Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
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: HSH2D ENSPTRG00000023880

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Description

hematopoietic SH2 domain containing [Source:VGNC Symbol;Acc:VGNC:14552]

Location

Chromosome 19: 17,073,568-17,087,246 forward strand.

Pan_tro_3.0:CM000333.3

About this gene

This gene has 2 transcripts (splice variants), 183 orthologues and 4 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSPTRT00000019628.6	HSH2D-201	1996	352aa	ENSPTRP00000018162.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	H2QFN8	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,
ENSPTRT00000088137.1	HSH2D-202	210	69aa	ENSPTRP00000063586.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A2I3RFW7 A0A6D2Y7A7	-

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Summary

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