Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Cellular component
- 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: Sh2d5 ENSRNOG00000014909

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Description

SH2 domain containing 5 [Source:RGD Symbol;Acc:1305952]

Gene Synonyms

LOC366489, RGD1305952

Location

Primary_assembly 5: 155,750,803-155,763,936 forward strand.

GRCr8:CM070395.1

About this gene

This gene has 2 transcripts (splice variants), 141 orthologues and 8 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000076031.4	Sh2d5-201	3288	485aa	ENSRNOP00000068092.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MJD8	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,
ENSRNOT00000076439.4	Sh2d5-202	3094	429aa	ENSRNOP00000068008.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A096MJ64 A6ITG7	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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