Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
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: Parvg ENSRNOG00000052064

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Description

parvin, gamma [Source:RGD Symbol;Acc:1597417]

Gene Synonyms

LOC689069

Location

Primary_assembly 7: 115,456,209-115,475,104 forward strand.

mRatBN7.2:CM026980.1

About this gene

This gene has 2 transcripts (splice variants), 191 orthologues, 2 paralogues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000098278.1	Parvg-202	1420	346aa	ENSRNOP00000087942.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A8Y9	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,
ENSRNOT00000085216.2	Parvg-201	2536	331aa	ENSRNOP00000070638.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZWK2	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. 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 P1,

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Summary

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