DYRK1B

Dual specificity tyrosine-phosphorylation-regulated kinase 1B is an enzyme that in humans is encoded by the DYRK1B gene.^[5][6]

DYRK1B
Identifiers
Aliases	DYRK1B, AOMS3, MIRK, dual specificity tyrosine phosphorylation regulated kinase 1B
External IDs	OMIM: 604556; MGI: 1330302; HomoloGene: 31253; GeneCards: DYRK1B; OMA:DYRK1B - orthologs
Gene location (Human) Chr. Chromosome 19 (human)[1] Band 19q13.2 Start 39,825,350 bp[1] End 39,834,201 bp[1]
Gene location (Mouse) Chr. Chromosome 7 (mouse)[2] Band 7|7 A3 Start 27,878,894 bp[2] End 27,886,719 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in muscle of thigh skeletal muscle tissue right testis left testis gastrocnemius muscle right uterine tube pituitary gland right adrenal gland anterior pituitary right adrenal cortex Top expressed in spermatid muscle of thigh spermatocyte seminiferous tubule neural layer of retina genital tubercle lip superior frontal gyrus skeletal muscle tissue granulocyte More reference expression data BioGPS More reference expression data
Gene ontology Molecular function transferase activity protein kinase activity transcription coactivator activity protein serine/threonine/tyrosine kinase activity protein serine/threonine kinase activity protein tyrosine kinase activity nucleotide binding protein binding ATP binding kinase activity Cellular component nucleus Biological process positive regulation of transcription, DNA-templated protein phosphorylation peptidyl-tyrosine phosphorylation myoblast fusion adipose tissue development phosphorylation protein autophosphorylation Sources:Amigo / QuickGO
Orthologs Species Human Mouse Entrez 9149 13549 Ensembl ENSG00000105204 ENSG00000281320 ENSMUSG00000002409 UniProt Q9Y463 Q9Z188 RefSeq (mRNA) NM_004714 NM_006483 NM_006484 NM_001037957 NM_001271370 NM_010092 RefSeq (protein) NP_004705 NP_006474 NP_006475 NP_004705.1 NP_001033046 NP_001258299 NP_034222 Location (UCSC) Chr 19: 39.83 – 39.83 Mb Chr 7: 27.88 – 27.89 Mb PubMed search [3] [4]
Wikidata
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Function

DYRK1B is a member of the DYRK family of protein kinases. DYRK1B contains a bipartite nuclear localization signal and is found mainly in muscle and testis. The protein is proposed to be involved in the regulation of nuclear functions. Three isoforms of DYRK1B have been identified differing in the presence of two alternatively spliced exons within the catalytic domain.^[6]

Interactions

DYRK1B has been shown to interact with:

• PCBD1^[7] and
• RANBP9.^[8]

Clinical significance

One lone missense mutation in Dyrk1B gene (R102C) was found associated with an autosomal dominant early onset Coronary Artery Disease, juvenile-onset truncal obesity, severe hypertension, and type II diabetes mellitus - seen in subjects from a nomadic group in Iran.^[9]

See also

• DYRK1A
• DYRK2