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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: RHCG ENSG00000140519

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Description

Rh family, C glycoprotein [Source:HGNC Symbol;Acc:18140]

Gene Synonyms

C15orf6, CDRC2, PDRC2, RHGK, SLC42A3

Location

Chromosome 15: 89,998,680-90,039,844 reverse strand.

GRCh37:CM000677.1

About this gene

This gene has 7 transcripts (splice variants) and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000268122.4	RHCG-001	1982	479aa	ENSP00000268122.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS10351	Q9UBD6	NM_016321.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000544600.1	RHCG-201	1748	445aa	ENSP00000438123.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		F5H0A6	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000558360.1	RHCG-005	1014	237aa	ENSP00000453496.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		-	-	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENST00000560081.1	RHCG-003	1862	331aa	ENSP00000453588.1	Nonsense mediated decay		H0YMF8	-	-
ENST00000558030.1	RHCG-007	1405	233aa	ENSP00000452899.1	Nonsense mediated decay		H0YKQ3	-	-
ENST00000558184.1	RHCG-002	1388	136aa	ENSP00000453716.1	Nonsense mediated decay		H0YMS1	-	-
ENST00000559638.1	RHCG-004	591	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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