PRKY

From Wikipedia, the free encyclopedia


Protein kinase, Y-linked
Identifiers
Symbol(s) PRKY;
External IDs OMIM: 400008
Orthologs
Human Mouse
Entrez 5616 n/a
Ensembl ENSG00000099725 n/a
Uniprot O43930 n/a
Refseq NM_002760 (mRNA)
NP_002751 (protein)
n/a (mRNA)
n/a (protein)
Location Chr Y: 7.2 - 7.31 Mb n/a
Pubmed search [1] n/a

Protein kinase, Y-linked, also known as PRKY, is a human gene.[1]

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.[1]

[edit] References

[edit] Further reading

  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121-7. doi:10.1101/gr.2596504. PMID 15489334. 
  • Skaletsky H, Kuroda-Kawaguchi T, Minx PJ, et al. (2003). "The male-specific region of the human Y chromosome is a mosaic of discrete sequence classes.". Nature 423 (6942): 825-37. doi:10.1038/nature01722. PMID 12815422. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899-903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Jobling MA, Williams GA, Schiebel GA, et al. (1999). "A selective difference between human Y-chromosomal DNA haplotypes.". Curr. Biol. 8 (25): 1391-4. PMID 9889101. 
  • Schiebel K, Winkelmann M, Mertz A, et al. (1998). "Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females.". Hum. Mol. Genet. 6 (11): 1985-9. PMID 9302280. 
  • Schiebel K, Mertz A, Winkelmann M, et al. (1997). "FISH localization of the human Y-homolog of protein kinase PRKX (PRKY) to Yp11.2 and two pseudogenes to 15q26 and Xq12-->q13.". Cytogenet. Cell Genet. 76 (1-2): 49-52. PMID 9154127. 
  • Gläser B, Hierl T, Taylor K, et al. (1997). "High-resolution fluorescence in situ hybridization of human Y-linked genes on released chromatin.". Chromosome Res. 5 (1): 23-30. PMID 9088640. 
  • Klink A, Schiebel K, Winkelmann M, et al. (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. PMID 7633447.