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NEK8

From Wikipedia, the free encyclopedia
NEK8
Identifiers
AliasesNEK8, JCK, NEK12A, NPHP9, RHPD2, NIMA related kinase 8
External IDsOMIM: 609799; MGI: 1890646; HomoloGene: 84442; GeneCards: NEK8; OMA:NEK8 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_178170

NM_080849

RefSeq (protein)

NP_835464

NP_543125

Location (UCSC)Chr 17: 28.73 – 28.74 MbChr 11: 78.06 – 78.07 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Serine/threonine-protein kinase Nek8, also known as never in mitosis A-related kinase 8, is an enzyme that in humans is encoded by the NEK8 gene.[5][6]

Function

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Nek8 is a member of the serine/threonine-specific protein kinase family related to NIMA (never in mitosis, gene A) of Aspergillus nidulans. The encoded protein may play a role in cell cycle progression from G2 to M phase.[5]

Clinical significance

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Mutations in the NEK8 gene associated with nephronophthisis.[7][8]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000160602Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000017405Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "Entrez Gene: NIMA (never in mitosis gene a)- related kinase 8".
  6. ^ Otto EA, Trapp ML, Schultheiss UT, Helou J, Quarmby LM, Hildebrandt F (March 2008). "NEK8 mutations affect ciliary and centrosomal localization and may cause nephronophthisis". J. Am. Soc. Nephrol. 19 (3): 587–92. doi:10.1681/ASN.2007040490. PMC 2391043. PMID 18199800.587-92&rft.date=2008-03&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2391043#id-name=PMC&rft_id=info:pmid/18199800&rft_id=info:doi/10.1681/ASN.2007040490&rft.aulast=Otto&rft.aufirst=EA&rft.au=Trapp, ML&rft.au=Schultheiss, UT&rft.au=Helou, J&rft.au=Quarmby, LM&rft.au=Hildebrandt, F&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2391043&rfr_id=info:sid/en.wikipedia.org:NEK8" class="Z3988">
  7. ^ Lancaster MA, Gleeson JG (June 2009). "The primary cilium as a cellular signaling center: lessons from disease". Curr. Opin. Genet. Dev. 19 (3): 220–9. doi:10.1016/j.gde.2009.04.008. PMC 2953615. PMID 19477114.220-9&rft.date=2009-06&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953615#id-name=PMC&rft_id=info:pmid/19477114&rft_id=info:doi/10.1016/j.gde.2009.04.008&rft.aulast=Lancaster&rft.aufirst=MA&rft.au=Gleeson, JG&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2953615&rfr_id=info:sid/en.wikipedia.org:NEK8" class="Z3988">
  8. ^ Zalli, D.; Bayliss, R.; Fry, A. M. (21 November 2011). "The Nek8 protein kinase, mutated in the human cystic kidney disease nephronophthisis, is both activated and degraded during ciliogenesis". Human Molecular Genetics. 21 (5): 1155–1171. doi:10.1093/hmg/ddr544. PMC 3277313. PMID 22106379.1155-1171&rft.date=2011-11-21&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277313#id-name=PMC&rft_id=info:pmid/22106379&rft_id=info:doi/10.1093/hmg/ddr544&rft.aulast=Zalli&rft.aufirst=D.&rft.au=Bayliss, R.&rft.au=Fry, A. M.&rft_id=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3277313&rfr_id=info:sid/en.wikipedia.org:NEK8" class="Z3988">

Further reading

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