UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:None
HGNC Description:Rh family, B glycoprotein (gene/pseudogene)
HGNC ID:14572
Chromosome:Chr.1(+): 156338980-156355013 GRCh37
OMIM Phenotype:None
Nucleotide RefSeq:NM_020407
Protein RefSeq:NP_065140
PharmGKB ID:
HPRD ID:06152
Trivial Names:SLC42A2
Transcripts:NM_020407.4 [Chr.1(+): 156338980-156355013 GRCh37]
NM_001256396.1 [Chr.1(+): 156338980-156355013 GRCh37]
NM_001256395.1 [Chr.1(+): 156338980-156355013 GRCh37]
ENST00000255013 [Chr.1(+): 156339003-156355009 GRCh37]
ENST00000368245 [Chr.1(+): 156339042-156355011 GRCh37]
ENST00000368246 [Chr.1(+): 156339003-156355009 GRCh37]
ENST00000368247 [Chr.1(+): 156339003-156355011 GRCh37]
ENST00000368249 [Chr.1(+): 156339003-156355011 GRCh37]
ENST00000400992 [Chr.1(+): 156339003-156355009 GRCh37]
ENST00000446171 [Chr.1(+): 156339003-156355011 GRCh37]
ENST00000451864 [Chr.1(+): 156339003-156354329 GRCh37]
ENST00000466013 [Chr.1(+): 156339031-156355005 GRCh37]
ENST00000467375 [Chr.1(+): 156339003-156341670 GRCh37]
ENST00000477000 [Chr.1(+): 156352104-156354395 GRCh37]
ENST00000494874 [Chr.1(+): 156351934-156354676 GRCh37]
ENST00000537040 [Chr.1(+): 156339003-156352541 GRCh37]
ENST00000544720 [Chr.1(+): 156339003-156354940 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.

Expression values:
No expression data exists for RHBG.

Variant Data

View all PMT variants for RHBG 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.