Centromere protein E

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(Redirected from CENPE)

Template:Short description Template:Cs1 config An Error has occurred retrieving Wikidata item for infobox Centromere-associated protein E is a protein that in humans is encoded by the CENPE gene.[1][2]

Centromere-associated protein E is a kinesin-like motor protein that accumulates in the G2 phase of the cell cycle. Unlike other centromere-associated proteins, it is not present during interphase and first appears at the centromere region of chromosomes during prometaphase. CENPE is proposed to be one of the motors responsible for mammalian chromosome movement and/or spindle elongation.[2]

CENPE is also called Kinesin-7.

Clinical significance

Mutations in CENPE result in autosomal recessive primary microcephaly type 13, which includes skeletal abnormalities and immunodeficiency.[3]

See also

References

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  1. ^ Page Module:Citation/CS1/styles.css has no content.Testa JR, Zhou JY, Bell DW, Yen TJ (Mar 1995). "Chromosomal localization of the genes encoding the kinetochore proteins CENPE and CENPF to human chromosomes 4q24→q25 and 1q32→q41, respectively, by fluorescence in situ hybridization". Genomics. 23 (3): 691–3. doi:10.1006/geno.1994.1558. PMID 7851898.
  2. ^ a b Page Module:Citation/CS1/styles.css has no content."Entrez Gene: CENPE centromere protein E, 312kDa".
  3. ^ Page Module:Citation/CS1/styles.css has no content."OMIM Entry - # 616051 - MICROCEPHALY 13, PRIMARY, AUTOSOMAL RECESSIVE; MCPH13". www.omim.org. Retrieved 2020-01-25.

Further reading

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