90 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Adam10Pied/Adam10+ Hrhr/Hrhr Tg(KRT14-Kitl*)4XTG2Bjl/0 involves: C57BL/6J * HRA/SkhKcl * SJL	abnormal skin pigmentation	J:262499
	hairless	J:262499
Baxtm1Sjk/Bax+ KitlSl/KitlSl Tg(Pou5f1-GFP)1Scho/? involves: 129X1/SvJ * C3H * CD-1 * FVB	abnormal primordial germ cell proliferation	J:115283
Baxtm1Sjk/Baxtm1Sjk KitlSl/KitlSl Tg(Pou5f1-GFP)1Scho/? involves: 129X1/SvJ * C3H * CD-1 * FVB	abnormal primordial germ cell migration	J:115283
	abnormal primordial germ cell proliferation	J:115283
KitlSl-10H/Kitl+ involves: 101/H * C3H/HeH	abnormal foot pigmentation	J:14014
	diluted coat color	J:14014
	head spot	J:14014
	white spotting	J:14014
KitlSl-10H/KitlSl-10H involves: 101/H * C3H/HeH	anemia	J:14014, J:31566
	lethality throughout fetal growth and development, complete penetrance	J:31566
KitlSl-18H/Kitl+ involves: 101/H * C3H/HeH	anemia	J:18280
	belly spot	J:18280
	diluted coat color	J:18280
	head blaze	J:18280
	head spot	J:18280
	hypopigmentation	J:18280
	pallor	J:18280
	postnatal lethality, incomplete penetrance	J:18280
	white spotting	J:18280
KitlSl-18H/Kitl+ X/SryAKR/J involves: AKR/J * C57BL/6J	decreased testis weight	J:133266
KitlSl-18H/KitlSl-18H involves: 101/H * C3H/HeH	embryonic lethality	J:18280
	embryonic lethality between implantation and somite formation	J:18280
KitlSl-18H/KitlSl-con Not Specified	diluted coat color	J:18280
	head blaze	J:18280
KitlSl-d/Kitl+ rs/rs involves: C3H/HeJ * DBA/2J	absent coat pigmentation	J:125080
KitlSl-d/Kitl+ Ph/Ph+ involves: C57BL/Gr * DBA/2J	abnormal coat/hair pigmentation	J:125080
	head spot	J:125080
	irregular coat pigmentation	J:125080
KitlSl-d/KitlSl-d Tg(Mt1-RET)304Ina/0 involves: BALB/c * C57BL/6 * DBA/2	decreased tumor incidence	J:88074
	increased melanoma incidence	J:88074
KitlSl-gb/Kitl+ C3.Cg-KitlSl-gb	abnormal ventral coat pigmentation	J:79293
	head spot	J:79293
	increased mean corpuscular hemoglobin	J:79293
	increased mean corpuscular volume	J:79293
	macrocytic anemia	J:79293
KitlSl-gb/KitlSl-gb C3.Cg-KitlSl-gb	abnormal primordial germ cell migration	J:115437
	abnormal primordial germ cell morphology	J:115437
	abnormal primordial germ cell proliferation	J:115437
	absent primordial germ cells	J:115437
	decreased primordial germ cell number	J:115437
	increased primordial germ cell apoptosis	J:115437
	lethality throughout fetal growth and development, incomplete penetrance	J:79293
	low mean erythrocyte cell number	J:79293
	macrocytic anemia	J:79293
	perinatal lethality, complete penetrance	J:79293
	prenatal lethality, incomplete penetrance	J:79293
KitlSl-J/Kitl+ C3HeB/FeHu-KitlSl-J	belly spot	J:145144
	diluted coat color	J:145144
	white spotting	J:145144
KitlSl-J/Kitl+ involves: 129	increased testicular teratoma incidence	J:50508
KitlSl-J/KitlSl-J C3HeB/FeHu-KitlSl-J	abnormal seminiferous tubule morphology	J:145144
	absent germ cells	J:145144
	absent ovarian follicles	J:145144
	anemia	J:145144
	perinatal lethality, complete penetrance	J:145144
KitlSl-pan/Kitl+ either: (involves: C3H/HeJ * C57BL/6J) or (involves: C3H/HeN * C57BL/6J)	decreased primordial germ cell number	J:23593
	diluted coat color	J:23593
	normal reproductive system phenotype	J:23593
KitlSl-pan/KitlSl-pan either: (involves: C3H/HeJ * C57BL/6J) or (involves: C3H/HeN * C57BL/6J)	decreased oocyte number	J:23593
	decreased primordial germ cell number	J:23593
	female infertility	J:23593
	impaired ovarian folliculogenesis	J:23593
	normal reproductive system phenotype	J:23593
	white spotting	J:23593
KitlSl-pan/KitlSl-pan involves: C3H	decreased male germ cell number	J:4746
	decreased oocyte number	J:4746
	decreased primordial germ cell number	J:4746
	female infertility	J:4746
	impaired ovarian folliculogenesis	J:4746
	irregular coat pigmentation	J:4746
	macrocytic anemia	J:4746
	small ovary	J:4746
	white spotting	J:4746
KitlSl/Kitl+ either: (involves: C3H * WC) or (involves: C3H * C57BL/6 * DBA/2J * WC)	anemia	J:6084
	decreased mast cell number	J:6084
KitlSl/Kitl+ involves: 129/Sv * C3H	increased testicular teratoma incidence	J:50508
	increased tumor incidence	J:50508
KitlSl/Kitl+ involves: C3H	abnormal vibrissa morphology	J:3399
	anemia	J:3399
	belly spot	J:3399, J:157170
	decreased ear pigmentation	J:3399
	decreased erythrocyte cell number	J:3399
	decreased foot pigmentation	J:3399
	diluted coat color	J:3399, J:157170
	head blaze	J:3399
	head spot	J:3399
	pallor	J:3399
	normal reproductive system phenotype	J:3399
KitlSl/Kitl+ Tg(PGK1-KITLG*220)441Daw/0 involves: C3H	abnormal coat/hair pigmentation	J:32600
	decreased mast cell number	J:32600
	hypopigmentation	J:32600
KitlSl/KitlSl-17J involves: BALB/cGr * C3HeB/FeJ	absent coat pigmentation	J:79402
KitlSl/KitlSl-Clo Not Specified	abnormal coat/hair pigmentation	J:13654
	absent coat pigmentation	J:13654
KitlSl/KitlSl-d (WC/ReJ KitlSl x B6.D2-KitlSl-d/J)F1-KitlSl/KitlSl-d/J	abnormal osteoblast physiology	J:111273
	abnormal osteoclast morphology	J:111273
	abnormal skeleton development	J:111273
	decreased body weight	J:111273
	decreased bone mineral content	J:111273
	decreased bone mineral density	J:111273
	decreased compact bone thickness	J:111273
	decreased trabecular bone volume	J:111273
	increased erythrocyte protoporphyrin level	J:5985
	postnatal growth retardation	J:111273
KitlSl/KitlSl-d involves: C3H * C57BL/6 * DBA/2J * WC	abnormal response to transplant	J:6084
	decreased mast cell number	J:6084
KitlSl/KitlSl-d involves: C57BL/6 * WC	abnormal forestomach morphology	J:2777
	abnormal stomach epithelium morphology	J:2777
	abnormal stomach non-glandular epithelium morphology	J:2777
	abnormal tumor incidence	J:5758
	anemia	J:2777, J:27511
	decreased hematocrit	J:27511
	decreased primordial germ cell number	J:5547
	dermatitis	J:5758
	gastric ulcer	J:2777
	increased leukemia incidence	J:5758
	increased papilloma incidence	J:2777
	infertility	J:5547
	premature death	J:5758
	normal reproductive system phenotype	J:5547
	reticulocytosis	J:27511
	stomach inflammation	J:2777
	thymus atrophy	J:5758
	weight loss	J:5758
KitlSl/KitlSl involves: C3H	abnormal blood circulation	J:3399
	abnormal brain development	J:3399
	absent skin pigmentation	J:28098
	anemia	J:3399
	infertility	J:5547
	lethality throughout fetal growth and development, complete penetrance	J:3399
	myelencephalic blebs	J:3399
	pallor	J:3399
	spina bifida	J:3399
Kitltm2.1Pbes/KitlSl involves: 129S1/Sv * C3H * C57BL/6J * FVB/N	azoospermia	J:157170
	diluted coat color	J:157170
Mc1re/Mc1re Tg(KRT14-Kitl)1Takk/0 involves: C57BL/6 * SJL	abnormal melanogenesis	J:112959
Mc1re/Mc1re Xpctm1Brd/Xpctm1Brd Tg(KRT14-Kitl)1Takk/0 involves: 129S7/SvEvBrd * C57BL/6 * SJL	increased squamous cell carcinoma incidence	J:112959
	increased tumor incidence	J:112959
	skin lesions	J:112959
	thick epidermis	J:112959
	weight loss	J:112959
Xpatm1Tnka/Xpatm1Tnka Tg(KRT14-Kitl)1Takk/? involves: C57BL/6 * CBA * SJL	abnormal coat/hair pigmentation	J:100608
	abnormal epidermal pigmentation	J:100608
	increased metastatic potential	J:100608
	increased skin tumor incidence	J:100608