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Symbol
Name
ID

Fancc
Fanconi anemia, complementation group C
MGI:95480

Phenotype annotations related to cellular

Darker colors indicate more annotations

Human Phenotypes	Abnormality of chromosome stability	Chromosomal breakage induced by crosslinking agents	Deficient excision of UV-induced pyrimidine dimers in DNA	Prolonged G2 phase of cell cycle
Disease(s) Associated with FANCC	Abnormality of chromosome stability	Chromosomal breakage induced by crosslinking agents	Deficient excision of UV-induced pyrimidine dimers in DNA	Prolonged G2 phase of cell cycle
Fanconi anemia
Fanconi anemia complementation group C

Mouse Phenotypes		decreased oocyte number	oligozoospermia	decreased germ cell number	decreased telomere length	abnormal cell cycle checkpoint function	increased cellular sensitivity to methylmethanesulfonate	induced chromosome breakage	spontaneous chromosome breakage
Availability	Mouse Genotype	decreased oocyte number	oligozoospermia	decreased germ cell number	decreased telomere length	abnormal cell cycle checkpoint function	increased cellular sensitivity to methylmethanesulfonate	induced chromosome breakage	spontaneous chromosome breakage
	Fancc^tm1Mab/Fancc^tm1Mab
	Fancc^tm1Mgo/Fancc^tm1Mgo

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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