STK32B - serine/threonine kinase 32B Gene

Also Known as STK32; STKG6; YANK2; HSA250839

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 55351

About STK32B

This gene has 8 transcripts (splice variants), 146 orthologues and 13 paralogues. Broad expression in kidney (RPKM 2.0), testis (RPKM 1.4) and 14 other tissues.

Summary

This gene encodes a serine-threonine protein kinase. Serine-threonine kinases transfer phosphate molecules to the oxygen atoms of serine and threonine. A genomic deletion affecting this gene has been associated with Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2016]

STK32B Products (3)

mRNA Protein Name
NM_001306082.2 NP_001293011.1 serine/threonine-protein kinase 32B isoform 2
NM_001345969.2 NP_001332898.1 serine/threonine-protein kinase 32B isoform 3
NM_018401.3 NP_060871.1 serine/threonine-protein kinase 32B isoform 1

STK32B Protein Structure

Pkinase

Pkinase: Protein kinase domain (23 - 279)

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

serine/threonine-protein kinase 32B

  • gene for serine/threonine protein kinase

Related Diseases

Diseases Alias
Ellis-Van Creveld Syndrome

  • Chondroectodermal Dysplasia

  • Mesoectodermal Dysplasia

  • EVC

  • Ellis Van Creveld Syndrome

  • Mesodermic Dysplasia

  • Ellis-Van Creveld Dysplasia
Essential Tremor

  • Benign Essential Tremor

  • Familial Tremor

  • Hereditary Essential Tremor

  • Essential Hereditary Tremor

  • Shaky Hand Syndrome

  • Benign Essential Tremor Syndrome

  • Tremor Hereditary Essential

  • Essential Tremor, Susceptibility To

  • Tremor, Hereditary Essential
Hemochromatosis, Type 2a

  • Hemochromatosis Type 2a

  • HFE2A

  • Juvenile Hemochromatosis

  • Hemochromatosis 2a

  • Hefe2

  • Hemochromatosis Type 2

  • Jh
Dysostosis

  • Dysostoses
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS13933 STK32B Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Felis catus STK32B VGNC VGNC:65781
Mus musculus STK32B MGD MGI:1927552
Macaca mulatta STK32B VGNC VGNC:78114
Canis familiaris STK32B VGNC VGNC:46914
Bos taurus STK32B VGNC VGNC:106956
Rattus norvegicus STK32B RGD RGD:1306173
Others STK32B NCBI