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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Kit
KIT proto-oncogene receptor tyrosine kinase
MGI:96677
242 phenotypes from 90 alleles in 90 genetic backgrounds
Export: Excel File
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
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11/12/2024
MGI 6.24 		The Jackson Laboratory