Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: hsh2d ENSDARG00000042908

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Description

hematopoietic SH2 domain containing [Source:NCBI gene (formerly Entrezgene);Acc:548337]

Gene Synonyms

wu:fk78a10, zgc:113273

Location

Chromosome 22: 15,570,965-15,578,402 reverse strand.

GRCz11:CM002906.2

About this gene

This gene has 2 transcripts (splice variants), 159 orthologues and 7 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000062986.4	hsh2d-201	2184	365aa	ENSDARP00000062985.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QBJ1	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,
ENSDART00000176291.2	hsh2d-202	2246	365aa	ENSDARP00000143536.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1QBJ1	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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