Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
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: Hsh2d ENSRNOG00000023614

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Description

hematopoietic SH2 domain containing [Source:RGD Symbol;Acc:2321939]

Gene Synonyms

LOC100360518, LOC306333

Location

Primary_assembly 16: 17,669,345-17,682,013 reverse strand.

GRCr8:CM070406.1

About this gene

This gene has 1 transcript (splice variant), 158 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000038494.7	Hsh2d-201	2176	335aa	ENSRNOP00000037214.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6K9Q2 D3ZRF7	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,

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Summary

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