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

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Gene: arhgap36 ENSDARG00000059672

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Description

Rho GTPase activating protein 36 [Source:ZFIN;Acc:ZDB-GENE-060616-298]

Gene Synonyms

arhgap6, zgc:136763

Location

Chromosome 7: 51,364,290-51,461,664 reverse strand.

GRCz11:CM002891.2

About this gene

This gene has 4 transcripts (splice variants), 186 orthologues and 1 paralogue.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000083189.6	arhgap36-201	2736	630aa	ENSDARP00000077624.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q1ECW3	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 ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. 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 ALT2,
ENSDART00000193947.1	arhgap36-204	3158	668aa	ENSDARP00000146614.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2R8PZE5	APPRIS P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as the principal variant. 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 P5,
ENSDART00000146385.3	arhgap36-202	985	158aa	ENSDARP00000143189.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1L1QZR2	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,
ENSDART00000174328.2	arhgap36-203	946	196aa	ENSDARP00000143028.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A1L1QZB2	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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