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

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Gene: RHOC ENSPTRG00000001112

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Description

ras homolog family member C [Source:VGNC Symbol;Acc:VGNC:1493]

Location

Chromosome 1: 123,386,604-123,395,808 forward strand.

Pan_tro_3.0:CM000314.3

About this gene

This gene has 3 transcripts (splice variants), 93 orthologues and 29 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000091770.1	RHOC-203	591	196aa	ENSPTRP00000071746.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3S4I6	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,
ENSPTRT00000002089.4	RHOC-201	2247	193aa	ENSPTRP00000001916.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2PZP2	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,
ENSPTRT00000097255.1	RHOC-202	390	129aa	ENSPTRP00000093712.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3TXI5	-

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Summary

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