Homo sapiens Gene: GSG2
Summary
InnateDB Gene IDBG-17889.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GSG2
Gene Name germ cell associated 2 (haspin)
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000177602
Encoded Proteins
germ cell associated 2 (haspin)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 17:3723903-3726699
Strand Forward strand
Band p13.2
Transcripts
ENST00000325418 ENSP00000325290
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 4 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 1 [view]
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0004672 protein kinase activity
GO:0004674 protein serine/threonine kinase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016772 transferase activity, transferring phosphorus-containing groups
GO:0072354 histone kinase activity (H3-T3 specific)
Biological Process
GO:0006468 protein phosphorylation
GO:0007064 mitotic sister chromatid cohesion
GO:0035556 intracellular signal transduction
GO:0071459 protein localization to chromosome, centromeric region
GO:0090231 regulation of spindle checkpoint
GO:2000134 negative regulation of G1/S transition of mitotic cell cycle
GO:2000751 histone H3-T3 phosphorylation involved in chromosome passenger complex localization to kinetochore
Cellular Component
GO:0005634 nucleus
GO:0005694 chromosome
GO:0005737 cytoplasm
GO:0005813 centrosome
GO:0005819 spindle
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt Q8TF76
TrEMBL
UniProt Splice Variant
Entrez Gene 83903
UniGene Hs.534059
RefSeq NM_031965
HUGO HGNC:19682
OMIM 609240
CCDS CCDS11036
HPRD
IMGT
EMBL AB039834 AC116914 AF289865 AK056691 BC047457
GenPept AAH47457 AAK30300 BAB21938 BAB71255
RNA Seq Atlas 83903