abnormal cell nucleus count Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absent or greater than one nuclei present per cell body when one is expected; often due to failed cytokinesis or events leading to apoptosis (Mammalian Phenotype Ontology, MP_0003706)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003706
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14 gene mutations causing the abnormal cell nucleus count phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AURKB aurora kinase B
BIRC5 baculoviral IAP repeat containing 5
CDCA8 cell division cycle associated 8
CDK1 cyclin-dependent kinase 1
CTNND1 catenin (cadherin-associated protein), delta 1
DAXX death-domain associated protein
FZR1 fizzy/cell division cycle 20 related 1 (Drosophila)
GLRX3 glutaredoxin 3
LATS2 large tumor suppressor kinase 2
NEK7 NIMA-related kinase 7
NOC3L nucleolar complex associated 3 homolog (S. cerevisiae)
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SPG20 spastic paraplegia 20 (Troyer syndrome)
TTYH1 tweety family member 1