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

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Gene: rhogb ENSDARG00000004301

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Description

ras homolog family member Gb [Source:ZFIN;Acc:ZDB-GENE-030131-8877]

Location

Chromosome 21: 30,937,690-30,951,909 forward strand.

GRCz11:CM002905.2

About this gene

This gene has 2 transcripts (splice variants), 203 orthologues and 42 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000022562.7	rhogb-201	1957	191aa	ENSDARP00000027635.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q803F2	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,
ENSDART00000187572.1	rhogb-202	579	191aa	ENSDARP00000156556.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q803F2	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,

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Summary

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