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
External references
Supporting evidence
ID History
- Gene history

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Gene: Shf ENSRNOG00000028685

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Description

Src homology 2 domain containing F [Source:RGD Symbol;Acc:1562705]

Gene Synonyms

LOC108353426, LOC362205, RGD1562705

Location

Primary_assembly 3: 129,749,584-129,769,929 reverse strand.

GRCr8:CM070393.1

About this gene

This gene has 3 transcripts (splice variants), 202 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000064592.5	Shf-201	2464	484aa	ENSRNOP00000059526.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M4K0	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,
ENSRNOT00000111933.2	Shf-203	2398	462aa	ENSRNOP00000082993.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZUK8	-
ENSRNOT00000102854.2	Shf-202	1906	286aa	ENSRNOP00000084391.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZZG0	-

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Summary

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