PRKY: Difference between revisions

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{{PBB_Summary
{{PBB_Summary
| section_title =  
| section_title =  
| summary_text = This gene encodes a member of the cAMP-dependent serine/threonine protein kinase family. This gene is located on chromosome Y, near the boundary of the pseudoautosomal region. Abnormal recombination between this gene and a related gene on chromosome X is a frequent cause of XX males and XY females.<ref name="entrez"/>
| summary_text = This gene encodes a member of the [[Protein kinase A|cAMP-dependent]] [[serine/threonine protein kinase]] family. This gene is located on [[chromosome Y (human)|chromosome Y]], near the boundary of the [[pseudoautosomal region]]. Abnormal [[Genetic recombination|recombination]] between this gene and a related gene on [[chromosome X]] is a frequent cause of [[XX male syndrome|XX males]] and [[XY gonadal dysgenesis|XY females]].<ref name="entrez"/>
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Latest revision as of 08:12, 9 January 2019

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Serine/threonine-protein kinase PRKY is an enzyme that in humans is encoded by the PRKY gene.[1][2]

This gene encodes a member of the cAMP-dependent serine/threonine protein kinase family. This gene is located on chromosome Y, near the boundary of the pseudoautosomal region. Abnormal recombination between this gene and a related gene on chromosome X is a frequent cause of XX males and XY females.[2]

References

  1. Klink A, Schiebel K, Winkelmann M, Rao E, Horsthemke B, Ludecke HJ, Claussen U, Scherer G, Rappold G (Sep 1995). "The human protein kinase gene PKX1 on Xp22.3 displays Xp/Yp homology and is a site of chromosomal instability". Hum Mol Genet. 4 (5): 869–78. doi:10.1093/hmg/4.5.869. PMID 7633447.
  2. 2.0 2.1 "Entrez Gene: PRKY protein kinase, Y-linked".

Further reading