34 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Fancctm1Mab/Fancctm1Mab involves: 129S1/Sv * 129X1/SvJ * C57BL/6	decreased telomere length	J:157096
Fancctm1Mab/Fancctm1Mab involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	abnormal common lymphocyte progenitor cell morphology	J:71134
	abnormal fertility/fecundity	J:32080
	abnormal hematopoietic stem cell physiology	J:47897
	abnormal hematopoietic system physiology	J:47897
	abnormal ovary morphology	J:32080
	abnormal reproductive system morphology	J:32080
	absent corpus luteum	J:32080
	arrest of spermatogenesis	J:32080
	decreased common myeloid progenitor cell number	J:71134
	decreased litter size	J:32080
	female infertility	J:32080
	normal hematopoietic system phenotype	J:32080
	impaired ovarian folliculogenesis	J:32080
	increased cellular sensitivity to methylmethanesulfonate	J:47897
	male infertility	J:32080
	reduced fertility	J:32080
	seminiferous tubule degeneration	J:32080
	testicular atrophy	J:32080
	thrombocytopenia	J:71134
Fancctm1Mgo/Fancctm1Mgo involves: 129S4/SvJaeSor * C57BL/6	abnormal cell cycle checkpoint function	J:61512
	abnormal seminiferous tubule morphology	J:61512
	absent common myeloid progenitor cells	J:61512
	absent ovarian follicles	J:61512
	decreased germ cell number	J:61512
	decreased litter size	J:61512
	decreased oocyte number	J:61512
	decreased testis weight	J:61512
	induced chromosome breakage	J:61512
	oligozoospermia	J:61512
	ovary hypoplasia	J:61512
	reduced female fertility	J:61512
	small ovary	J:61512
	spontaneous chromosome breakage	J:61512
	uterus hypoplasia	J:61512