increased chromosomal stability Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decrease in the probability that whole chromosomes or pieces of chromosomes are gained or lost during cell division, resulting in an imbalance in the number of chromosomes per cell (aneuploidy) and an reduced rate of loss of heterozygosity (Mammalian Phenotype Ontology, MP_0010095)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010095
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Genes

15 gene mutations causing the increased chromosomal stability phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB6 ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group)
CYP20A1 cytochrome P450, family 20, subfamily A, polypeptide 1
GIT2 G protein-coupled receptor kinase interacting ArfGAP 2
HDAC1 histone deacetylase 1
JMJD1C jumonji domain containing 1C
KLK9 kallikrein-related peptidase 9
MIER1 mesoderm induction early response 1, transcriptional regulator
NBEAL2 neurobeachin-like 2
NCAPH non-SMC condensin I complex, subunit H
PLIN2 perilipin 2
RNF10 ring finger protein 10
SETD5 SET domain containing 5
TBC1D10A TBC1 domain family, member 10A
TERF2IP telomeric repeat binding factor 2, interacting protein
ZNF367 zinc finger protein 367