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

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Gene: ARHGAP30 ENSSSCG00000006372

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Description

Rho GTPase activating protein 30 [Source:VGNC Symbol;Acc:VGNC:85469]

Location

Primary_assembly 4: 89,375,526-89,394,244 forward strand.

Sscrofa11.1:CM000815.5

About this gene

This gene has 4 transcripts (splice variants), 126 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000043112.3	ARHGAP30-204	4173	1099aa	ENSSSCP00000045618.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A287BSE0 A0A8D1P6T6	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,
ENSSSCT00000006982.5	ARHGAP30-203	3584	922aa	ENSSSCP00000006792.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1P5I4 F1S177	-
ENSSSCT00000099436.1	ARHGAP30-202	2774	884aa	ENSSSCP00000078501.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A4X1VT71 A0A8W4FGY9	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,
ENSSSCT00000102188.1	ARHGAP30-201	1349	101aa	ENSSSCP00000077973.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1G5K7 A0A8W4FI31	-

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Summary

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