Gene: Arhgap32 ENSRNOG00000008709

Description

Rho GTPase activating protein 32 [Source:RGD Symbol;Acc:1305267]

Gene Synonyms

Grit, Rics, p250GAP

Location

Primary_assembly 8: 30,421,515-30,678,454 forward strand.

mRatBN7.2:CM026981.1

About this gene

This gene has 4 transcripts (splice variants), 203 orthologues, 3 paralogues and is associated with 7 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000011589.7	Arhgap32-201	6599	2101aa	ENSRNOP00000011589.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MAK3	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,
ENSRNOT00000100925.1	Arhgap32-203	6769	2046aa	ENSRNOP00000077564.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y6H2	-
ENSRNOT00000119263.1	Arhgap32-204	6506	2070aa	ENSRNOP00000088168.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GFW8	-
ENSRNOT00000099034.1	Arhgap32-202	6399	2061aa	ENSRNOP00000089744.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GIC6	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,