UCSF Pharmacogenetics of Membrane Transporters
Gene View
Common Name:None
HGNC Symbol:RHCG
HGNC Description:Rh family, C glycoprotein
HGNC ID:18140
Superfamily:SLC
Chromosome:Chr.15(-): 90014638-90039799 GRCh37
Location:15q25
OMIM:605381
OMIM Phenotype:None
Accessions:None
Nucleotide RefSeq:NM_016321
Protein RefSeq:NP_057405
Entrez:51458
Ensembl:ENSG00000140519
Isoforms:1
Evidence:None
Tissues:None
Type:protein-coding
Sets:None
PharmGKB ID:
HPRD ID:16102
Substrates:None
Trivial Names:RHGK, PDRC2, C15orf6, SLC42A3
Transcripts:NM_016321.1 [Chr.15(-): 90014638-90039799 GRCh37]
ENST00000268122 [Chr.15(-): 90014638-90039844 GRCh37]
ENST00000544600 [Chr.15(-): 89998680-90039814 GRCh37]
ENST00000558030 [Chr.15(-): 90014988-90039813 GRCh37]
ENST00000558184 [Chr.15(-): 90020959-90039820 GRCh37]
ENST00000558360 [Chr.15(-): 90014676-90022661 GRCh37]
ENST00000559638 [Chr.15(-): 90021030-90022967 GRCh37]
ENST00000560081 [Chr.15(-): 90014629-90039802 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 RHCG.

Variant Data

View all PMT variants for RHCG on UCSC Genome Browser
Showing SNP features for transcript: NM_016321  
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.