415728270
SLC4A11solute carrier family 4, sodium borate transporter, member 11BTR1610206 NM_032034NP_1144238395960
SLC5A1solute carrier family 5 (sodium/glucose cotransporter), member 1SGLT1182380Glucose/galactose malabsorptionNM_000343NP_0003346523215
SLC5A2solute carrier family 5 (sodium/glucose cotransporter), member 2SGLT2182381Renal glucosuriaNM_003041NP_003032652410
SLC5A3solute carrier family 5 (sodium/myo-inositol cotransporter), member 3SMIT600444 NM_006933NP_008864652640
SLC5A4solute carrier family 5 (glucose activated ion channel), member 4SGLT3  NM_014227NP_055042652710
SLC5A5solute carrier family 5 (sodium/iodide cotransporter), member 5NIS601843Thyroid hormonogenesis, genetic defect in, INM_000453NP_000444652820
SLC5A6solute carrier family 5 (sodium/multivitamin and iodide cotransporter), member 6SMVT604024 NM_021095NP_066918888410
SLC5A7solute carrier family 5 (sodium/choline cotransporter), member 7CHT1608761 NM_021815NP_0685876048230
SLC5A8solute carrier family 5 (sodium/monocarboxylate cotransporter), member 8AIT608044 NM_145913NP_66601816072810
SLC5A9solute carrier family 5 (sodium/sugar cotransporter), member 9SGLT4  NM_001011547NP_00101154720001050
SLC5A10solute carrier family 5 (sodium/sugar cotransporter), member 10SGLT5  NM_001042450NP_00103591512520650
SLC5A11solute carrier family 5 (sodium/inositol cotransporter), member 11SGLT6610238 NM_052944NP_44317611558490
SLC5A12solute carrier family 5 (sodium/monocarboxylate cotransporter), member 12SLC5A12612455 NM_178498NP_84859315996310
SLC6A1solute carrier family 6 (neurotransmitter transporter), member 1GAT1137165 NM_003042NP_0030336529313
SLC6A2solute carrier family 6 (neurotransmitter transporter), member 2NET163970Orthostatic intoleranceNM_001043NP_0010346530415
SLC6A3solute carrier family 6 (neurotransmitter transporter), member 3DAT126455 NM_001044NP_0010356531115
SLC6A4solute carrier family 6 (neurotransmitter transporter), member 4SERT182138Long/short promoter polymorphism; Obsessive-compulsive disorder, susceptibility toNM_001045NP_001036653221
SLC6A5solute carrier family 6 (neurotransmitter transporter), member 5GLYT2604159 NM_004211NP_004202915221
SLC6A6solute carrier family 6 (neurotransmitter transporter), member 6TAUT186854 NM_001134367NP_001127839653330
SLC6A7solute carrier family 6 (neurotransmitter transporter), member 7PROT606205 NM_014228NP_055043653411
SLC6A8solute carrier family 6 (neurotransmitter transporter), member 8CT1300036Creatine deficiency syndrome, X-linked; Mental retardation, X-linked, with seizures, short stature, and midface hypoplasia; Mental retardation, X-linkedNM_005629NP_005620653550
SLC6A9solute carrier family 6 (neurotransmitter transporter, glycine), member 9GLYT1601019 NM_201649NP_964012653661
SLC6A11solute carrier family 6 (neurotransmitter transporter), member 11GAT3607952 NM_014229NP_055044653810
SLC6A12solute carrier family 6 (neurotransmitter transporter), member 12BGT1603080 NM_003044NP_003035653991
SLC6A13solute carrier family 6 (neurotransmitter transporter), member 13 615097 NM_016615NP_057699654080
SLC6A14solute carrier family 6 (amino acid transporter), member 14SLC6A14300444 NM_007231NP_0091621125411
SLC6A15solute carrier family 6 (neutral amino acid transporter), member 15V7-3607971 NM_018057NP_0605275511731
SLC6A16solute carrier family 6, member 16NTT5607972 NM_014037NP_0547562896831
SLC6A17solute carrier family 6 (neutral amino acid transporter), member 17SLC6A17610299 NM_001010898NP_00101089838866211
SLC6A18solute carrier family 6 (neutral amino acid transporter), member 18Xtrp2610300 NM_182632NP_87243834893221
SLC6A19solute carrier family 6 (neutral amino acid transporter), member 19HND608893Hartnup disorderNM_001003841NP_00100384134002421
SLC6A20solute carrier family 6 (proline IMINO transporter), member 20Xtrp3605616 NM_020208NP_0645935471631
SLC7A1solute carrier family 7 (cationic amino acid transporter, y+ system), member 1CAT1104615 NM_003045NP_003036654120
SLC7A2solute carrier family 7 (cationic amino acid transporter, y+ system), member 2CAT2601872 NM_001008539NP_001008539654270
SLC7A3solute carrier family 7 (cationic amino acid transporter, y+ system), member 3ATRC3,CAT3300443 NM_001048164NP_0010416298488920
SLC7A4solute carrier family 7, member 4CAT4603752 NM_004173NP_004164654530
SLC7A5solute carrier family 7 (amino acid transporter light chain, L system), member 5LAT1-5600182 NM_003486NP_0034778140113
SLC7A6solute carrier family 7 (amino acid transporter light chain, y+L system), member 6SLC7A6605641 NM_001076785NP_001070253905750
SLC7A6OSsolute carrier family 7, member 6 opposite strand   NM_032178NP_1155548413820
SLC7A7solute carrier family 7 (amino acid transporter light chain, y+L system), member 7LAT1-7603593Lysinuric protein intoleranceNM_001126105NP_001119577905629
SLC7A8solute carrier family 7 (amino acid transporter light chain, L system), member 8SLC7A8604235 NM_012244NP_0363762342840
SLC7A9solute carrier family 7 (amino acid transporter light chain, bo,+ system), member 9SLC7A9604144Cystinuria, type II; Cystinuria, type III; Cystinuria, type II or IIINM_001126335NP_0011198071113640
SLC7A10solute carrier family 7 (neutral amino acid transporter light chain, asc system), member 10SLC7A10607959 NM_019849NP_0628235630110
SLC7A11solute carrier family 7 (anionic amino acid transporter light chain, xc- system), member 11SLC7A11607933 NM_014331NP_0551462365721
SLC7A13solute carrier family 7 (anionic amino acid transporter), member 13AGT1  NM_138817NP_62017215772420
SLC7A14solute carrier family 7, member 14   NM_020949NP_0660005770910
SLC8A1solute carrier family 8 (sodium/calcium exchanger), member 1NCX1182305 NM_001112800NP_001106271654680
SLC8A2solute carrier family 8 (sodium/calcium exchanger), member 2NCX2601901 NM_015063NP_055878654320
SLC8A3solute carrier family 8 (sodium/calcium exchanger), member 3NCX3607991 NM_033262NP_150287654780
SLC8B1solute carrier family 8 (sodium/lithium/calcium exchanger), member B1 609841 XM_005253939XP_0052539968002430
SLC9A1solute carrier family 9, subfamily A (NHE1, cation proton antiporter 1), member 1NHE1107310 NM_003047NP_003038654810
SLC9A2solute carrier family 9, subfamily A (NHE2, cation proton antiporter 2), member 2NHE2600530 NM_003048NP_003039654910
SLC9A3solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3NHE3182307 NM_004174NP_004165655021
SLC9A3P1solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 pseudogene 1     655100
SLC9A3R1solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 1 604990 NM_004252NP_004243936810
SLC9A3R2solute carrier family 9, subfamily A (NHE3, cation proton antiporter 3), member 3 regulator 2 606553 NM_001130012NP_001123484935170
SLC9A4solute carrier family 9, subfamily A (NHE4, cation proton antiporter 4), member 4NHE4600531 NM_001011552NP_00101155238901520
SLC9A5solute carrier family 9, subfamily A (NHE5, cation proton antiporter 5), member 5NHE5600477 NM_004594NP_004585655310
SLC9A6solute carrier family 9, subfamily A (NHE6, cation proton antiporter 6), member 6NHE6300231 NM_001042537NP_0010360021047950
SLC9A7solute carrier family 9, subfamily A (NHE7, cation proton antiporter 7), member 7NHE7300368 NM_032591NP_1159808467970
SLC9A8solute carrier family 9, subfamily A (NHE8, cation proton antiporter 8), member 8NHE8612730 NM_015266NP_0560812331520
SLC9A9solute carrier family 9, subfamily A (NHE9, cation proton antiporter 9), member 9NHE9608396 NM_173653NP_77592428519520
SLC9C1solute carrier family 9, subfamily C (Na+-transporting carboxylic acid decarboxylase), member 1SLC9A10612738 NM_183061NP_89888428533520
SLC9C2solute carrier family 9, member C2 (putative)SLC9A11  NM_178527NP_84862228452510
SLC10A1solute carrier family 10 (sodium/bile acid cotransporter), member 1SBAT1,NTCP182396 NM_003049NP_003040655411
SLC10A2solute carrier family 10 (sodium/bile acid cotransporter), member 2SBAT2601295Bile acid malabsorption, primaryNM_000452NP_000443655510
SLC10A3solute carrier family 10, member 3P3312090 NM_019848NP_062822827390
SLC10A4solute carrier family 10, member 4SLC10A4  NM_152679NP_68989220178010
SLC10A5solute carrier family 10, member 5P5  NM_001010893NP_00101089334705110
SLC10A6solute carrier family 10 (sodium/bile acid cotransporter), member 6 613366 NM_197965NP_93206934527420
SLC10A7solute carrier family 10, member 7 611459 NM_032128NP_1155048406850
SLC11A1solute carrier family 11 (proton-coupled divalent metal ion transporter), member 1NRAMP1600266 NM_000578NP_0005696556411
SLC11A2solute carrier family 11 (proton-coupled divalent metal ion transporter), member 2DMT1600523 NM_000617NP_00060848911417
SLC12A1solute carrier family 12 (sodium/potassium/chloride transporter), member 1SLC12A1600839Bartter syndrome, antenatal, type 1NM_000338NP_000329655740
SLC12A2solute carrier family 12 (sodium/potassium/chloride transporter), member 2BSC600840 NM_001046NP_001037655820
SLC12A3solute carrier family 12 (sodium/chloride transporter), member 3TSC600968Gitelman syndromeNM_000339NP_000330655941
SLC12A4solute carrier family 12 (potassium/chloride transporter), member 4KCC1604119 NM_005072NP_005063656050
SLC12A5solute carrier family 12 (potassium/chloride transporter), member 5KCC2606726 NM_001134771NP_0011282435746830
SLC12A6solute carrier family 12 (potassium/chloride transporter), member 6KCC3604878Agenesis of the corpus callosum with peripheral neuropathyNM_001042494NP_0010359599990110
SLC12A7solute carrier family 12 (potassium/chloride transporter), member 7KCC4604879 NM_006598NP_0065891072320
SLC12A8solute carrier family 12, member 8CCC9611316 NM_024628NP_0789048456130
SLC12A9solute carrier family 12, member 9CIP1  NM_020246NP_0646315699660
SLC13A1solute carrier family 13 (sodium/sulfate symporter), member 1NAS1606193 NM_022444NP_0718896561114
SLC13A2solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2NaDC1604148 NM_003984NP_0039759058212
SLC13A3solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3NADC3606411 NM_022829NP_0737406484970
SLC13A4solute carrier family 13 (sodium/sulfate symporter), member 4SUT1604309 NM_012450NP_0365822626630
SLC13A5solute carrier family 13 (sodium-dependent citrate transporter), member 5NACT608305 NM_177550NP_80821828411140
SLC14A1solute carrier family 14 (urea transporter), member 1UT-B1613868Kidd blood polymorphism, Jk; JK-null variant; Jk-null variant, finnish typeNM_001128588NP_001122060656390
SLC14A2solute carrier family 14 (urea transporter), member 2UT2601611 NM_007163NP_009094817020
SLC15A1solute carrier family 15 (oligopeptide transporter), member 1PEPT1600544 NM_005073NP_0050646564119
SLC15A2solute carrier family 15 (oligopeptide transporter), member 2PEPT2602339 NM_021082NP_0665686565422
SLC15A3solute carrier family 15 (oligopeptide transporter), member 3SLC15A3610408 NM_016582NP_0576665129610
SLC15A4solute carrier family 15 (oligopeptide transporter), member 4SLC15A4  NM_145648NP_66362312126010
SLC15A5solute carrier family 15, member 5   NM_001170798NP_00116426972902510
SLC16A1solute carrier family 16 (monocarboxylate transporter), member 1MCT1600682 NM_003051NP_003042656631
SLC16A2solute carrier family 16, member 2 (thyroid hormone transporter)MCT8300095Monocarboxylate transporter 8 deficiencyNM_006517NP_006508656720
SLC16A3solute carrier family 16 (monocarboxylate transporter), member 3MCT3603877 NM_001042422NP_001035887912360
SLC16A4solute carrier family 16, member 4MCT4603878 NM_004696NP_004687912270
SLC16A5solute carrier family 16 (monocarboxylate transporter), member 5MCT5603879 NM_004695NP_004686912140
SLC16A6solute carrier family 16, member 6MCT6603880 NM_004694NP_004685912040
SLC16A7solute carrier family 16 (monocarboxylate transporter), member 7MCT2603654 NM_004731NP_004722919460
SLC16A8solute carrier family 16 (monocarboxylate transporter), member 8MCT3610409 NM_013356NP_0374882353910
SLC16A9solute carrier family 16, member 9SLC16A9614242 NM_194298NP_91927422096310
SLC16A10solute carrier family 16 (aromatic amino acid transporter), member 10TAT1607550 NM_018593NP_06106311724730
SLC16A11solute carrier family 16, member 11SLC16A11  NM_153357NP_69918816251520
SLC16A12solute carrier family 16, member 12 611910 NM_213606NP_99877138770030
SLC16A13solute carrier family 16, member 13SLC16A13  NM_201566NP_96386020123210
SLC16A14solute carrier family 16, member 14SLC16A14  NM_152527NP_68974015147340
SLC17A1solute carrier family 17 (organic anion transporter), member 1NAPI1182308 NM_005074NP_005065656831
SLC17A2solute carrier family 17, member 2NPT3611049 NM_005835NP_0058261024651
SLC17A3solute carrier family 17 (organic anion transporter), member 3NPT4611034 NM_001098486NP_0010919561078631
SLC17A4solute carrier family 17, member 4KAIA2138604216 NM_005495NP_0054861005031
SLC17A5solute carrier family 17 (acidic sugar transporter), member 5SLC17A5604322Salla disease; Infantile sialic acid storage disorderNM_012434NP_0365662650340
SLC17A6solute carrier family 17 (vesicular glutamate transporter), member 6VGLUT2607563 NM_020346NP_0650795708411
SLC17A7solute carrier family 17 (vesicular glutamate transporter), member 7VGLUT1605208 NM_020309NP_0647055703024
SLC17A8solute carrier family 17 (vesicular glutamate transporter), member 8VGLUT3607557 NM_139319NP_647480246213213
SLC17A9solute carrier family 17 (vesicular nucleotide transporter), member 9 612107 NM_022082NP_0713656391030
SLC18A1solute carrier family 18 (vesicular monoamine transporter), member 1VMAT1193002 NM_003053NP_0030446570413
SLC18A2solute carrier family 18 (vesicular monoamine transporter), member 2VMAT2193001 NM_003054NP_0030456571111
SLC18A3solute carrier family 18 (vesicular acetylcholine transporter), member 3VACHT600336 NM_003055NP_003046657214
SLC19A1solute carrier family 19 (folate transporter), member 1RFC1600424 NM_194255NP_919231657354
SLC19A2solute carrier family 19 (thiamine transporter), member 2TRMA603941Thiamine-responsive megaloblastic anemia syndromeNM_006996NP_0089271056021
SLC19A3solute carrier family 19 (thiamine transporter), member 3SLC19A3606152 NM_025243NP_0795198070460
SLC20A1solute carrier family 20 (phosphate transporter), member 1SLC20A1137570 NM_005415NP_005406657420
SLC20A2solute carrier family 20 (phosphate transporter), member 2SLC20A2158378 NM_006749NP_006740657560
SLC22A1solute carrier family 22 (organic cation transporter), member 1OCT1602607 NM_003057NP_0030486580611
SLC22A2solute carrier family 22 (organic cation transporter), member 2OCT2602608 NM_003058NP_0030496582113
SLC22A3solute carrier family 22 (organic cation transporter), member 3OCT3604842 NM_021977NP_0688126581317
SLC22A4solute carrier family 22 (organic cation/zwitterion transporter), member 4OCTN1604190Rheumatoid arthritis, susceptibility to; Crohn disease, susceptibility toNM_003059NP_0030506583112
SLC22A5solute carrier family 22 (organic cation/carnitine transporter), member 5OCTN2603377Carnitine deficiency, systemic primary; Crohn disease, susceptibility toNM_003060NP_0030516584314
SLC22A6solute carrier family 22 (organic anion transporter), member 6OAT1607582 NM_004790NP_0047819356412
SLC22A7solute carrier family 22 (organic anion transporter), member 7OAT2604995 NM_006672NP_00666310864413
SLC22A8solute carrier family 22 (organic anion transporter), member 8OAT3607581 NM_004254NP_0042459376711
SLC22A9solute carrier family 22 (organic anion transporter), member 9OAT4607579 NM_080866NP_543142114571210
SLC22A10solute carrier family 22, member 10 607580 NM_001039752NP_00103484138777523
SLC22A11solute carrier family 22 (organic anion/urate transporter), member 11OAT4607097 NM_018484NP_06095455867213
SLC22A12solute carrier family 22 (organic anion/urate transporter), member 12OAT4L607096Renal hypouricemiaNM_144585NP_653186116085129
SLC22A13solute carrier family 22 (organic anion/urate transporter), member 13OCTL1604047 NM_004256NP_004247939013
SLC22A14solute carrier family 22, member 14OCTL2604048 NM_004803NP_004794938943
SLC22A15solute carrier family 22, member 15FLIPT1608275 NM_018420NP_06089055356415
SLC22A16solute carrier family 22 (organic cation/carnitine transporter), member 16FLIPT2608276 NM_033125NP_1491168541348
SLC22A17solute carrier family 22, member 17BOCT611461 NM_020372NP_0651055131043
SLC22A18solute carrier family 22, member 18HET602631Breast cancer; Rhambdomyosarcoma; Lung cancer, somaticNM_002555NP_002546500243
SLC22A18ASsolute carrier family 22 (organic cation transporter), member 18 antisense 603240 NM_007105NP_009036500310
SLC22A20solute carrier family 22, member 20 611696 NM_001004326NP_00100432644004430
SLC22A23solute carrier family 22, member 23 611697 NM_015482NP_0562976302740
SLC22A24solute carrier family 22, member 24 611698 NM_001136506NP_00112997828323810
SLC22A25solute carrier family 22, member 25 610792 NM_199352NP_95538438760120
SLC23A1solute carrier family 23 (ascorbic acid transporter), member 1SVCT1603790 NM_005847NP_005838996340
SLC23A2solute carrier family 23 (ascorbic acid transporter), member 2SVCT2603791 NM_005116NP_005107996260
SLC23A3solute carrier family 23, member 3SVCT3  NM_144712NP_65331315129540
SLC23A4Psolute carrier family 23 (nucleobase transporters), member 4, pseudogene     64184200
SLC24A1solute carrier family 24 (sodium/potassium/calcium exchanger), member 1NCKX603617 NM_004727NP_004718918760
SLC24A2solute carrier family 24 (sodium/potassium/calcium exchanger), member 2NCKX2609838 NM_020344NP_0650772576950
SLC24A3solute carrier family 24 (sodium/potassium/calcium exchanger), member 3NCKX3609839 NM_020689NP_0657405741910
SLC24A4solute carrier family 24 (sodium/potassium/calcium exchanger), member 4NCKX4609840 NM_153646NP_70593212304150
SLC24A5solute carrier family 24 (sodium/potassium/calcium exchanger), member 5NCKX5609802 NM_205850NP_99532228365230
SLC25A1solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1CTP,SLC20A3190315 NM_005984NP_005975657620
SLC25A2solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 2ORNT2608157 NM_031947NP_1141538388410
SLC25A3solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 3PHC600370 NM_002635NP_002626525050
SLC25A4solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4ANT1103220Progressive external ophthalmoplegia with mitochondrial deletions, autosomal dominantNM_001151NP_00114229110
SLC25A5solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 5ANT2300150 NM_001152NP_00114329210
SLC25A6solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 6NCKX6300151 NM_001636NP_00162729310
SLC25A10solute carrier family 25 (mitochondrial carrier; dicarboxylate transporter), member 10DIC606794 NM_012140NP_036272146840
SLC25A11solute carrier family 25 (mitochondrial carrier; oxoglutarate carrier), member 11OGC,SLC20A4604165 NM_003562NP_003553840230
SLC25A12solute carrier family 25 (aspartate/glutamate carrier), member 12ARALAR603667 NM_003705NP_003696860430
SLC25A13solute carrier family 25 (aspartate/glutamate carrier), member 13ARALAR2603859Cirullinemia, type II, adult-onsetNM_014251NP_0550661016520
SLC25A14solute carrier family 25 (mitochondrial carrier, brain), member 14UCP5300242 NM_003951NP_003942901680
SLC25A15solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 15HHH603861HHH syndromeNM_014252NP_0550671016620
SLC25A16solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16GDA139080 NM_152707NP_689920803440
SLC25A17solute carrier family 25 (mitochondrial carrier; peroxisomal membrane protein, 34kDa), member 17PMP34606795 NM_006358NP_0063491047830
SLC25A18solute carrier family 25 (glutamate carrier), member 18GC2609303 NM_031481NP_1136698373380
SLC25A19solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19DNC606521Microcephaly, amish typeNM_001126121NP_0011195936038670
SLC25A20solute carrier family 25 (carnitine/acylcarnitine translocase), member 20CAC613698Carnitine-acylcarnitine translocase deficiencyNM_000387NP_00037878810
SLC25A21solute carrier family 25 (mitochondrial oxoadipate carrier), member 21ODC607571 NM_030631NP_0851348987420
SLC25A22solute carrier family 25 (mitochondrial carrier: glutamate), member 22GC1609302 NM_024698NP_0789747975130
SLC25A23solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23APC2608746 NM_024103NP_0770087908520
SLC25A24solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 24APC1608744 NM_013386NP_0375182995720
SLC25A25solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 25MCSC608745 NM_001006641NP_00100664211478960
SLC25A26solute carrier family 25 (S-adenosylmethionine carrier), member 26SAMC611037 NM_173471NP_77574211528620
SLC25A27solute carrier family 25, member 27UCP4613725 NM_004277NP_004268948160
SLC25A28solute carrier family 25 (mitochondrial iron transporter), member 28MRS3/4609767 NM_031212NP_1124898189450
SLC25A29solute carrier family 25 (mitochondrial carnitine/acylcarnitine carrier), member 29SLC25A29615064 NM_001039355NP_00103444412309650
SLC25A30solute carrier family 25, member 30SLC25A30610793 NM_001010875NP_00101087525351280
SLC25A31solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 31 610796 NM_031291NP_1125818344710
SLC25A32solute carrier family 25 (mitochondrial folate carrier), member 32 610815 NM_030780NP_1104078103410
SLC25A33solute carrier family 25 (pyrimidine nucleotide carrier), member 33 610816 NM_032315NP_1156918427520
SLC25A34solute carrier family 25, member 34 610817 NM_207348NP_99723128472320
SLC25A35solute carrier family 25, member 35 610818 NM_201520NP_95892839951270
SLC25A36solute carrier family 25 (pyrimidine nucleotide carrier ), member 36   NM_001104647NP_0010981175518640
SLC25A37solute carrier family 25 (mitochondrial iron transporter), member 37 610387 NM_016612NP_0576965131220
SLC25A38solute carrier family 25, member 38 610819 NM_017875NP_0603455497710
SLC25A39solute carrier family 25, member 39 610820 NM_016016NP_0571005162950
SLC25A40solute carrier family 25, member 40 610821 NM_018843NP_0613315597230
SLC25A41solute carrier family 25, member 41 610822 NM_173637NP_77590828442720
SLC25A42solute carrier family 25, member 42 610823 NM_178526NP_84862128443940
SLC25A43solute carrier family 25, member 43 300641 NM_145305NP_66034820342740
SLC25A44solute carrier family 25, member 44 610824 NM_014655NP_055470967330
SLC25A45solute carrier family 25, member 45 610825 NM_182556NP_87236228313060
SLC25A46solute carrier family 25, member 46 610826 NM_138773NP_6201289113730
SLC26A1solute carrier family 26 (anion exchanger), member 1SAT1610130 NM_022042NP_0713251086130
SLC26A2solute carrier family 26 (anion exchanger), member 2DTD606718Diastrophic dysplasia; Atelosteogenisi, type II; Achondrogensis, type IB; Diastrophic dyplasia, broad bone-platyspondylic variant; Epiphyseal dysplasia, multiple, 4NM_000112NP_000103183610
SLC26A3solute carrier family 26 (anion exchanger), member 3CLD126650Chloride diarrhea, congential, finnish type; Chloride diarrhea, congentialNM_000111NP_000102181110
SLC26A4solute carrier family 26 (anion exchanger), member 4PDS605646Pendred syndrome; Deafness, autosomal recessive 4; Enlarger vestibular aqueductNM_000441NP_000432517250
SLC26A5solute carrier family 26 (anion exchanger), member 5PRES604943 NM_198999NP_94535037561150
SLC26A6solute carrier family 26 (anion exchanger), member 6SLC26A6610068 NM_022911NP_0750626501070
SLC26A7solute carrier family 26 (anion exchanger), member 7SLC26A7608479 NM_052832NP_43989711511150
SLC26A8solute carrier family 26 (anion exchanger), member 8TAT1608480 NM_052961NP_44319311636930
SLC26A9solute carrier family 26 (anion exchanger), member 9SLC26A9608481 NM_052934NP_44316611501920
SLC26A10solute carrier family 26, member 10SLC26A10  NM_133489NP_5979966501210
SLC26A11solute carrier family 26 (anion exchanger), member 11SLC26A11610117 NM_173626NP_77589728412950
SLC27A1solute carrier family 27 (fatty acid transporter), member 1FATP600691 NM_198580NP_94098237649710
SLC27A2solute carrier family 27 (fatty acid transporter), member 2FATP2603247 NM_003645NP_0036361100120
SLC27A3solute carrier family 27 (fatty acid transporter), member 3FATP3604193 NM_024330NP_0773061100050
SLC27A4solute carrier family 27 (fatty acid transporter), member 4FATP4604194 NM_005094NP_0050851099920
SLC27A5solute carrier family 27 (fatty acid transporter), member 5FATP5603314 NM_012254NP_0363861099830
SLC27A6solute carrier family 27 (fatty acid transporter), member 6FATP6604196 NM_001017372NP_0010173722896570
SLC28A1solute carrier family 28 (concentrative nucleoside transporter), member 1CNT1606207 NM_004213NP_00420491541017
SLC28A2solute carrier family 28 (concentrative nucleoside transporter), member 2SPNT1606208 NM_004212NP_0042039153115
SLC28A3solute carrier family 28 (concentrative nucleoside transporter), member 3CNT3608269 NM_022127NP_07141064078219
SLC29A1solute carrier family 29 (equilibrative nucleoside transporter), member 1ENT1602193 NM_001078174NP_00107164220301312
SLC29A2solute carrier family 29 (equilibrative nucleoside transporter), member 2ENT2602110 NM_001532NP_0015233177214
SLC29A3solute carrier family 29 (equilibrative nucleoside transporter), member 3ENT3612373 NM_018344NP_0608145531523
SLC29A4solute carrier family 29 (equilibrative nucleoside transporter), member 4ENT4609149 NM_001040661NP_00103575122296240
SLC30A1solute carrier family 30 (zinc transporter), member 1ZNT1609521 NM_021194NP_067017777910
SLC30A2solute carrier family 30 (zinc transporter), member 2ZNT2609617 NM_001004434NP_001004434778030
SLC30A3solute carrier family 30 (zinc transporter), member 3ZNT3602878 NM_003459NP_003450778160
SLC30A4solute carrier family 30 (zinc transporter), member 4ZNT4602095 NM_013309NP_037441778220
SLC30A5solute carrier family 30 (zinc transporter), member 5ZNT5607819 NM_022902NP_0750536492440
SLC30A6solute carrier family 30 (zinc transporter), member 6ZNT6611148 NM_017964NP_0604345567650
SLC30A7solute carrier family 30 (zinc transporter), member 7ZNT7611149 NM_133496NP_59800314886740
SLC30A8solute carrier family 30 (zinc transporter), member 8ZNT-8611145 NM_173851NP_77625016902660
SLC30A9solute carrier family 30 (zinc transporter), member 9ZNT9604604 NM_006345NP_0063361046330
SLC30A10solute carrier family 30, member 10ZNT8,ZnT-10611146 NM_018713NP_0611835553210
SLC31A1solute carrier family 31 (copper transporter), member 1CTR1603085 NM_001859NP_001850131715
SLC31A2solute carrier family 31 (copper transporter), member 2CTR2603088 NM_001860NP_001851131810
SLC32A1solute carrier family 32 (GABA vesicular transporter), member 1VGAT  NM_080552NP_54211914067911
SLC33A1solute carrier family 33 (acetyl-CoA transporter), member 1AT1, ACATN603690 NM_004733NP_004724919720
SLC34A1solute carrier family 34 (type II sodium/phosphate contransporter), member 1SLC34A1182309Urolithiasis, hypophosphatemic; osteoporosis, hypophosphatemicNM_003052NP_003043656960
SLC34A2solute carrier family 34 (type II sodium/phosphate contransporter), member 2SLC34A2604217 NM_006424NP_0064151056850
SLC34A3solute carrier family 34 (type II sodium/phosphate contransporter), member 3SLC34A3609826 NM_080877NP_54315314268030
SLC35A1solute carrier family 35 (CMP-sialic acid transporter), member A1CST605634 NM_006416NP_0064071055950
SLC35A2solute carrier family 35 (UDP-galactose transporter), member A2UGT314375 NM_001032289NP_001027460735590
SLC35A3solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member A3SLC35A3605632 NM_012243NP_0363752344360
SLC35A4solute carrier family 35, member A4MGC2541  NM_080670NP_54240111382910
SLC35A5solute carrier family 35, member A5FLJ20730  NM_017945NP_0604155503210
SLC35B1solute carrier family 35, member B1 610790 NM_005827NP_0058181023740
SLC35B2solute carrier family 35 (adenosine 3'-phospho 5'-phosphosulfate transporter), member B2 610788 NM_178148NP_83536134773440
SLC35B3solute carrier family 35 (adenosine 3'-phospho 5'-phosphosulfate transporter), member B3 610845 NM_015948NP_0570325100070
SLC35B4solute carrier family 35 (UDP-xylose/UDP-N-acetylglucosamine transporter), member B4 610923 NM_032826NP_1162158491210
SLC35C1solute carrier family 35 (GDP-fucose transporter), member C1 605881 NM_018389NP_0608595534350
SLC35C2solute carrier family 35 (GDP-fucose transporter), member C2   NM_015945NP_0570295100680
SLC35D1solute carrier family 35 (UDP-GlcA/UDP-GalNAc transporter), member D1 610804 NM_015139NP_0559542316920
SLC35D2solute carrier family 35 (UDP-GlcNAc/UDP-glucose transporter), member D2 609182 NM_007001NP_0089321104670
SLC35D3solute carrier family 35, member D3 612519 NM_001008783NP_00100878334014610
SLC35E1solute carrier family 35, member E1   NM_024881NP_0791577993910
SLC35E2solute carrier family 35, member E2   NM_182838NP_878258990640
SLC35E3solute carrier family 35, member E3   NM_018656NP_0611265550820
SLC35F1solute carrier family 35, member F1   NM_001029858NP_00102502922255320
SLC35F2solute carrier family 35, member F2   NM_017515NP_0599855473340
SLC35F3solute carrier family 35, member F3   NM_173508NP_77577914864120
SLC35F4solute carrier family 35, member F4   NM_001206920NP_00119384934188030
SLC35F5solute carrier family 35, member F5   NM_025181NP_0794578025540
SLC36A1solute carrier family 36 (proton/amino acid symporter), member 1SLC36A1606561 NM_078483NP_51096820635840
SLC36A2solute carrier family 36 (proton/amino acid symporter), member 2PAT2608331 NM_181776NP_86144115320130
SLC36A3solute carrier family 36, member 3PAT3608332 NM_181774NP_86143928564120
SLC36A4solute carrier family 36 (proton/amino acid symporter), member 4PAT4613760 NM_152313NP_68952612010340
SLC37A1solute carrier family 37 (glucose-6-phosphate transporter), member 1G3PP608094 NM_018964NP_0618375402050
SLC37A2solute carrier family 37 (glucose-6-phosphate transporter), member 2FLJ00171  NM_198277NP_93801821985520
SLC37A3solute carrier family 37, member 3MGC32939  NM_032295NP_1156718425530
SLC37A4solute carrier family 37 (glucose-6-phosphate transporter), member 4SLC37A4602671Glycogen storage disease Ib; Glycogen storage disease IcNM_001467NP_001458254270
SLC38A1solute carrier family 38, member 1ATA1608490 NM_001077484NP_0010709528153960
SLC38A2solute carrier family 38, member 2SAT2605180 NM_018976NP_0618495440720
SLC38A3solute carrier family 38, member 3G17604437 NM_006841NP_0068321099110
SLC38A4solute carrier family 38, member 4ATA3608065 NM_018018NP_0604885508940
SLC38A5solute carrier family 38, member 5SN2300649 NM_033518NP_27705392745110
SLC38A6solute carrier family 38, member 6NAT-1  NM_153811NP_72251814538920
SLC38A7solute carrier family 38, member 7 614236 NM_018231NP_0607015523820
SLC38A8solute carrier family 38, member 8   NM_001080442NP_00107391114616710
SLC38A9solute carrier family 38, member 9   NM_173514NP_77578515312930
SLC38A10solute carrier family 38, member 10   NM_138570NP_61263712456530
SLC38A11solute carrier family 38, member 11   NM_173512NP_77578315125830
SLC39A1solute carrier family 39 (zinc transporter), member 1ZIP1604740 NM_014437NP_0552522717360
SLC39A2solute carrier family 39 (zinc transporter), member 2ZIP2612166 NM_014579NP_0553942998620
SLC39A3solute carrier family 39 (zinc transporter), member 3ZIP3612168 NM_144564NP_6531652998530
SLC39A4solute carrier family 39 (zinc transporter), member 4ZIP4607059Acrodermatitis ehteropathicaNM_017767NP_0602375563030
SLC39A5solute carrier family 39 (zinc transporter), member 5ZIP5608730 NM_173596NP_77586728337530
SLC39A6solute carrier family 39 (zinc transporter), member 6LIV-1608731 NM_001099406NP_0010928762580020
SLC39A7solute carrier family 39 (zinc transporter), member 7KE4601416 NM_001077516NP_001070984792280
SLC39A8solute carrier family 39 (zinc transporter), member 8LZT-Hs6608732 NM_022154NP_0714376411650
SLC39A9solute carrier family 39, member 9FLJ11274  NM_018375NP_0608455533460
SLC39A10solute carrier family 39 (zinc transporter), member 10LZT-Hs2608733 NM_001127257NP_0011207295718160
SLC39A11solute carrier family 39, member 11C17orf26  NM_139177NP_63191620126650
SLC39A12solute carrier family 39 (zinc transporter), member 12FLJ30499608734 NM_152725NP_68993822107440
SLC39A13solute carrier family 39 (zinc transporter), member 13FLJ25785608735 NM_001128225NP_0011216979125260
SLC39A14solute carrier family 39 (zinc transporter), member 14LZT-Hs4608736 NM_001128431NP_0011219032351690
SLC40A1solute carrier family 40 (iron-regulated transporter), member 1IREG1604653Hemochromatosis, type 4NM_014585NP_0554003006139
SLC41A1solute carrier family 41 (magnesium transporter), member 1MgtE610801 NM_173854NP_77625325442820
SLC41A2solute carrier family 41 (magnesium transporter), member 2SLC41A1-L1610802 NM_032148NP_1155248410260
SLC41A3solute carrier family 41, member 3SLC41A1-L2610803 NM_001008485NP_00100848554946130
SLC43A1solute carrier family 43 (amino acid system L transporter), member 1 603733 NM_003627NP_003618850140
SLC43A2solute carrier family 43 (amino acid system L transporter), member 2 610791 NM_152346NP_68955912493540
SLC43A3solute carrier family 43, member 3   NM_017611NP_06008129015190
SLC44A1solute carrier family 44 (choline transporter), member 1 606105 NM_080546NP_5368562344640
SLC44A2solute carrier family 44 (choline transporter), member 2 606106 NM_020428NP_0651615715350
SLC44A3solute carrier family 44, member 3   NM_152369NP_689582126969120
SLC44A4solute carrier family 44, member 4 606107 NM_025257NP_0795338073630
SLC44A5solute carrier family 44, member 5   NM_152697NP_68991020496250
SLC45A1solute carrier family 45, member 1 605763 NM_001080397NP_0010738665065120
SLC45A2solute carrier family 45, member 2 606202 NM_016180NP_0572645115130
SLC45A3solute carrier family 45, member 3 605097 NM_033102NP_1490938541460
SLC45A4solute carrier family 45, member 4   NM_001080431NP_0010739005721030
SLC46A1solute carrier family 46 (folate transporter), member 1 611672 NM_080669NP_54240011323530
SLC46A2solute carrier family 46, member 2 608956 NM_033051NP_1490405786420
SLC46A3solute carrier family 46, member 3   NM_181785NP_86145028353730
SLC47A1solute carrier family 47 (multidrug and toxin extrusion), member 1MATE1609832 NM_018242NP_06071255244620
SLC47A2solute carrier family 47 (multidrug and toxin extrusion), member 2MATE2-K609833 NM_001099646NP_001093116146802616
SLCO1A2solute carrier organic anion transporter family, member 1A2OATP1A2602883 NM_021094NP_0665806579718
SLCO1B1solute carrier organic anion transporter family, member 1B1OATP1B1604843 NM_006446NP_00643710599119
SLCO1B3solute carrier organic anion transporter family, member 1B3OATP1B3605495 NM_019844NP_06281828234212
SLCO1C1solute carrier organic anion transporter family, member 1C1OATPF613389 NM_017435NP_0591315391981
SLCO2A1solute carrier organic anion transporter family, member 2A1SLCO2A1601460 NM_005630NP_005621657810
SLCO2B1solute carrier organic anion transporter family, member 2B1OATPB604988 NM_007256NP_00918711309414
SLCO3A1solute carrier organic anion transporter family, member 3A1OATPD612435 NM_013272NP_0374042823257
SLCO4A1solute carrier organic anion transporter family, member 4A1OATPE612436 NM_016354NP_0574382823120
SLCO4C1solute carrier organic anion transporter family, member 4C1OATPH609013 NM_180991NP_85132235318911
SLCO5A1solute carrier organic anion transporter family, member 5A1OATPJ613543 NM_030958NP_1122208179651
SLCO6A1solute carrier organic anion transporter family, member 6A1OATPY613365 NM_173488NP_77575913348261
TAP1transporter 1, ATP-binding cassette, sub-family B (MDR/TAP)TAP1170260Peptide transporter psf1 polymorhpism; Tap1 deficiency, somaticNM_000593NP_000584689091
TAP2transporter 2, ATP-binding cassette, sub-family B (MDR/TAP)TAP2170261Peptide transporter psf2 polymorphism; Bare lymphocyte syndrome, type 1; Wegener-like granulomatosisNM_000544NP_0005356891131
TPH2tryptophan hydroxylase 2 607478 NM_173353NP_77548912127820
UCP1uncoupling protein 1 (mitochondrial, proton carrier)UCP1113730UCP1 polymorphismNM_021833NP_068605735020
UCP2uncoupling protein 2 (mitochondrial, proton carrier)UCP2601693Obesity, susceptibility toNM_003355NP_003346735110
UCP3uncoupling protein 3 (mitochondrial, proton carrier)SLC25A9602044UCP3 polymorphism G/A; Obesity, severe, and type II diabetes; UCP3 polymprphism, exon6 splice donor junctionNM_003356NP_003347735220