Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: SH3RF1 ENSPTRG00000016587

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Description

SH3 domain containing ring finger 1 [Source:VGNC Symbol;Acc:VGNC:685]

Location

Chromosome 4: 173,190,542-173,364,278 reverse strand.

Pan_tro_3.0:CM000318.3

About this gene

This gene has 2 transcripts (splice variants), 207 orthologues and 14 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000030825.4	SH3RF1-201	2667	888aa	ENSPTRP00000028466.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A6D2Y8M6 H2QQE8	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,
ENSPTRT00000106831.1	SH3RF1-202	2394	797aa	ENSPTRP00000083719.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3T3B6	-

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Summary

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