About   Help   FAQ
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
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support. 		last database update
12/17/2024
MGI 6.24 		The Jackson Laboratory