1. Gene
  2. TSSK2 - testis specific serine kinase 2 Gene

TSSK2 - testis specific serine kinase 2 Gene

Homo sapiens

Also known as TSK2; DGS-G; SPOGA2; STK22B

Gene ID: 23617 | Gene type: protein coding

About TSSK2

Cytogenetic location: 22q11.21 Genomic coordinates (GRCh38): 22:19,131,308-19,132,622 (from NCBI)

This gene has 1 transcript (splice variant), 177 orthologues and 17 paralogues.

Summary

TSSK2 belongs to a family of serine/threonine kinases highly expressed in testis (Hao et al., 2004 [PubMed 15044604]).[supplied by OMIM, Mar 2008]

TSSK2 Products(1)

mRNA Protein Name
NM_053006.5 NP_443732.3 testis-specific serine/threonine-protein kinase 2
Gene Ontology
  • Molecular Function
  • Biological Process
Molecular Function GO Annotation Evidence Reference Source
enables magnesium ion binding IDA
IDA: Inferred from direct assay
20729278 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
15044604 GOA
enables protein serine/threonine kinase activity IDA
IDA: Inferred from direct assay
18533145 GOA
Biological Process GO Annotation Evidence Reference Source
involved in protein autophosphorylation IDA
IDA: Inferred from direct assay
20729278 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TSSK2 Protein Structure

Pkinase

Pkinase: Protein kinase domain (17 - 272)

  • 0
  • 100
  • 200
  • 300
  • 358 a.a.
Protein Preferred Names Protein Names

testis-specific serine/threonine-protein kinase 2

TSK-2

TSSK2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
TSSK2 Q96PF2 FAM229B Homo sapiens Q4G0N7
Y2H Prey Pooling
32296183
Intra
TSSK2 Q96PF2 FAM229B Homo sapiens Q4G0N7
Y2H Array
32296183
Intra
TSSK2 Q96PF2 HSP90AB1 Homo sapiens P08238
Lumier
22939624
Intra
TSSK2 Q96PF2 HSP90AB1 Homo sapiens P08238
Pull Down
32707033
Intra
TSSK2 Q96PF2 TSEN15 Homo sapiens Q8WW01
Y2H Array
32296183
Intra
TSSK2 Q96PF2 TSEN15 Homo sapiens Q8WW01
Y2H Prey Pooling
32296183
Intra
TSSK2 Q96PF2 LZTS2 Homo sapiens Q9BRK4
Y2H Prey Pooling
32296183
Intra
TSSK2 Q96PF2 LZTS2 Homo sapiens Q9BRK4
Y2H Array
32296183
Intra
TSSK2 Q96PF2 LZTS2 Homo sapiens Q9BRK4
Validated Y2H
32296183
Intra
TSSK2 Q96PF2 TSKS Homo sapiens Q9UJT2
Y2H Prey Pooling
32296183
Intra
TSSK2 Q96PF2 TSKS Homo sapiens Q9UJT2
Pull Down
15044604
Intra
TSSK2 Q96PF2 TSKS Homo sapiens Q9UJT2
Y2H Array
32296183
Intra
TSSK2 Q96PF2 TSKS Homo sapiens Q9UJT2
Validated Y2H
32296183
Intra
TSSK2 Q96PF2 TSKS Homo sapiens Q9UJT2-2
Protein Kinase Assay
15044604
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Hyperprolinemia, Type I

Proline Oxidase Deficiency

Hyperprolinemia Type 1

HYRPRO1

Hpi

Hyperprolinemia Type I

Hyperprolinemia 1

Proline Dehydrogenase Deficiency

Digeorge Syndrome

Chromosome 22q11.2 Deletion Syndrome

DGS

Hypoplasia Of Thymus And Parathyroids

Third And Fourth Pharyngeal Pouch Syndrome

22q11.2 Deletion Syndrome

Digeorge Sequence

Digeorge'S Syndrome

Pharyngeal Pouch Syndrome

Di-George Syndrome

Shprintzen Syndrome

Van Den Ende-Gupta Syndrome

VDEGS

Blepharophimosis, Arachnodactyly, And Congenital Contractures

Marden-Walker-Like Syndrome

Marden-Walker-Like Syndrome Without Psychomotor Retardation

Marden Walker Like Syndrome

Marden-Walker-Like Syndrome Without Psychmotor Retardation

Van Den Ende Gupta Syndrome

Marden Walker Like Syndrome Without Psychomotor Retardation

Blepharophimosis Arachnodactyly And Congenital Contractures

Combined D-2- And L-2-Hydroxyglutaric Aciduria

D,L-2-Hydroxyglutaric Aciduria

D2L2AD

Combined D-2-Hydroxyglutaric Acidemia And L-2-Hydroxyglutaric Acidemia

Combined D-2-Hydroxyglutaric Aciduria And L-2-Hydroxyglutaric Aciduria

D,L-2-Hga

D,L-2-Hydroxyglutaric Acidemia

Combined D,L-2-Hydroxyglutaric Aciduria

Spermatogenic Failure

Azoospermia

Spgf

Spermatogenic Failure, Susceptibility To

Absent Sperm

Aspermatogenesis

Infertility Due To Azoospermia

Hypospermatogenesis

Azoospermatism

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta TSSK2 VGNC VGNC:78557
Mus musculus TSSK2 MGD MGI:1347559
Felis catus TSSK2 VGNC VGNC:66644
Rattus norvegicus TSSK2 RGD RGD:1304951
Canis familiaris TSSK2 VGNC VGNC:103714
Bos taurus TSSK2 VGNC VGNC:49975
Others TSSK2 NCBI