Gene: STK32B

Alternate names for this Gene: HSA250839|STK32|STKG6|YANK2

Gene 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.

Gene is located in Chromosome: 4

Location in Chromosome : 4p16.2

Description of this Gene: serine/threonine kinase 32B

Type of Gene: protein-coding

rs78647349 in STK32B gene and Alzheimer's Disease PMID 23535033 2014 Genome-wide association study of the rate of cognitive decline in Alzheimer's disease.

rs62291616 in STK32B gene and Blood Protein Measurement PMID 30072576 2018 Co-regulatory networks of human serum proteins link genetics to disease.

rs7673097 in STK32B gene and Coronary heart disease PMID 21626137 2011 Two-marker association tests yield new disease associations for coronary artery disease and hypertension.

rs10937625 in STK32B gene and Essential Tremor PMID 27797806 2016 Genome-wide association study in essential tremor identifies three new loci.

rs16836697 in STK32B gene and Serum albumin measurement PMID 22286219 2012 Genome-wide association study identifies multiple loci influencing human serum metabolite levels.

PMID 23281178 2013 A genome-wide assessment of variability in human serum metabolism.