242 phenotypes from 90 alleles in 90 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kitd18/Kit+ involves: 129P2/OlaHsd * C57BL/6	belly spot	J:97533
KitM1Hmgu/Kit+ C3HeB/FeJ-KitM1Hmgu	decreased mean corpuscular hemoglobin	J:186868
	decreased mean corpuscular volume	J:186868
	increased erythrocyte cell number	J:186868
	increased hematocrit	J:186868
KitMhdasco1/Kit+ C3HeB/FeJ-KitMhdasco1	abnormal coat/hair pigmentation	J:86685
KitMhdasco1/KitMhdasco1 C3HeB/FeJ-KitMhdasco1	abnormal coat/hair pigmentation	J:125831
	abnormal erythrocyte morphology	J:125831
	decreased erythrocyte cell number	J:125831
	decreased hematocrit	J:125831
	increased hemoglobin content	J:125831
	increased mean corpuscular volume	J:125831
	macrocytic anemia	J:125831
	normal reproductive system phenotype	J:125831
KitMhdasco5/Kit+ C3HeB/FeJ-KitMhdasco5	abnormal coat/hair pigmentation	J:86685
KitMhdasco5/KitMhdasco5 C3HeB/FeJ-KitMhdasco5	abnormal coat/hair pigmentation	J:125831
	abnormal erythrocyte morphology	J:125831
	decreased circulating cholesterol level	J:125831
	decreased circulating HDL cholesterol level	J:125831
	decreased circulating LDL cholesterol level	J:125831
	decreased erythrocyte cell number	J:125831
	decreased hematocrit	J:125831
	hepatic steatosis	J:125831
	increased hemoglobin content	J:125831
	increased mean corpuscular volume	J:125831
	macrocytic anemia	J:125831
	postnatal lethality, incomplete penetrance	J:125831
	normal reproductive system phenotype	J:125831
	slow postnatal weight gain	J:125831
KitMhdasow3/Kit+ C3HeB/FeJ-KitMhdasow3	belly spot	J:86685
	head blaze	J:86685
KitMhdasow3/KitMhdasow3 C3HeB/FeJ-KitMhdasow3	abnormal coat/hair pigmentation	J:125831
	abnormal spermatogenesis	J:125831
	male infertility	J:125831
KitSsm/Kit+ involves: C57BL/10 * Non-inbred	male infertility	J:14020
	variable body spotting	J:14020
KitSsm/KitSsm involves: C57BL/10 * Non-inbred	anemia	J:14020
	neonatal lethality, complete penetrance	J:14020
Kittm1.1(cre)Jmol/Kittm2.1(cre/Esr1*)Jmol involves: 129/Sv * 129S4/SvJaeSor * C57BL/6J	neonatal lethality, complete penetrance	J:210584
Kittm1.1Bsm/Kittm1.1Bsm B6.129S1-Kittm1.1Bsm	arrest of spermatogenesis	J:90485
	normal hematopoietic system phenotype	J:90485
	normal immune system phenotype	J:90485
	normal pigmentation phenotype	J:90485
Kittm1.1Bsm/Kittm1.1Bsm involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N	abnormal mast cell physiology	J:61141
	abnormal ovary morphology	J:61141
	arrest of spermatogenesis	J:61141
	decreased male germ cell number	J:61141
	decreased mast cell number	J:61141
	decreased secondary ovarian follicle number	J:61141
	decreased tertiary ovarian follicle number	J:61141
	normal hematopoietic system phenotype	J:61141
	impaired ovarian folliculogenesis	J:61141
	increased circulating luteinizing hormone level	J:61141
	increased Leydig cell number	J:61141
	male infertility	J:61141
	ovary cyst	J:61141
	ovary hyperplasia	J:61141
	normal pigmentation phenotype	J:61141
	reduced female fertility	J:61141
	normal reproductive system phenotype	J:61141
Kittm1.1Bsm/Kittm1.1Bsm involves: 129S1/Sv * C57BL/6J	normal homeostasis/metabolism phenotype	J:146561
Kittm1.1Bsm/KitW involves: 129S1/Sv * C57BL/6	abnormal ventral coat pigmentation	J:90485
Kittm1.1Gnf/Kittm1.1Gnf NOD.Cg-Kittm1.1Gnf	normal homeostasis/metabolism phenotype	J:211930
Kittm1Alf/Kit+ involves: 129S2/SvPas	abnormal female reproductive system morphology	J:67923
	abnormal male germ cell morphology	J:103157
	abnormal male reproductive system morphology	J:103157
	abnormal melanoblast migration	J:36230
	abnormal oocyte morphology	J:67923
	abnormal ovarian follicle number	J:67923
	abnormal ovarian folliculogenesis	J:67923
	asthenozoospermia	J:103157
	decreased epididymis weight	J:103157
	decreased primordial ovarian follicle number	J:67923
	decreased testis weight	J:103157
	non-pigmented tail tip	J:36230
	oligozoospermia	J:103157
	reduced male fertility	J:103157
	white spotting	J:36230
Kittm1Alf/KitMhdasow3 involves: 129S2/SvPas * C3HeB/FeJ	abnormal spermatogenesis	J:125831
	hepatic steatosis	J:125831
Kittm1Alf/Kittm1Alf involves: 129S2/SvPas	abnormal female germ cell morphology	J:36230
	abnormal melanoblast migration	J:36230
	abnormal melanocyte morphology	J:36230
	abnormal primordial germ cell migration	J:36230
	anemia	J:103157
	macrocytic anemia	J:36230
	neonatal lethality, complete penetrance	J:36230, J:103157
	pallor	J:36230
Kittm1Ber/Kit+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal coat/hair pigmentation	J:89602
	absent coat pigmentation	J:89602
	normal reproductive system phenotype	J:89602
	variable depigmentation	J:89602
	white spotting	J:89602
Kittm1Ber/Kittm1Ber involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal coat/hair pigmentation	J:89602
	absent coat pigmentation	J:89602
	decreased mast cell number	J:89602
	normal digestive/alimentary phenotype	J:89602
	normal immune system phenotype	J:89602
	normal reproductive system phenotype	J:89602
	variable depigmentation	J:89602
	white spotting	J:89602
Kittm1Bpr/Kit+ either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	abnormal digestive system morphology	J:100778
	increased gastrointestinal stromal tumor incidence	J:100778
	normal pigmentation phenotype	J:100778
Kittm1Bpr/Kittm1Bpr either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6)	abnormal cecum morphology	J:100778
	abnormal digestive system morphology	J:100778
	abnormal ovary morphology	J:100778
	abnormal seminiferous tubule morphology	J:100778
	absent coat pigmentation	J:100778
	absent oocytes	J:100778
	azoospermia	J:100778
	decreased mast cell number	J:100778
	decreased tumor-free survival time	J:100778
	distended abdomen	J:100778
	distended ileum	J:100778
	female infertility	J:100778
	increased gastrointestinal stromal tumor incidence	J:100778
	increased Leydig cell number	J:100778
	intestinal obstruction	J:100778
	male infertility	J:100778
	small ovary	J:100778
Kittm1Bsm/Kit+ involves: 129S1/Sv * C57BL/6J	abnormal foot pigmentation	J:61141
	belly spot	J:61141
	non-pigmented tail tip	J:61141
Kittm1Bsm/Kittm1Bsm involves: 129S1/Sv * C57BL/6J	absent coat pigmentation	J:61141
	decreased mast cell number	J:61141
	infertility	J:61141
	normal pigmentation phenotype	J:61141
Kittm1Hntr/Kittm1Hntr either: (involves: 129/Sv * C57BL/6 * DBA/2) or (involves: 129S1)	abnormal seminiferous tubule morphology	J:60192
	abnormal spermatogonia proliferation	J:60192
	arrest of spermatogenesis	J:60192
	normal growth/size/body region phenotype	J:60192
	normal hematopoietic system phenotype	J:60192
	male infertility	J:60192
	normal pigmentation phenotype	J:60192
	testis hypoplasia	J:60192
Kittm1Rosay/Kit+ involves: 129S7/SvEvBrd * C57BL/6J	belly spot	J:168676
	white spotting	J:168676
Kittm1Rosay/Kittm1Rosay involves: 129S7/SvEvBrd * C57BL/6J	embryonic lethality, complete penetrance	J:168676
Kittm1Shta/Kit+ involves: 129S6/SvEvTac * C57BL/6 * FVB/N	abnormal digestive system morphology	J:130890
	abnormal esophagus morphology	J:130890
	increased gastrointestinal stromal tumor incidence	J:130890
	normal reproductive system phenotype	J:130890
Kittm1Shta/Kittm1Shta involves: 129S6/SvEvTac * C57BL/6 * FVB/N	abnormal digestive system morphology	J:130890
	abnormal esophagus morphology	J:130890
	distended ileum	J:130890
	distended stomach	J:130890
	increased gastrointestinal stromal tumor incidence	J:130890
	premature death	J:130890
	normal reproductive system phenotype	J:130890
Kittm2Ber/Kit+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6	absent coat pigmentation	J:89602
	neonatal lethality, incomplete penetrance	J:89602
	normal reproductive system phenotype	J:89602
	variable depigmentation	J:89602
	white spotting	J:89602
Kittm2Ber/Kittm2Ber involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal coat/hair pigmentation	J:89602
	absent coat pigmentation	J:89602
	decreased mast cell number	J:89602
	normal digestive/alimentary phenotype	J:89602
	normal immune system phenotype	J:89602
	neonatal lethality, incomplete penetrance	J:89602
	normal reproductive system phenotype	J:89602
	variable depigmentation	J:89602
	white spotting	J:89602
Kittm2Ber/Kittm3.1Bsm involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	abnormal erythroid progenitor cell morphology	J:146561
	abnormal proerythroblast morphology	J:146561
Kittm2Bsm/Kit+ involves: 129X1/SvJ * C57BL/6J	abnormal cecum morphology	J:83616
	abnormal esophagus morphology	J:83616
	abnormal myenteric nerve plexus morphology	J:83616
	distended cecum	J:83616
	distended ileum	J:83616
	enlarged cecum	J:83616
	hyperpigmentation	J:83616
	increased gastrointestinal stromal tumor incidence	J:83616
	increased mast cell degranulation	J:83616
	increased mast cell number	J:83616
	interstitial cells of Cajal hyperplasia	J:83616
	premature death	J:83616
	reduced fertility	J:83616
Kittm3.1Bsm/Kittm3.1Bsm B6.129S1-Kittm3.1Bsm	abnormal proerythroblast morphology	J:146561
	abnormal response/metabolism to endogenous compounds	J:146561
	abnormal stress erythropoiesis	J:146561
	decreased erythrocyte cell number	J:146561
	decreased hematocrit	J:146561
	increased erythroblast number	J:146561
	increased mean corpuscular volume	J:146561
	increased physiological sensitivity to xenobiotic	J:146561
	increased susceptibility to xenobiotic induced morbidity/mortality	J:146561
	spleen hypoplasia	J:146561
Kittm3.1Bsm/Kittm3.1Bsm involves: 129S1/Sv * C57BL/6	abnormal B cell differentiation	J:90485
	abnormal mast cell physiology	J:90485
	abnormal T cell differentiation	J:90485
	abnormal ventral coat pigmentation	J:90485
	decreased B cell number	J:90485
	decreased mast cell number	J:90485
	normal hematopoietic system phenotype	J:90485
	normal immune system phenotype	J:90485
	normal reproductive system phenotype	J:90485
Kittm3.1Bsm/KitW involves: 129S1/Sv * C57BL/6	abnormal ventral coat pigmentation	J:90485
Kittm3Ber/Kittm3Ber involves: 129S1/Sv * 129X1/SvJ * C57BL/6	abnormal coat/hair pigmentation	J:89602
	absent coat pigmentation	J:89602
	arrested B cell differentiation	J:89602
	decreased mast cell number	J:89602
	normal digestive/alimentary phenotype	J:89602
	enlarged spleen	J:89602
	increased B cell number	J:89602
	increased megakaryocyte cell number	J:89602
	lethality at weaning, incomplete penetrance	J:89602
	meteorism	J:89602
	premature death	J:89602
	normal reproductive system phenotype	J:89602
	spleen hyperplasia	J:89602
	variable depigmentation	J:89602
	white spotting	J:89602
Kittm4.1Bsm/Kit+ involves: 129S1/Sv * C57BL/6J * FVB/N	abnormal erythrocyte morphology	J:188434
	alopecia	J:188434
	decreased mean corpuscular volume	J:188434
	decreased physiological sensitivity to xenobiotic	J:188434
	decreased tumor growth/size	J:188434
	enlarged spleen	J:188434
	increased erythrocyte cell number	J:188434
	increased erythroid progenitor cell number	J:188434
	increased gastrointestinal tumor incidence	J:188434
	increased hematocrit	J:188434
	increased mast cell number	J:188434
	increased mean platelet volume	J:188434
	interstitial cells of Cajal hyperplasia	J:188434
	polycythemia	J:188434
	premature death	J:188434
	reddish skin	J:188434
	small cecum	J:188434
	spleen hyperplasia	J:188434
Kittm5.1Bsm/Kit+ involves: 129S1/Sv * C57BL/6J * FVB/N	decreased mean corpuscular volume	J:188434
	increased gastrointestinal tumor incidence	J:188434
	increased tumor growth/size	J:188434
	interstitial cells of Cajal hyperplasia	J:188434
	lethality, incomplete penetrance	J:188434
	premature death	J:188434
KitW-1Bao/Kit+ C57BL/6J-KitW-1Bao	male infertility	J:88137
	reduced male fertility	J:88137
	variable body spotting	J:88137
	variable depigmentation	J:88137
KitW-1Bao/KitW-1Bao C57BL/6J-KitW-1Bao	embryonic lethality during organogenesis, complete penetrance	J:88137
KitW-2Bao/Kit+ C57BL/6J-KitW-2Bao	variable body spotting	J:88137
KitW-2Bao/Kit+ involves: C57BL/6J	abnormal seminiferous tubule morphology	J:163026
KitW-2Bao/KitW-2Bao C57BL/6J-KitW-2Bao	absent coat pigmentation	J:88137
KitW-2Btlr/Kit+ C57BL/6J-KitW-2Btlr	belly spot	J:133613
	decreased ear pigmentation	J:133613
	decreased tail pigmentation	J:133613
	diluted coat color	J:133613
	variable body spotting	J:133613
KitW-2Btlr/Kit+ involves: C3H/HeN * C57BL/6	head blaze	J:133613
	white spotting	J:133613
KitW-2Btlr/KitW-2Btlr C57BL/6J-KitW-2Btlr	absent coat pigmentation	J:133613
	normal pigmentation phenotype	J:133613
KitW-3Bao/Kit+ C57BL/6J-KitW-3Bao	variable body spotting	J:88137
KitW-3Bao/Kit+ involves: C57BL/6J	abnormal seminiferous tubule morphology	J:163026
	belly spot	J:163026
	normal hematopoietic system phenotype	J:163026
	white spotting	J:163026
KitW-3Bao/KitW-3Bao C57BL/6J-KitW-3Bao	absent coat pigmentation	J:88137
KitW-3Bao/KitW-3Bao involves: C57BL/6J	abnormal male reproductive system physiology	J:163026
	abnormal primordial ovarian follicle morphology	J:163026
	abnormal seminiferous tubule morphology	J:163026
	decreased erythrocyte cell number	J:163026
	decreased fetal size	J:163026
	decreased hematocrit	J:163026
	decreased hemoglobin content	J:163026
	increased mean corpuscular hemoglobin	J:163026
	increased mean corpuscular hemoglobin concentration	J:163026
	macrocytic anemia	J:163026
	macrocytosis	J:163026
	pallor	J:163026
	postnatal lethality	J:163026
KitW-3Btlr/KitW-3Btlr C57BL/6J-KitW-3Btlr	variable body spotting	J:274823
KitW-4Bao/KitW-4Bao involves: C57BL/6J	absent coat pigmentation	J:183004
KitW-17J/Kit+ Not Specified	white spotting	J:78381
KitW-18J/Kit+ involves: C3HeB/Fe * C57BL/6	white spotting	J:101977
KitW-20J/Kit+ C57BL/6J-KitW-20J/J	white spotting	J:6571
KitW-24J/Kit+ Not Specified	white spotting	J:78381
KitW-25J/KitW-25J involves: A/J * C57BL/6J	microcytic anemia	J:64109
KitW-27H/KitW-27H CBA/H-KitW-27H	anemia	J:13934
	belted	J:13934
	postnatal lethality, complete penetrance	J:13934
KitW-28H/Kit+ involves: 101/H * C3H/HeH	white spotting	J:18375
KitW-28H/KitW-28H involves: 101/H * C3H/HeH	anemia	J:18375
	pallor	J:18375
	postnatal lethality, complete penetrance	J:18375
KitW-29H/Kit+ involves: 101/H * C3H/HeH	diluted coat color	J:18375
	white spotting	J:18375
KitW-29H/KitW-29H involves: 101/H * C3H/HeH	absent coat pigmentation	J:18375
KitW-31H/Kit+ Not Specified	abnormal coat/hair pigmentation	J:180729
	absent skin pigmentation	J:180729
	belly spot	J:180729
	head spot	J:180729
KitW-31H/KitW-31H Not Specified	absent coat pigmentation	J:180729
KitW-32H/Kit+ Not Specified	abnormal coat/hair pigmentation	J:180729
	absent skin pigmentation	J:180729
	belly spot	J:180729
	head spot	J:180729
KitW-32H/KitW-32H Not Specified	absent coat pigmentation	J:180729
KitW-34J/Kit+ C57BL/6J-KitW-34J/J	polycythemia	J:6571
KitW-34J/KitW-34J C57BL/6J-KitW-34J/J	perinatal lethality, complete penetrance	J:6571
	prenatal lethality, incomplete penetrance	J:6571
KitW-34J/KitW-39J involves: C57BL/6J	abnormal ovarian follicle number	J:6571
	abnormal spermatogenesis	J:6571
	absent coat pigmentation	J:6571
	infertility	J:6571
	prenatal lethality, incomplete penetrance	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-35J/Kit+ C57BL/6J-KitW-35J/J	polycythemia	J:6571
	small testis	J:6571
KitW-35J/KitW-35J C57BL/6J-KitW-35J/J	perinatal lethality, complete penetrance	J:6571
	prenatal lethality, incomplete penetrance	J:6571
KitW-36H/KitW-36H involves: 101/H * C3H/HeH	anemia	J:20782
	neonatal lethality, incomplete penetrance	J:20782
	prenatal lethality, incomplete penetrance	J:20782
	white spotting	J:20782
KitW-36J/KitW-36J involves: C57BL/6J	perinatal lethality, complete penetrance	J:6571
	prenatal lethality, incomplete penetrance	J:6571
KitW-37J/Kit+ C57BL/6J-KitW-37J/J	irregular coat pigmentation	J:6571
	polycythemia	J:6571
	white spotting	J:6571
KitW-37J/Kit+ involves: C57BL/6 * C57BL/6J	decreased mast cell number	J:27513
	diluted coat color	J:27513
	white spotting	J:27513
KitW-37J/KitW-37J C57BL/6J-KitW-37J/J	perinatal lethality, complete penetrance	J:6571
	prenatal lethality, incomplete penetrance	J:6571
KitW-37J/KitW-39J involves: C57BL/6J	abnormal ovarian follicle number	J:6571
	abnormal spermatogenesis	J:6571
	absent coat pigmentation	J:6571
	infertility	J:6571
	prenatal lethality, incomplete penetrance	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-37J/KitW involves: C57BL/6 * C57BL/6J * WB	abnormal mast cell physiology	J:27513
	absent coat pigmentation	J:27513
	decreased mast cell number	J:27513
KitW-38H/Kit+ Not Specified	belly spot	J:180729
	head spot	J:180729
	white spotting	J:180729
KitW-38H/KitW-38H Not Specified	absent coat pigmentation	J:180729
KitW-38J/Kit+ involves: C57BL/6J	polycythemia	J:6571
	small testis	J:6571
KitW-38J/KitW-38J involves: C57BL/6J	perinatal lethality, complete penetrance	J:6571
	prenatal lethality, incomplete penetrance	J:6571
KitW-38J/KitW-39J involves: C57BL/6J	abnormal ovarian follicle number	J:6571
	abnormal spermatogenesis	J:6571
	absent coat pigmentation	J:6571
	infertility	J:6571
	prenatal lethality, incomplete penetrance	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-39H/Kit+ involves: BALB/cCrl * C3H/HeNCrl	abnormal coat/hair pigmentation	J:63816
	belly spot	J:63816, J:169366
	head blaze	J:169366
	white spotting	J:63816, J:169366
KitW-39H/KitW-39H involves: BALB/cCrl * C3H/HeNCrl	prenatal lethality, complete penetrance	J:169366
KitW-39J/Kit+ C57BL/6J-KitW-39J/J	belly spot	J:6571
	diluted coat color	J:6571
	macrocytic anemia	J:6571
KitW-39J/KitW-39J C57BL/6J-KitW-39J/J	abnormal ovarian follicle number	J:6571
	absent coat pigmentation	J:6571
	delayed female fertility	J:6571
	prenatal lethality, incomplete penetrance	J:6571
	reduced fertility	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-39J/KitW-40J involves: C57BL/6J	abnormal ovarian follicle number	J:6571
	abnormal spermatogenesis	J:6571
	absent coat pigmentation	J:6571
	infertility	J:6571
	prenatal lethality, incomplete penetrance	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-39J/KitW-41J involves: C57BL/6J	abnormal ovarian follicle number	J:6571
	absent coat pigmentation	J:6571
	prenatal lethality, incomplete penetrance	J:6571
	normal reproductive system phenotype	J:6571
	small ovary	J:6571
KitW-39J/KitW-42J involves: C57BL/6J	abnormal ovarian follicle number	J:6571
	abnormal spermatogenesis	J:6571
	absent coat pigmentation	J:6571
	infertility	J:6571
	prenatal lethality, incomplete penetrance	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-39J/KitW-43J involves: C57BL/6J	abnormal ovarian follicle number	J:6571
	abnormal spermatogenesis	J:6571
	absent coat pigmentation	J:6571
	infertility	J:6571
	prenatal lethality, incomplete penetrance	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-39J/KitW-44J involves: C3H/HeJ * C57BL/6J	abnormal ovarian follicle number	J:6571
	absent coat pigmentation	J:6571
	decreased litter size	J:6571
	male infertility	J:6571
	reduced female fertility	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-39J/KitW-v involves: C57BL * C57BL/6J	abnormal ovarian follicle number	J:6571
	absent coat pigmentation	J:6571
	delayed female fertility	J:6571
	reduced fertility	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-39J/KitW involves: C57BL/6J	abnormal ovarian follicle number	J:6571
	abnormal spermatogenesis	J:6571
	absent coat pigmentation	J:6571
	infertility	J:6571
	small ovary	J:6571
	small testis	J:6571
KitW-40H/KitW-40H involves: BALB/c * C3H/HeN	abnormal coat/hair pigmentation	J:63816
	white spotting	J:63816
KitW-40J/Kit+ C57BL/6J-KitW-40J/J	polycythemia	J:6571
	normal reproductive system phenotype	J:6571
	small testis	J:6571
KitW-40J/KitW-40J C57BL/6J-KitW-40J/J	perinatal lethality, complete penetrance	J:6571
	prenatal lethality, incomplete penetrance	J:6571
KitW-41J/Kit+ C57BL/6J-KitW-41J/J	belly spot	J:6571
	diluted coat color	J:6571
	macrocytic anemia	J:6571
KitW-41J/KitW-41J C57BL/6J-KitW-41J/J	abnormal ovarian follicle number	J:6571
	irregular coat pigmentation	J:6571
	macrocytic anemia	J:6571
	normal reproductive system phenotype	J:6571
	small ovary	J:6571
KitW-41J/KitW-44J involves: C3H/HeJ * C57BL/6J	abnormal ovarian follicle number	J:6571
	normal reproductive system phenotype	J:6571
	small ovary	J:6571
KitW-42J/Kit+ C57BL/6J-KitW-42J/J	abnormal ovarian follicle number	J:6571
	absent coat pigmentation	J:6571
	irregular coat pigmentation	J:6571
	macrocytic anemia	J:6571
	normal reproductive system phenotype	J:36829
	small testis	J:6571
KitW-42J/Kit+ involves: C57BL/6 * C57BL/6J * WB	decreased erythrocyte cell number	J:27513
	decreased mast cell number	J:27513
	diluted coat color	J:27513
	white spotting	J:27513
KitW-42J/KitW-42J C57BL/6J-KitW-42J/J	embryonic lethality during organogenesis, incomplete penetrance	J:36829
	macrocytic anemia	J:6571
	perinatal lethality, complete penetrance	J:6571
	normal reproductive system phenotype	J:36829
KitW-42J/KitW involves: C57BL/6 * C57BL/6J * WB	abnormal mast cell physiology	J:27513
	absent coat pigmentation	J:27513
	decreased mast cell number	J:27513
KitW-43J/Kit+ C57BL/6J-KitW-43J/J	polycythemia	J:6571
	small testis	J:6571
KitW-43J/KitW-43J C57BL/6J-KitW-43J/J	perinatal lethality	J:6571
KitW-44J/Kit+ B6.C3-KitW-44J/J	belly spot	J:6571
	normal hematopoietic system phenotype	J:6571
	white spotting	J:6571
KitW-44J/KitW-44J B6.C3-KitW-44J/J	abnormal ovarian follicle number	J:6571
	abnormal ovary morphology	J:6571
	decreased litter size	J:6571
	normal hematopoietic system phenotype	J:6571
	irregular coat pigmentation	J:6571
	male infertility	J:6571
	reduced female fertility	J:6571
	small ovary	J:6571
KitW-45J/Kit+ involves: DBA/2J	white spotting	J:78381
KitW-49J/Kit+ involves: C57BL/6J	white spotting	J:78381
KitW-51J/Kit+ involves: C57BL/6J	white spotting	J:78381
KitW-55J/Kit+ C57BL/6J-KitW-55J/J	anemia	J:28221
	white spotting	J:28221
KitW-55J/KitW-55J C57BL/6J-KitW-55J/J	absent coat pigmentation	J:28221
	anemia	J:28221
	female infertility	J:28221
	male infertility	J:28221
KitW-59J/Kit+ involves: C57BL/6J	white spotting	J:78381
KitW-70J/Kit+ involves: C57BL/6J	white spotting	J:78381
KitW-73J/Kit+ involves: DBA/2J	white spotting	J:16572
KitW-73J/KitW-73J involves: DBA/2J	anemia	J:16572
	postnatal lethality, complete penetrance	J:16572
	prenatal lethality, incomplete penetrance	J:16572
KitW-80J/Kit+ Not Specified	white spotting	J:78381
KitW-82J/Kit+ involves: C3HeB/FeLe	abnormal coat/hair pigmentation	J:75289
	abnormal skin pigmentation	J:75289
KitW-83J/KitW-v involves: DLS/LeJ * MWT/Le	absent coat pigmentation	J:28843
KitW-84J/Kit+ involves: 129S2/SvPas * C57BL/6J	white spotting	J:173520
KitW-85J/Kit+ C57BL/6J-KitW-85J/GrsrJ	normal hearing/vestibular/ear phenotype	J:212309
	white spotting	J:212309
KitW-85J/KitW-85J C57BL/6J-KitW-85J/GrsrJ	absent coat pigmentation	J:212309
KitW-a/Kit+ involves: Z	belly blaze	J:28886
	belly spot	J:28886
KitW-a/KitW-a involves: Z	anemia	J:28886
	postnatal lethality	J:28886
KitW-b/Kit+ involves: C57BL/St	diluted coat color	J:13078
	white spotting	J:13078
KitW-b/KitW-b involves: C57BL/St	absent coat pigmentation	J:13078
	anemia	J:13078
	decreased survivor rate	J:13078
	infertility	J:13078
	postnatal lethality	J:13078
KitW-b/KitW-s involves: BRS * C57BL/St	absent coat pigmentation	J:13078
	anemia	J:13078
KitW-Bs/Kit+ C57BL/6J-KitW-Bs	variable body spotting	J:157, J:238
KitW-Bs/KitW-Bs C57BL/6J-KitW-Bs	embryonic lethality, complete penetrance	J:157, J:238
KitW-Bs/KitW-v involves: C57BL/6J	abnormal coat/hair pigmentation	J:157
	anemia	J:157
KitW-Btlr/Kit+ C57BL/6J-KitW-Btlr	belly spot	J:133270
KitW-Btlr/KitW-Btlr C57BL/6J-KitW-Btlr	absent coat pigmentation	J:133270
	absent skin pigmentation	J:133270
	decreased mast cell number	J:133270
	infertility	J:133270
	normal pigmentation phenotype	J:133270
KitW-ct/Kit+ involves: 101/H * C3H/HeH	macrocytic anemia	J:7216
KitW-ct/KitW-ct involves: 101/H * C3H/HeH	absent coat pigmentation	J:7216
	anemia	J:7216
	postnatal lethality, complete penetrance	J:7216
	prenatal lethality, incomplete penetrance	J:7216
KitW-e/Kit+ involves: 101/H * C3H/HeH	diluted coat color	J:13765
	variable body spotting	J:13765
KitW-e/KitW-e involves: 101 * C3H	abnormal primordial germ cell migration	J:16216
	abnormal primordial germ cell morphology	J:16216
	decreased primordial germ cell proliferation	J:16216
KitW-e/KitW-e involves: 101/H * C3H/HeH	absent coat pigmentation	J:13765
	anemia	J:13765
	postnatal lethality, complete penetrance	J:13765
KitW-ei/Kit+ C57BL-KitW-ei	irregular coat pigmentation	J:28100
KitW-ei/KitW-ei C57BL-KitW-ei	abnormal coat/hair pigmentation	J:28100
	female infertility	J:28100
	male infertility	J:28100
	perinatal lethality, complete penetrance	J:28100
KitW-f/Kit+ involves: C3H/HePas	belly spot	J:6187
	diluted coat color	J:27513
	head spot	J:6187
	macrocytic anemia	J:6187
	non-pigmented tail tip	J:6187
KitW-f/KitW-f involves: C3H/HePas	decreased erythrocyte cell number	J:27513
	decreased mast cell number	J:27513
	diluted coat color	J:6187, J:27513
	irregular coat pigmentation	J:6187
	macrocytic anemia	J:6187
	postnatal lethality	J:6187
	normal reproductive system phenotype	J:6187
	white spotting	J:27513
KitW-j/Kit+ involves: C3H	white spotting	J:3398
KitW-j/KitW-j involves: C3H	abnormal spermatogenesis	J:3398
	absent coat pigmentation	J:3398
	anemia	J:3398
	postnatal lethality	J:3398
KitW-Jic/Kit+ involves: C57BL/6	decreased erythrocyte cell number	J:27513
	decreased mast cell number	J:27513
	diluted coat color	J:27513
	white spotting	J:27513
KitW-Jic/KitW involves: C57BL/6 * WB	abnormal mast cell physiology	J:27513
	absent coat pigmentation	J:27513
	decreased mast cell number	J:27513
KitW-n/Kit+ involves: WB	white spotting	J:27513
KitW-n/Kit+ Not Specified	diluted coat color	J:12107
	irregular coat pigmentation	J:12107
KitW-n/KitW-n Not Specified	absent coat pigmentation	J:12107
	decreased mast cell number	J:12107
	macrocytic anemia	J:12107
KitW-n/KitW involves: WB	abnormal mast cell physiology	J:27513
	absent coat pigmentation	J:27513
	decreased mast cell number	J:27513
KitW-pw/Kit+ involves: STOCK Prop1df Myo5ad Bmp5se	absent coat pigmentation	J:13655
	female infertility	J:13655
	male infertility	J:13655
	white spotting	J:13655
KitW-pw/KitW-pw involves: STOCK Prop1df Myo5ad Bmp5se	anemia	J:13655
	postnatal lethality	J:13655
KitW-pw/KitW-v involves: STOCK Prop1df Myo5ad Bmp5se	absent coat pigmentation	J:13655
	female infertility	J:13655
	male infertility	J:13655
KitW-rio/Kit+ DBA/2-KitW-rio	white spotting	J:29400
KitW-rio/Kit+ involves: C57BL/6 * DBA/2	reversion by mitotic recombination	J:29400
	white spotting	J:29400
KitW-rio/KitW-rio DBA/2-KitW-rio	macrocytic anemia	J:29400
	perinatal lethality, complete penetrance	J:29400
KitW-s/Kit+ involves: BRS	white spotting	J:15330
KitW-s/KitW-s involves: BRS	anemia	J:15330
	lethality throughout fetal growth and development, complete penetrance	J:15330
KitW-s/KitW involves: BRS	prenatal lethality, complete penetrance	J:15330
KitW-v/Kit+ involves: C57BL	diluted coat color	J:2447
	normal reproductive system phenotype	J:2447
	variable body spotting	J:2447
KitW-v/Kit+ involves: C57BL * C57BL/6	decreased erythrocyte cell number	J:27513
	decreased mast cell number	J:27513
	diluted coat color	J:27513
	white spotting	J:27513
KitW-v/Kit+ involves: C57BL * DBA	belly spot	J:125080
	diluted coat color	J:125080
	head spot	J:125080
	macrocytic anemia	J:125080
KitW-v/Kit+ involves: C57BL/6	macrocytic anemia	J:3400
KitW-v/Kit+ Not Specified	abnormal coat/hair pigmentation	J:2447
	diluted coat color	J:2447
	normal reproductive system phenotype	J:2447
	variable body spotting	J:2447
KitW-v/KitW-v C57BL/6J-KitW-v/J	decreased body weight	J:243758
	macrocytic anemia	J:243758
KitW-v/KitW-v involves: C57BL/6	increased bleeding time	J:7327
	macrocytic anemia	J:3400
KitW-v/KitW-v involves: CBA/Ca	abnormal ear pigmentation	J:4062
	abnormal melanocyte morphology	J:4062
	abnormal melanosome morphology	J:4062
	abnormal stria vascularis morphology	J:4062
	abnormal stria vascularis vasculature morphology	J:4062
	abnormal strial basal cell morphology	J:4062
	abnormal strial marginal cell morphology	J:4062
	absent endocochlear potential	J:4062
	absent strial intermediate cells	J:4062
	thin stria vascularis	J:4062
KitW-v/KitW-v Not Specified	abnormal coat/hair pigmentation	J:2447
	abnormal cochlea morphology	J:5179
	abnormal cochlear ganglion morphology	J:5179
	abnormal cochlear outer hair cell morphology	J:5179
	abnormal ear pigmentation	J:5179
	abnormal organ of Corti morphology	J:5179
	abnormal otolith morphology	J:5179
	abnormal stria vascularis morphology	J:5179
	abnormal stria vascularis vasculature morphology	J:5179
	abnormal tectorial membrane morphology	J:5179
	abnormal vestibular saccule morphology	J:5179
	cochlear ganglion degeneration	J:5179
	enlarged otoliths	J:5179
	reduced fertility	J:2447
	thin stria vascularis	J:5179
	vestibular hair cell degeneration	J:5179
KitW-vkd/KitW-vkd involves: 129P2/OlaHsd * BALB/c * C57BL/6 * WB	abnormal B cell differentiation	J:79128
	abnormal T cell differentiation	J:79128
	decreased B cell number	J:79128
	decreased bone marrow cell number	J:79128
	decreased thymocyte number	J:79128
	low mean erythrocyte cell number	J:79128
KitW-x/Kit+ involves: C3H/HeJ	abnormal coat/hair pigmentation	J:3398
KitW-x/KitW-x involves: C3H/HeJ	abnormal coat/hair pigmentation	J:3398
KitW/Kit+ FL/1Re-KitW/J	high mean erythrocyte cell number	J:24610
	increased hematocrit	J:24610
KitW/Kit+ Not Specified	abnormal coat/hair pigmentation	J:12955
	normal hematopoietic system phenotype	J:14978
	irregular coat pigmentation	J:12955
	normal reproductive system phenotype	J:14978
	variable body spotting	J:12955
KitW/KitW-v (WB KitW x B6.Cg-KitW-v)F1	abnormal body temperature	J:197334
	abnormal circulating histamine level	J:197334
	decreased susceptibility to induced arthritis	J:178942
	decreased susceptibility to type I hypersensitivity reaction	J:197334
KitW/KitW-v (WB/ReJ x C57BL/6J-KitW-v/J)F1-KitW/KitW-v/J	abnormal interferon level	J:131785
	abnormal interleukin level	J:131785
	abnormal renal glomerulus morphology	J:113500
	abnormal response to cardiac infarction	J:106065
	abnormal response/metabolism to endogenous compounds	J:123463
	decreased airway responsiveness	J:123463
	decreased inflammatory response	J:131785
	decreased vascular permeability	J:84660
	glomerular crescent	J:113500
	normal immune system phenotype	J:125656
	impaired neutrophil recruitment	J:123463
	increased erythrocyte protoporphyrin level	J:5985
	increased myocardial infarct size	J:106065
	increased susceptibility to induced morbidity/mortality	J:113500
	increased urine protein level	J:113500
	kidney inflammation	J:113500
KitW/KitW-v involves: C57BL	abnormal digestive system physiology	J:70182
	abnormal interstitial cell of Cajal morphology	J:70182
	abnormal muscle physiology	J:70182
	azoospermia	J:4972
KitW/KitW-v involves: C57BL * C57BL/6 * WB	abnormal response/metabolism to endogenous compounds	J:125964
	increased susceptibility to induced morbidity/mortality	J:125964
	increased susceptibility to xenobiotic induced morbidity/mortality	J:125964
KitW/KitW-v involves: C57BL/6	decreased basophil cell number	J:178942
	decreased mast cell number	J:178942
	normal immune system phenotype	J:178942
KitW/KitW-v involves: C57BL/6 * WB	abnormal response to transplant	J:6084
	increased esophageal papilloma incidence	J:6393
	increased papilloma incidence	J:6393
	peptic ulcer	J:6393
KitW/KitW-v involves: C57BL/6J	decreased body weight	J:243758
	hepatic steatosis	J:125831
	macrocytic anemia	J:243758
	preweaning lethality, incomplete penetrance	J:243758
KitW/KitW-v Not Specified	abnormal caput epididymis morphology	J:290452
	abnormal Sertoli cell morphology	J:210656
	epididymis degeneration	J:335479
KitW/KitW B6.Cg-KitW/J	abnormal survival	J:243758
	decreased body weight	J:243758
	macrocytic anemia	J:243758
	perinatal lethality, incomplete penetrance	J:243758
	prenatal lethality	J:243758
KitW/KitW Not Specified	abnormal eye pigmentation	J:12955
	absent coat pigmentation	J:12955
	macrocytic anemia	J:14978
	postnatal lethality, complete penetrance	J:12955
KitWads/Kit+ C57BL/6J-KitWads	belly spot	J:96391
	head spot	J:96391
	increased mean platelet volume	J:96391
	variable body spotting	J:96391
KitWads/Kit+ involves: C57BL/6J	abnormal seminiferous tubule morphology	J:163026
KitWads/KitWads C57BL/6J-KitWads	abnormal skin pigmentation	J:96391
	abnormal stria vascularis morphology	J:96391
	abnormal stria vascularis vasculature morphology	J:96391
	absent coat pigmentation	J:96391
	absent ovarian follicles	J:96391
	absent strial intermediate cells	J:96391
	arrest of spermatogenesis	J:96391
	cochlear hair cell degeneration	J:96391
	deafness	J:96391
	decreased erythrocyte cell number	J:96391
	decreased mast cell number	J:96391
	female infertility	J:96391
	increased Leydig cell number	J:96391
	increased mean corpuscular volume	J:96391
	increased mean platelet volume	J:96391
	increased or absent threshold for auditory brainstem response	J:96391
	macrocytic anemia	J:96391
	male infertility	J:96391
	organ of Corti degeneration	J:96391
	small ovary	J:96391
	small testis	J:96391
	thin stria vascularis	J:96391
	thrombocytosis	J:96391
KitWads/KitWps involves: C57BL/6J * CBA/CaJ	absent coat pigmentation	J:196572
KitWhc1/Kit+ involves: C3HeB/Fe * C57BL/6	belly spot	J:125831
	head blaze	J:125831
KitWhc1/KitWhc1 involves: C3HeB/Fe * C57BL/6	abnormal coat/hair pigmentation	J:125831
	abnormal erythrocyte morphology	J:125831
	decreased erythrocyte cell number	J:125831
	decreased hematocrit	J:125831
	hepatic steatosis	J:125831
	increased hemoglobin content	J:125831
	increased mean corpuscular volume	J:125831
	macrocytic anemia	J:125831
	postnatal lethality	J:125831
	normal reproductive system phenotype	J:125831
	slow postnatal weight gain	J:125831
KitWps/Kit+ involves: C57BL/6J * CBA/CaJ	belly spot	J:196572
KitWps/KitWps involves: C57BL/6J * CBA/CaJ	absent coat pigmentation	J:196572
	absent skin pigmentation	J:196572
	normal pigmentation phenotype	J:196572
	reduced female fertility	J:196572
	reduced male fertility	J:196572
Tg(Cma1-cre)ARoer/0 Tg(Kit*D814V)1Roer/0 involves: C57BL/6	colitis	J:169611
	increased mast cell number	J:169611
	increased skin tumor incidence	J:169611
Tg(Cma1-cre)ARoer/0 Tg(Kit*D814V)3Roer/0 involves: C57BL/6	increased mast cell number	J:169611
	increased skin tumor incidence	J:169611
Tg(CMV-cre)1Cgn/0 Tg(Kit*D814V)1Roer/0 involves: BALB/cJ * C57BL/6	abnormal erythrocyte physiology	J:169611
	abnormal erythropoiesis	J:169611
	abnormal liver morphology	J:169611
	decreased survivor rate	J:169611
	increased mast cell number	J:169611
	increased nucleated erythrocyte cell number	J:169611
	large intestinal inflammation	J:169611
	neonatal lethality, incomplete penetrance	J:169611
Tg(CMV-cre)1Cgn/0 Tg(Kit*D814V)3Roer/0 involves: BALB/cJ * C57BL/6	abnormal erythrocyte physiology	J:169611
	abnormal erythropoiesis	J:169611
	abnormal liver morphology	J:169611
	decreased survivor rate	J:169611
	increased mast cell number	J:169611
	increased nucleated erythrocyte cell number	J:169611
	neonatal lethality, incomplete penetrance	J:169611
Tg(Kit*D814V)1Roer/0 Commd10Tg(Vav1-icre)A2Kio/Commd10+ involves: C57BL/6 * C57BL/10 * CBA/Ca	neonatal lethality	J:169611
Tg(Kit*D814V)1Roer/0 Tg(Mx1-cre)1Cgn/0 involves: C57BL/6 * CBA	abnormal bone marrow cell physiology	J:169611
	abnormal feces composition	J:169611
	abnormal large intestine morphology	J:169611
	abnormal mast cell morphology	J:169611
	colitis	J:169611
	crypts of Lieberkuhn abscesses	J:169611
	diarrhea	J:169611
	enlarged spleen	J:169611
	increased chronic myelocytic leukemia incidence	J:169611
	increased leukemia incidence	J:169611
	increased mast cell number	J:169611
	increased skin tumor incidence	J:169611
	large intestinal inflammation	J:169611
	premature death	J:169611
	rectal prolapse	J:169611
	small intestinal inflammation	J:169611
	weight loss	J:169611
Tg(Kit*D814V)2Roer/0 Tg(Mx1-cre)1Cgn/0 involves: C57BL/6 * CBA	abnormal bone marrow cell physiology	J:169611
	abnormal feces composition	J:169611
	abnormal large intestine morphology	J:169611
	abnormal mast cell morphology	J:169611
	colitis	J:169611
	crypts of Lieberkuhn abscesses	J:169611
	diarrhea	J:169611
	increased mast cell number	J:169611
	increased skin tumor incidence	J:169611
	large intestinal inflammation	J:169611
	rectal prolapse	J:169611
	small intestinal inflammation	J:169611
	weight loss	J:169611
Tg(Kit*D814V)3Roer/0 Commd10Tg(Vav1-icre)A2Kio/Commd10+ involves: C57BL/6 * C57BL/10 * CBA/Ca	neonatal lethality	J:169611
Tg(Kit*D814V)3Roer/0 Tg(Mx1-cre)1Cgn/0 involves: C57BL/6 * CBA	abnormal bone marrow cell physiology	J:169611
	abnormal feces composition	J:169611
	abnormal mast cell morphology	J:169611
	colitis	J:169611
	diarrhea	J:169611
	enlarged spleen	J:169611
	increased leukemia incidence	J:169611
	increased mast cell number	J:169611
	increased skin tumor incidence	J:169611
	large intestinal inflammation	J:169611
	premature death	J:169611
	rectal prolapse	J:169611
	weight loss	J:169611