abnormality of chromosome segregation Gene Set
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
|
