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

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Gene: SH3RF1 ENSSSCG00000009716

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Description

SH3 domain containing ring finger 1 [Source:VGNC Symbol;Acc:VGNC:98316]

Location

Primary_assembly 14: 20,420,618-20,559,271 forward strand.

Sscrofa11.1:CM000825.5

About this gene

This gene has 1 transcript (splice variant), 207 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000010652.5	SH3RF1-201	4251	849aa	ENSSSCP00000010375.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D0ULG9 F1RIX9	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 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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