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
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: SHF ENSCSAG00000010264

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Description

Src homology 2 domain containing F [Source:HGNC Symbol;Acc:HGNC:25116]

Location

Chromosome 26: 38,015,850-38,035,761 forward strand.

ChlSab1.1:CM001967.1

About this gene

This gene has 1 transcript (splice variant), 201 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSCSAT00000008352.1	SHF-201	1418	286aa	ENSCSAP00000006501.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0D9RD12	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,

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Summary

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