UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:GLUT14
HGNC Symbol:SLC2A14
HGNC Description:solute carrier family 2 (facilitated glucose transporter), member 14
HGNC ID:18301
Chromosome:Chr.12(-): 7965110-8043792 GRCh37
OMIM Phenotype:None
Nucleotide RefSeq:NM_153449
Protein RefSeq:NP_703150
Evidence:Substrate In Vitro Evidence: Until now GLUT14 was thought to be a pseudogene. It is likely resulted from a duplication of GLUT3. Wu,X. and Freeze,H.H. GLUT14, a duplicon of GLUT3, is specifically expressed in testis as alternative splice forms. Genomics 80 (6), 553-557 (2002). Tissue Distribution Evidence: GLUT14 has two alternatively spliced forms; the shorter form and the longer form. In contrast to the expression of GLUT3 in many tissues, both isoforms of GLUT14 are specifically expressed in testis. (RT-PCR and Northern blotting) Wu,X. and Freeze,H.H. GLUT14, a duplicon of GLUT3, is specifically expressed in testis as alternative splice forms. Genomics 80 (6), 553-557 (2002).
PharmGKB ID:PA134885058
HPRD ID:11573
Substrates:pseudogene, N/A
Trivial Names:GLUT14, SLC2A3P3
Transcripts:NM_153449.2 [Chr.12(-): 7966397-8025495 GRCh37]
XM_005253312.1 [Chr.12(-): 7965110-8043792 GRCh37]
XM_005253317.1 [Chr.12(-): 7965110-8025954 GRCh37]
XM_005253315.1 [Chr.12(-): 7965110-8025522 GRCh37]
XM_005253314.1 [Chr.12(-): 7965110-8025512 GRCh37]
XM_005253316.1 [Chr.12(-): 7965110-8025420 GRCh37]
XM_005253313.1 [Chr.12(-): 7965110-8024538 GRCh37]
XM_005253318.1 [Chr.12(-): 7965115-8025448 GRCh37]
ENST00000340749 [Chr.12(-): 7965108-8025448 GRCh37]
ENST00000396589 [Chr.12(-): 7966397-8025635 GRCh37]
ENST00000431042 [Chr.12(-): 7965115-8025512 GRCh37]
ENST00000535266 [Chr.12(-): 7982584-8025710 GRCh37]
ENST00000535295 [Chr.12(-): 7966616-8025448 GRCh37]
ENST00000535344 [Chr.12(-): 7982452-8025398 GRCh37]
ENST00000535383 [Chr.12(-): 7984330-8026080 GRCh37]
ENST00000535587 [Chr.12(-): 7985362-8025476 GRCh37]
ENST00000536594 [Chr.12(-): 7984245-8025457 GRCh37]
ENST00000537557 [Chr.12(-): 7982520-8025479 GRCh37]
ENST00000539234 [Chr.12(-): 8016033-8025448 GRCh37]
ENST00000539738 [Chr.12(-): 7983860-7985361 GRCh37]
ENST00000539924 [Chr.12(-): 7966668-8043744 GRCh37]
ENST00000542505 [Chr.12(-): 7966125-8025847 GRCh37]
ENST00000542546 [Chr.12(-): 7966616-7985412 GRCh37]
ENST00000542782 [Chr.12(-): 7982418-8025623 GRCh37]
ENST00000542916 [Chr.12(-): 7984219-8024976 GRCh37]
ENST00000543909 [Chr.12(-): 7965110-8025420 GRCh37]
ENST00000544749 [Chr.12(-): 8023446-8025460 GRCh37]
ENST00000546234 [Chr.12(-): 7982368-8025470 GRCh37]
Annotation History:View Events (62)

GTEx Expression by Gene and Transcript

The heat map summarizes relative expression by tissue type at two levels of tissue detail, e.g., 'Brain' and 'Brain - Amygdala'. Choose among four calculated expression values, including mean and median RPKM values, and quantile normalized (QN) distributions of these values. (Note that differences between some distributions are subtle.) The coloring is relative to the mean of all displayed values. All values are log base 2. (See also PMT GTEx Expression Plotting.) Click on a transcript or tissue to resort the data.

Expression values:
No expression data exists for SLC2A14.

Variant Data

View all PMT variants for SLC2A14 on UCSC Genome Browser
Showing SNP features for transcript:   
1000 Genomes  

20141104 phase 3 variant call set of the 20130502 sequence freeze and alignments for SNPs and short indels (indels > 255 and structural variants are not included here). This variant set contains 2504 individuals from 26 populations (mouse over population column heading for population sizes).
Showing gene variants in regions defined by NCBI RefSeq exons, putative promoter, and PMT resequencing assays.
Note: Frequencies are calculated directly from reported genotypes and may vary from consensus frequencies reported by the 1000 Genomes project, which relied on additional data and the GATK tool Variant Quality Score Recalibrator.
dbSNP build 142.
Array availability: I - found on Illumina Human1M-Duo BeadChip (2011-04-21)  A - found on Affymetrix Genome-Wide SNP Array 6.0 (2011-06-21)  
Download the SNP table data as a tab-delimited file.

Transmembrane prediction:

Non-synonymous amino acid changes shown in red, indels (insertions and deletions) in blue, and synonymous changes in green. Exon(s) indicated by black outlines.