abnormality of chromosome segregation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of chromosome segregation. (Human Phenotype Ontology, HP_0002916)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002916
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Genes

19 genes associated with the abnormality of chromosome segregation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
CDAN1 codanin 1
CTNND2 catenin (cadherin-associated protein), delta 2
ESCO2 establishment of sister chromatid cohesion N-acetyltransferase 2
FMR1 fragile X mental retardation 1
GJA1 gap junction protein, alpha 1, 43kDa
LBR lamin B receptor
LMNB1 lamin B1
MECP2 methyl CpG binding protein 2
NF1 neurofibromin 1
NKX2-5 NK2 homeobox 5
RAI1 retinoic acid induced 1
RB1 retinoblastoma 1
SEC23B Sec23 homolog B (S. cerevisiae)
SEMA5A sema domain, seven thrombospondin repeats (type 1 and type 1-like), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 5A
SHH sonic hedgehog
TBX1 T-box 1
TBX4 T-box 4
TSC1 tuberous sclerosis 1