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: ARHGAP10 ENSBTAG00000002531

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Description

Rho GTPase activating protein 10 [Source:VGNC Symbol;Acc:VGNC:26074]

Location

Primary_assembly 17: 10,027,382-10,414,404 reverse strand.

ARS-UCD1.3:CM008184.2

About this gene

This gene has 10 transcripts (splice variants), 209 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000070001.2	ARHGAP10-207	3361	872aa	ENSBTAP00000060334.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LTD9	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 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,
ENSBTAT00000081356.2	ARHGAP10-206	3448	801aa	ENSBTAP00000067414.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MA05	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,
ENSBTAT00000107341.1	ARHGAP10-208	3365	740aa	ENSBTAP00000093342.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSBTAT00000067125.2	ARHGAP10-204	3106	761aa	ENSBTAP00000074425.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1MRK0	-
ENSBTAT00000069953.2	ARHGAP10-201	3098	844aa	ENSBTAP00000058404.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LNK6	-
ENSBTAT00000079235.2	ARHGAP10-205	3088	755aa	ENSBTAP00000059930.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1LWT6	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,
ENSBTAT00000069013.2	ARHGAP10-209	3071	810aa	ENSBTAP00000064642.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1N4C7	-
ENSBTAT00000003283.7	ARHGAP10-202	3071	753aa	ENSBTAP00000003283.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q08DP6	-
ENSBTAT00000083359.2	ARHGAP10-203	3067	748aa	ENSBTAP00000063887.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A3Q1M6F6	-
ENSBTAT00000097523.1	ARHGAP10-210	3019	724aa	ENSBTAP00000083793.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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