UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:GDA
HGNC Symbol:SLC25A16
HGNC Description:solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16
HGNC ID:10986
Superfamily:SLC
Chromosome:Chr.10(-): 70242090-70287280 GRCh37
Location:10q21.3
OMIM:139080
OMIM Phenotype:None
Accessions:BC030266,BE280946,BU618210
Nucleotide RefSeq:NM_152707
Protein RefSeq:NP_689920
Entrez:8034
Ensembl:ENSG00000122912
Isoforms:4
Evidence:None
Tissues:None
Type:protein-coding
Sets:0
PharmGKB ID:PA35862
HPRD ID:00740
Substrates:None
Trivial Names:GDA, GDC, ML7, hML7, HGT.1, D10S105E
Transcripts:NM_152707.3 [Chr.10(-): 70242090-70287280 GRCh37]
XM_005270181.1 [Chr.10(-): 70242090-70287280 GRCh37]
XM_005270182.1 [Chr.10(-): 70242090-70287278 GRCh37]
XM_005270183.1 [Chr.10(-): 70242090-70256538 GRCh37]
ENST00000265870 [Chr.10(-): 70242776-70277975 GRCh37]
ENST00000439904 [Chr.10(-): 70237756-70240521 GRCh37]
ENST00000474927 [Chr.10(-): 70252931-70266362 GRCh37]
ENST00000491102 [Chr.10(-): 70266384-70287173 GRCh37]
ENST00000493963 [Chr.10(-): 70243232-70287195 GRCh37]
ENST00000539557 [Chr.10(-): 70242767-70287173 GRCh37]
ENST00000608053 [Chr.10(-): 70246831-70248347 GRCh37]
ENST00000609923 [Chr.10(-): 70237758-70287231 GRCh37]
Annotation History:View Events (25)

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.

Tissues:
Expression values:
No expression data exists for SLC25A16.

Variant Data

View all PMT variants for SLC25A16 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: TOPO2 image is not available.