Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: Arhgap12 ENSRNOG00000017791

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Description

Rho GTPase activating protein 12 [Source:RGD Symbol;Acc:1310017]

Gene Synonyms

LOC307016

Location

Primary_assembly 17: 56,284,286-56,397,563 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 4 transcripts (splice variants), 201 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000097647.2	Arhgap12-203	4965	843aa	ENSRNOP00000094054.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AN18	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,
ENSRNOT00000024022.8	Arhgap12-201	4950	838aa	ENSRNOP00000024022.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZDI5	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be 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 P2,
ENSRNOT00000084919.3	Arhgap12-202	4062	813aa	ENSRNOP00000072043.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K1Z2	APPRIS ALT1: 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 is conserved in at least 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 ALT1,
ENSRNOT00000117680.2	Arhgap12-204	4026	796aa	ENSRNOP00000092878.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AW83	-

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Summary

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