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

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Gene: Rgs12 ENSRNOG00000030568

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Description

regulator of G-protein signaling 12 [Source:RGD Symbol;Acc:3564]

Location

Primary_assembly 14: 79,940,565-80,034,859 reverse strand.

GRCr8:CM070404.1

About this gene

This gene has 5 transcripts (splice variants), 145 orthologues, 22 paralogues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000040215.7	Rgs12-201	4903	1457aa	ENSRNOP00000045065.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D4AB55	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 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,
ENSRNOT00000045068.5	Rgs12-202	5457	1387aa	ENSRNOP00000047497.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6IK12 G3V9H1	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,
ENSRNOT00000096126.2	Rgs12-205	5322	1348aa	ENSRNOP00000083247.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GAJ3	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,
ENSRNOT00000081570.3	Rgs12-203	2961	803aa	ENSRNOP00000072476.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K326	-
ENSRNOT00000093959.2	Rgs12-204	2019	499aa	ENSRNOP00000096510.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AQL0	-

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Summary

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