abnormal tumor latency Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the expected time of onset of tumor occurrence (Mammalian Phenotype Ontology, MP_0010307)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010307
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19 gene mutations causing the abnormal tumor latency phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BRCA2 breast cancer 2, early onset
BUB1 BUB1 mitotic checkpoint serine/threonine kinase
CACFD1 calcium channel flower domain containing 1
DCLRE1A DNA cross-link repair 1A
EGR1 early growth response 1
ERCC2 excision repair cross-complementation group 2
FOXO3 forkhead box O3
IFNG interferon, gamma
IL22RA2 interleukin 22 receptor, alpha 2
KLF10 Kruppel-like factor 10
MGAT5 mannosyl (alpha-1,6-)-glycoprotein beta-1,6-N-acetyl-glucosaminyltransferase
MSH2 mutS homolog 2
NBN nibrin
PCSK6 proprotein convertase subtilisin/kexin type 6
PRF1 perforin 1 (pore forming protein)
RASAL2 RAS protein activator like 2
RGPD1 RANBP2-like and GRIP domain containing 1
TP53 tumor protein p53
TREM1 triggering receptor expressed on myeloid cells 1