KEGG   VARIANT: 23397v1
Entry
23397v1                      Variant                               
Name
NCAPH mutation
Gene
NCAPH  non-SMC condensin I complex subunit H [KO:K06676]
Organism
hsa_var Human gene variants (Homo sapiens)
Variation
mutations
OmimVar: 602332
Network
nt06512  Chromosome cohesion and segregation
Disease
H00269  Primary microcephaly
Reference
  Authors
Martin CA, Murray JE, Carroll P, Leitch A, Mackenzie KJ, Halachev M, Fetit AE, Keith C, Bicknell LS, Fluteau A, Gautier P, Hall EA, Joss S, Soares G, Silva J, Bober MB, Duker A, Wise CA, Quigley AJ, Phadke SR, Wood AJ, Vagnarelli P, Jackson AP
  Title
Mutations in genes encoding condensin complex proteins cause microcephaly through decatenation failure at mitosis.
  Journal
Genes Dev 30:2158-2172 (2016)
DOI:10.1101/gad.286351.116
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