Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

Configure this page

Share this page

Bookmark this page

.

Gene: Rhcg ENSRNOG00000015526

.

Description

Rh family, C glycoprotein [Source:RGD Symbol;Acc:727859]

Location

Primary_assembly 1: 142,941,048-142,965,376 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 2 transcripts (splice variants), 293 orthologues, 3 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000021109.6	Rhcg-201	2150	520aa	ENSRNOP00000021109.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6JC59 F1M794	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,
ENSRNOT00000098852.2	Rhcg-202	1837	464aa	ENSRNOP00000078063.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y844	-

.

Summary

.

.