CENPT

Centromere- and microtubule-associated protein From Wikipedia, the free encyclopedia

Centromere protein T is a protein that in humans is encoded by the CENPT gene.[5][6][7]

AliasesCENPT, C16orf56, CENP-T, centromere protein T, SSMGA
End67,847,811 bp[1]
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CENPT
Identifiers
AliasesCENPT, C16orf56, CENP-T, centromere protein T, SSMGA
External IDsOMIM: 611510; MGI: 2443939; HomoloGene: 41610; GeneCards: CENPT; OMA:CENPT - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_025082

NM_177150

RefSeq (protein)

NP_079358

NP_796124

Location (UCSC)Chr 16: 67.83 – 67.85 MbChr 8: 106.57 – 106.58 Mb
PubMed search[3][4]
Wikidata
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Clinical significance

Mutations in CENPT cause an autosomal recessive syndrome of microcephaly, short stature, skeletal abnormalities, underdeveloped genitalia and pubertal delay.[8]

See also

References

Further reading

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