UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:ANT2
HGNC Symbol:SLC25A5
HGNC Description:solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 5
HGNC ID:10991
Superfamily:SLC
Chromosome:Chr.X(+): 118602363-118605359 GRCh37
Location:Xq24
OMIM:300150
OMIM Phenotype:None
Accessions:M57424
Nucleotide RefSeq:NM_001152
Protein RefSeq:NP_001143
Entrez:292
Ensembl:ENSG00000005022
Isoforms:1
Evidence:None
Tissues:None
Type:protein-coding
Sets:0
PharmGKB ID:PA35867
HPRD ID:02147
Substrates:None
Trivial Names:T2, T3, 2F1, AAC2, ANT2
Transcripts:NM_001152.4 [Chr.X(+): 118602363-118605359 GRCh37]
ENST00000317881 [Chr.X(+): 118602363-118605282 GRCh37]
ENST00000460013 [Chr.X(+): 118603240-118604903 GRCh37]
ENST00000463551 [Chr.X(+): 118604225-118605044 GRCh37]
ENST00000475354 [Chr.X(+): 118602385-118604118 GRCh37]

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 SLC25A5.

Variant Data

View all PMT variants for SLC25A5 on UCSC Genome Browser
Showing SNP features for transcript: NM_001152  
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.