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
External references
Supporting evidence
ID History
- Gene history

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Gene: Sh2d7 ENSRNOG00000023870

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Description

SH2 domain containing 7 [Source:RGD Symbol;Acc:1309791]

Gene Synonyms

LOC300718, RGD1309791

Location

Primary_assembly 8: 63,814,553-63,826,632 forward strand.

GRCr8:CM070398.1

About this gene

This gene has 2 transcripts (splice variants), 219 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000109765.2	Sh2d7-202	3164	459aa	ENSRNOP00000081811.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5ZSU9	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,
ENSRNOT00000104144.2	Sh2d7-201	3056	429aa	ENSRNOP00000082298.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6G9A7	-

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Summary

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