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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Paralogues
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: GSG2 ENSG00000177602

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Description

germ cell associated 2 (haspin) [Source:HGNC Symbol;Acc:19682]

Gene Synonyms

HASPIN, haspin

Location

Chromosome 17: 3,627,211-3,630,067 forward strand.

GRCh37:CM000679.1

About this gene

This gene has 1 transcript (splice variant).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000325418.4	GSG2-001	2857	798aa	ENSP00000325290.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS11036	Q8TF76	NM_031965.2	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, The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,

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Summary

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