HASPIN (histone H3 associated protein kinase)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 83903 |
| Gene name | Histone H3 associated protein kinase |
| Gene symbol | HASPIN |
| Synonyms (NCBI Gene) |
GSG2
|
| Chromosome | 17 |
| Chromosome location | 17p13.2 |
|
miRNA
miRNA information provided by mirtarbase database.
171
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
35
|
|||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Protein
Protein information from UniProt database.
|
|||||||||||
|
UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
|
Q8TF76 | ||||||||||
| Protein name | Serine/threonine-protein kinase haspin (EC 2.7.11.1) (Germ cell-specific gene 2 protein) (H-haspin) (Haploid germ cell-specific nuclear protein kinase) | ||||||||||
| Protein function | Serine/threonine-protein kinase that phosphorylates histone H3 at 'Thr-3' (H3T3ph) during mitosis. May act through H3T3ph to both position and modulate activation of AURKB and other components of the chromosomal passenger complex (CPC) at centro | ||||||||||
| PDB | 2VUW , 2WB8 , 3DLZ , 3E7V , 3F2N , 3FMD , 3IQ7 , 4OUC , 4QTC , 5HTB , 5HTC , 6G34 , 6G35 , 6G36 , 6G37 , 6G38 , 6G39 , 6G3A , 6Z56 , 6Z57 , 6Z58 , 6Z59 , 6Z5A , 6Z5B , 6Z5C , 6Z5D , 6Z5E , 7AVQ , 7OPS , 7SQM , 8RDK , 9B2S , 9B2T , 9B2U , 9FLB , 9FLC , 9FLO , 9FLQ , 9FLR , 9FLT | ||||||||||
| Family and domains |
Pfam
|
||||||||||
| Tissue specificity | TISSUE SPECIFICITY: Strongly expressed in testis. Also present in thymus and bone marrow and low levels observed in prostate, intestine, lung, spleen and lymph node. Expressed in fetal skin, liver, kidney and small intestine and also in proliferating but | ||||||||||
| Sequence |
|
||||||||||
| Sequence length | 798 | ||||||||||
| Interactions | View interactions | ||||||||||
|
Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
|||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||