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

Configure this page

Share this page

Bookmark this page

.

Gene: rhogc ENSDARG00000028401

.

Description

ras homolog gene family, member Gc [Source:ZFIN;Acc:ZDB-GENE-030131-3402]

Location

Chromosome 5: 36,595,149-36,597,636 reverse strand.

GRCz11:CM002889.2

About this gene

This gene has 2 transcripts (splice variants), 145 orthologues and 42 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000122098.3	rhogc-202	2174	191aa	ENSDARP00000106006.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q803L7	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,
ENSDART00000031270.5	rhogc-201	2135	191aa	ENSDARP00000035977.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q803L7	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,

.

Summary

.

.