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

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Gene: ARHGAP12 ENSBTAG00000012677

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Description

Rho GTPase activating protein 12 [Source:VGNC Symbol;Acc:VGNC:26075]

Location

Primary_assembly 13: 33,421,151-33,538,437 forward strand.

ARS-UCD1.3:CM008180.2

About this gene

This gene has 4 transcripts (splice variants), 283 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000085011.2	ARHGAP12-201	4163	856aa	ENSBTAP00000070520.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MH24	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,
ENSBTAT00000085714.2	ARHGAP12-202	4130	847aa	ENSBTAP00000066998.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M6Y9	-
ENSBTAT00000086884.2	ARHGAP12-203	4115	842aa	ENSBTAP00000069521.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M6Y9	-
ENSBTAT00000016846.6	ARHGAP12-204	4097	834aa	ENSBTAP00000016846.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6QPU2	APPRIS P4: Where the APPRIS core modules are unable to choose a clear principal CDS and there is more than one variant with a distinct (but consecutive) CCDS identifiers, APPRIS selects the longest CCDS isoform 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 P4,

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Summary

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