UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:SLC41A1-L1
HGNC Symbol:SLC41A2
HGNC Description:solute carrier family 41 (magnesium transporter), member 2
HGNC ID:31045
Chromosome:Chr.12(-): 105196331-105352476 GRCh37
OMIM Phenotype:None
Nucleotide RefSeq:NM_032148
Protein RefSeq:NP_115524
PharmGKB ID:PA134931432
HPRD ID:15389
Trivial Names:SLC41A1-L1
Transcripts:NM_032148.3 [Chr.12(-): 105197275-105322472 GRCh37]
XM_005269177.1 [Chr.12(-): 105196331-105352476 GRCh37]
XM_005269176.1 [Chr.12(-): 105196331-105352071 GRCh37]
XM_005269178.1 [Chr.12(-): 105196331-105352068 GRCh37]
XM_005269179.1 [Chr.12(-): 105196331-105345306 GRCh37]
XM_005269180.1 [Chr.12(-): 105227804-105352071 GRCh37]
ENST00000258538 [Chr.12(-): 105196331-105322433 GRCh37]
ENST00000411411 [Chr.12(-): 105321940-105345306 GRCh37]
ENST00000415674 [Chr.12(-): 105321875-105352071 GRCh37]
ENST00000417469 [Chr.12(-): 105322168-105352476 GRCh37]
ENST00000424946 [Chr.12(-): 105322089-105352071 GRCh37]
ENST00000432951 [Chr.12(-): 105322270-105352066 GRCh37]
ENST00000433540 [Chr.12(-): 105322078-105352097 GRCh37]
ENST00000437220 [Chr.12(-): 105282811-105321980 GRCh37]
ENST00000449866 [Chr.12(-): 105322022-105352522 GRCh37]
ENST00000549713 [Chr.12(-): 105198753-105227957 GRCh37]
Annotation History:View Events (44)

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 SLC41A2.

Variant Data

View all PMT variants for SLC41A2 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.