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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Kitl
kit ligand
MGI:96974
96 phenotypes from 54 alleles in 49 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
KitlM1Bao/Kitl+
involves: C57BL/6J 		abnormal foot pigmentation J:164566
abnormal tail hair pigmentation J:164566
belly spot J:164566
white spotting J:164566
KitlM1Bao/KitlM1Bao
involves: C57BL/6J 		abnormal coat/hair pigmentation J:164566
Kitlm1Btlr/Kitlm1Btlr
C57BL/6J-Kitlm1Btlr 		absent coat pigmentation J:265121
irregular coat pigmentation J:265121
Kitlm2Btlr/Kitlm2Btlr
C57BL/6J-Kitlm2Btlr 		abnormal ventral coat pigmentation J:265215
belly spot J:265215
diluted coat color J:265215
KitlSl-1Neu/Kitl+
involves: 102/El * C3H/El 		belly spot J:37172
decreased erythrocyte cell number J:37172
decreased hematocrit J:37172
decreased hemoglobin content J:37172
decreased mean corpuscular hemoglobin concentration J:37172
diluted coat color J:37172
head spot J:37172
increased mean corpuscular hemoglobin J:37172
increased mean corpuscular volume J:37172
macrocytic anemia J:37172
KitlSl-1Neu/KitlSl-1Neu
involves: 102/El * C3H/El 		decreased erythrocyte cell number J:37172
decreased hematocrit J:37172
decreased hemoglobin content J:37172
decreased mean corpuscular hemoglobin concentration J:37172
diluted coat color J:37172
increased ear pigmentation J:37172
increased mean corpuscular hemoglobin J:37172
increased mean corpuscular volume J:37172
macrocytic anemia J:37172
reduced female fertility J:37172
KitlSl-2Neu/Kitl+
involves: 102/El * C3H/El 		decreased hematocrit J:37172
decreased hemoglobin content J:37172
diluted coat color J:37172
head spot J:37172
KitlSl-2Neu/KitlSl-2Neu
involves: 102/El * C3H/El 		decreased hematocrit J:37172
decreased hemoglobin content J:37172
diluted coat color J:37172
female infertility J:37172
reduced male fertility J:37172
KitlSl-3Neu/Kitl+
involves: 102/El * C3H/El 		diluted coat color J:43966
KitlSl-3Neu/KitlSl-3Neu
involves: 102/El * C3H/El 		diluted coat color J:43966
normal hematopoietic system phenotype J:43966
increased ear pigmentation J:43966
reduced female fertility J:43966
white spotting J:43966
KitlSl-3R/Kitl+
involves: 101/Rl * C3H/Rl 		diluted coat color J:100221
KitlSl-3R/KitlSl-3R
involves: 101/Rl * C3H/Rl 		prenatal lethality, complete penetrance J:100221
KitlSl-3R/KitlSl-12R
involves: 101/Rl * C3H/Rl 		absent coat pigmentation J:100221
female infertility J:100221
premature death J:100221
KitlSl-5R/Kitl+
C3.Cg-KitlSl-5R 		decreased erythrocyte cell number J:82263
KitlSl-5R/KitlSl-5R
C3.Cg-KitlSl-5R 		low mean erythrocyte cell number J:82263
perinatal lethality, incomplete penetrance J:82263
postnatal lethality, complete penetrance J:82263
KitlSl-5R/KitlSl-5R
C3H-KitlSl-5R 		decreased primordial germ cell number J:115437
KitlSl-12R/Kitl+
involves: 101/Rl * C3H/Rl 		decreased litter size J:100221
diluted coat color J:100221
KitlSl-12R/KitlSl-12R
involves: 101/Rl * C3H/Rl 		absent coat pigmentation J:100221
female infertility J:100221
premature death J:100221
KitlSl-13H/Kitl+
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:179353
abnormal tail hair pigmentation J:179353
belly spot J:179353
head spot J:179353
KitlSl-13H/KitlSl-13H
involves: 101/H * C3H/HeH 		postnatal lethality J:179353
KitlSl-15H/Kitl+
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:179353
abnormal tail hair pigmentation J:179353
belly spot J:179353
head spot J:179353
KitlSl-15H/KitlSl-15H
involves: 101/H * C3H/HeH 		postnatal lethality J:179353
KitlSl-16J/Kitl+
involves: 129 * Lipari 		diluted coat color J:30778
white spotting J:30778
KitlSl-17H/Kitl+
C3H/HeH-KitlSl-17H 		belly spot J:24739
decreased primordial germ cell number J:2880
diluted coat color J:24739
head spot J:24739
irregular coat pigmentation J:24739
white spotting J:24739
KitlSl-17H/KitlSl-17H
C3H/HeH-KitlSl-17H 		abnormal spermatogenesis J:2880
absent coat pigmentation J:24739
decreased male germ cell number J:2880
decreased oocyte number J:2880
decreased primordial germ cell number J:2880, J:115437
increased adenoma incidence J:2880
increased Leydig cell number J:2880
male infertility J:2880
small ovary J:2880
KitlSl-17H/KitlSl-con
involves: C3H/HeH 		diluted coat color J:24739
white spotting J:24739
KitlSl-18R/Kitl+
C3.Cg-KitlSl-18R 		decreased erythrocyte cell number J:82263
KitlSl-18R/KitlSl-18R
C3.Cg-KitlSl-18R 		low mean erythrocyte cell number J:82263
perinatal lethality, incomplete penetrance J:82263
postnatal lethality, complete penetrance J:82263
KitlSl-19J/KitlSl-19J
C3HeB/FeJ-KitlSl-19J 		absent coat pigmentation J:78803
KitlSl-20J/Kitl+
C57BL/6J-KitlSl-20J/J 		belly spot J:86436
KitlSl-20J/KitlSl-20J
C57BL/6J-KitlSl-20J/J 		abnormal erythropoiesis J:86436
absent primordial germ cells J:86436
decreased fetal size J:86436
lethality throughout fetal growth and development, complete penetrance J:86436
pale liver J:86436
pallor J:86436
KitlSl-21H/Kitl+
involves: C3H/HeH 		abnormal coat/hair pigmentation J:179353
abnormal tail hair pigmentation J:179353
belly spot J:179353
head spot J:179353
KitlSl-21H/KitlSl-21H
involves: C3H/HeH 		anemia J:179353
postnatal lethality, complete penetrance J:179353
KitlSl-21J/Kitl+
B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ 		abnormal foot pigmentation J:107116
belly spot J:107116
decreased ear pigmentation J:107116
decreased tail pigmentation J:107116
diluted coat color J:107116
KitlSl-22J/Kitl+
C57BL/6J-KitlSl-22J/GrsrJ 		abnormal foot pigmentation J:117733
abnormal retina pigmentation J:117733
belly spot J:117733
decreased ear pigmentation J:117733
decreased tail pigmentation J:117733
diluted coat color J:117733
normal hearing/vestibular/ear phenotype J:117733
normal vision/eye phenotype J:117733
KitlSl-22R/Kitl+
C3H-KitlSl-22R 		abnormal ventral coat pigmentation J:79293
head spot J:79293
normal hematopoietic system phenotype J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular volume J:79293
macrocytic anemia J:79293
KitlSl-22R/KitlSl-22R
C3H-KitlSl-22R 		decreased primordial germ cell number J:115437
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
perinatal lethality, incomplete penetrance J:79293
postnatal lethality, complete penetrance J:79293
prenatal lethality, incomplete penetrance J:79293
KitlSl-23J/Kitl+
B6Smn(C3)-KitlSl-23J/J 		belly spot J:121474
diluted coat color J:121474
Kitlsl-24J/Kitlsl-24J
B6;129S1-a Kitlsl-24J/GrsrJ 		decreased body size J:181680
decreased foot pigmentation J:181680
decreased tail pigmentation J:181680
normal reproductive system phenotype J:181680
variable body spotting J:181680
KitlSl-26H/Kitl+
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:179353
diluted coat color J:179353
head spot J:179353
KitlSl-27H/Kitl+
involves: C3H/HeH 		abnormal coat/hair pigmentation J:179353
diluted coat color J:179353
KitlSl-27H/KitlSl-27H
involves: C3H/HeH 		prenatal lethality, complete penetrance J:179353
KitlSl-28R/Kitl+
C3.101Rl-KitlSl-28R 		abnormal ventral coat pigmentation J:79293
head spot J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular volume J:79293
macrocytic anemia J:79293
KitlSl-28R/KitlSl-28R
C3.101Rl-KitlSl-28R 		decreased primordial germ cell number J:115437
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
perinatal lethality, incomplete penetrance J:79293
postnatal lethality, complete penetrance J:79293
prenatal lethality, incomplete penetrance J:79293
KitlSl-29H/Kitl+
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:169366
abnormal hind foot hair pigmentation J:169366
head spot J:169366
KitlSl-29H/KitlSl-29H
involves: 101/H * C3H/HeH 		absent coat pigmentation J:169366
KitlSl-30H/Kitl+
involves: 101/H * C3H/HeH 		abnormal tail hair pigmentation J:179353
diluted coat color J:179353
KitlSl-30H/KitlSl-30H
involves: 101/H * C3H/HeH 		embryonic lethality, complete penetrance J:179353
KitlSl-30R/Kitl+
C3.101Rl-KitlSl-30R 		abnormal ventral coat pigmentation J:79293
decreased hematocrit J:79293
head spot J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular volume J:79293
macrocytic anemia J:79293
KitlSl-30R/KitlSl-30R
C3.101Rl-KitlSl-30R 		decreased primordial germ cell number J:115437
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
postnatal lethality J:79293
KitlSl-31H/Kitl+
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:179353
belly spot J:179353
KitlSl-31H/KitlSl-31H
involves: 101/H * C3H/HeH 		perinatal lethality, complete penetrance J:179353
prenatal lethality, incomplete penetrance J:179353
KitlSl-31R/Kitl+
C3H-KitlSl-31R 		abnormal ventral coat pigmentation J:79293
head spot J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular volume J:79293
macrocytic anemia J:79293
KitlSl-31R/KitlSl-31R
C3H-KitlSl-31R 		decreased primordial germ cell number J:115437
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
perinatal lethality, incomplete penetrance J:79293
postnatal lethality, complete penetrance J:79293
prenatal lethality, incomplete penetrance J:79293
KitlSl-33H/Kitl+
involves: 101/H * C3H/HeH 		abnormal coat/hair pigmentation J:179353
abnormal tail hair pigmentation J:179353
KitlSl-34H/Kitl+
involves: 101/H * C3H/HeH 		diluted coat color J:44592
white spotting J:44592
KitlSl-34H/KitlSl-34H
involves: 101/H * C3H/HeH 		anemia J:44592
embryonic lethality, complete penetrance J:44592
KitlSl-35H/KitlSl-35H
involves: BALB/c * C3H/HeN 		diluted coat color J:63816
KitlSl-36H/KitlSl-36H
involves: BALB/c * C3H/HeN 		diluted coat color J:63816
KitlSl-36R/Kitl+
C3H-KitlSl-36R 		abnormal ventral coat pigmentation J:79293
head spot J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular volume J:79293
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
KitlSl-36R/KitlSl-36R
C3H-KitlSl-36R 		abnormal primordial germ cell migration J:115437
decreased hematocrit J:79293
decreased primordial germ cell number J:115437
decreased primordial germ cell proliferation J:115437
decreased survivor rate J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular hemoglobin concentration J:79293
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
postnatal lethality, incomplete penetrance J:79293
KitlSl-37H/KitlSl-37H
involves: BALB/c * C3H/HeN 		diluted coat color J:63816
KitlSl-38H/KitlSl-38H
involves: BALB/c * C3H/HeN 		diluted coat color J:63816
KitlSl-39R/Kitl+
C3.B10Rl-KitlSl-39R 		abnormal ventral coat pigmentation J:79293
head spot J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular volume J:79293
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
KitlSl-39R/KitlSl-39R
C3.B10Rl-KitlSl-39R 		abnormal coat/hair pigmentation J:79293
abnormal primordial germ cell migration J:115437
abnormal primordial germ cell morphology J:115437
decreased hematocrit J:79293
decreased primordial germ cell number J:115437
decreased primordial germ cell proliferation J:115437
decreased survivor rate J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular hemoglobin concentration J:79293
increased mean corpuscular volume J:79293
increased primordial germ cell apoptosis J:115437
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
postnatal lethality, incomplete penetrance J:79293
KitlSl-42R/Kitl+
C3.101Rl-KitlSl-42R 		abnormal ventral coat pigmentation J:79293
decreased hematocrit J:79293
head spot J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular volume J:79293
macrocytic anemia J:79293
KitlSl-42R/KitlSl-42R
C3.101Rl-KitlSl-42R 		decreased primordial germ cell number J:115437
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
perinatal lethality, incomplete penetrance J:79293
postnatal lethality, complete penetrance J:79293
prenatal lethality, incomplete penetrance J:79293
Kitlsl-blz/Kitlsl-blz
WSB/EiJ 		belly spot J:179958
diluted coat color J:179958
head blaze J:179958
KitlSl-Clo/Kitl+
Not Specified 		abnormal coat/hair pigmentation J:13613
diluted coat color J:13613
KitlSl-Clo/KitlSl-Clo
Not Specified 		abnormal coat/hair pigmentation J:13613
diluted coat color J:13613
reduced fertility J:13613
vagina atresia J:13654
variable body spotting J:13613
KitlSl-con/Kitl+
either: (involves: C3H/HeJ) or (involves: C3H/HeN) 		abnormal ovarian folliculogenesis J:23593
abnormal skin pigmentation J:23593
decreased oocyte number J:23593
hyperpigmentation J:23593
normal reproductive system phenotype J:23593
KitlSl-con/KitlSl-con
either: (involves: C3H/HeJ) or (involves: C3H/HeN) 		abnormal coat/hair pigmentation J:23593
abnormal skin pigmentation J:23593
decreased oocyte number J:23593
hyperpigmentation J:23593
impaired ovarian folliculogenesis J:23593
increased mast cell number J:23593
normal reproductive system phenotype J:23593
KitlSl-d/Kitl+
C3.D2-KitlSl-d 		abnormal ventral coat pigmentation J:79293
head spot J:79293
increased mean corpuscular hemoglobin J:79293
increased mean corpuscular volume J:79293
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
KitlSl-d/Kitl+
either: (involves: C57BL/6 * DBA/2J) or (involves: C3H * C57BL/6 * DBA/2J * WC) 		anemia J:6084
decreased mast cell number J:6084
KitlSl-d/Kitl+
either: DBA/2J or (C57BL/6 x DBA/2)F1 		diluted coat color J:13392
KitlSl-d/Kitl+
involves: DBA/2J 		diluted coat color J:125080
macrocytic anemia J:125080
KitlSl-d/KitlSl-18J
involves: C3H/HeJ * C57BL/6J * DBA/2J 		absent coat pigmentation J:78805
KitlSl-d/KitlSl-d
C3.D2-KitlSl-d 		abnormal primordial germ cell migration J:115437
abnormal primordial germ cell morphology J:115437
decreased hematocrit J:79293
decreased primordial germ cell number J:115437
decreased primordial germ cell proliferation J:115437
increased mean corpuscular hemoglobin concentration J:79293
increased mean corpuscular volume J:79293
increased primordial germ cell apoptosis J:115437
low mean erythrocyte cell number J:79293
macrocytic anemia J:79293
normal mortality/aging J:79293
KitlSl-d/KitlSl-d
either: DBA/2J or (C57BL/6 x DBA/2)F1 		abnormal coat/hair pigmentation J:13392, J:20286
anemia J:13392, J:20286
infertility J:13392, J:20286
KitlSl-d/KitlSl-d
Not Specified 		abnormal melanoblast morphology J:31646
Kitlsl-du/Kitlsl-du
C3H/HeJ-Kitlsl-du 		anemia J:13630
diluted coat color J:13630
variable body spotting J:13630
KitlSl-m/Kitl+
involves: C57BL/6 		abnormal coat/hair pigmentation J:13416
diluted coat color J:13416
KitlSl-m/KitlSl-m
involves: C57BL/6 		abnormal coat/hair pigmentation J:13416
absent coat pigmentation J:13416
anemia J:5009, J:13416
gastrointestinal hemorrhage J:5009
male infertility J:13416
premature death J:5009, J:13416
reduced female fertility J:13137, J:13416
KitlSl-so/Kitl+
involves: C57BL/6 		abnormal coat/hair pigmentation J:13416
abnormal tail hair pigmentation J:13416
diluted coat color J:13416
KitlSl-so/KitlSl-so
involves: C57BL/6 		abnormal coat/hair pigmentation J:13416
absent coat pigmentation J:13416
anemia J:13416
postnatal lethality, complete penetrance J:13416
KitlSl-t/Kitl+
B6.Cg-KitlSl-t 		diluted coat color J:81273
non-pigmented tail tip J:81273
KitlSl-t/KitlSl-t
B6.Cg-KitlSl-t 		absent coat pigmentation J:81273
KitlSl-t/KitlSl-t
WB.Cg-KitlSl-t 		absent coat pigmentation J:81274
head spot J:81274
Kitltm1.1Sjm/Kitl+
BKa.129S6-Kitltm1.1Sjm 		liver hypoplasia J:180431
Kitltm1.1Sjm/Kitltm1.1Sjm
BKa.129S6-Kitltm1.1Sjm 		abnormal bone marrow cell physiology J:180431
anemia J:180431
decreased erythrocyte cell number J:180431
decreased hematopoietic cell number J:180431
liver hypoplasia J:180431
perinatal lethality, complete penetrance J:180431
Kitltm1.1Sjm/Kitltm2.1Sjm
Leprtm2(cre)Rck/Lepr+
involves: 129S6/SvEvTac * C57BL/6 * C57BL/Ka * SJL 		decreased hematopoietic cell number J:180431
enlarged spleen J:180431
extramedullary hematopoiesis J:180431
spleen hyperplasia J:180431
Kitltm1.1Sjm/Kitltm2.1Sjm
Leprtm2(cre)Rck/Lepr+
Tg(Tek-cre)12Flv/0
involves: 129S6/SvEvTac * C3H * C57BL/6 * C57BL/Ka * SJL 		decreased bone marrow cell number J:180431
decreased hematopoietic cell number J:180431
spleen hyperplasia J:180431
Kitltm1Pbes/Kitltm1Pbes
involves: 129S1/Sv * C57BL/6J 		abnormal blood homeostasis J:50150
decreased mast cell number J:50150
normal hematopoietic system phenotype J:50150
increased mortality induced by ionizing radiation J:50150
Kitltm2.1Pbes/Kitltm2.1Pbes
involves: 129S1/Sv * C57BL/6J * FVB/N 		abnormal common myeloid progenitor cell morphology J:157170
decreased cell proliferation J:157170
decreased testis weight J:157170
increased mast cell number J:157170
Kitltm2.1Sjm/Kitltm2.1Sjm
Ndor1Tg(UBC-cre/ERT2)1Ejb/0
involves: 129S/SvEv * C57BL/6 * C57BL/Ka * SJL 		abnormal bone marrow cell physiology J:180431
anemia J:180431
decreased bone marrow cell number J:180431
decreased erythrocyte cell number J:180431
decreased hematopoietic cell number J:180431
liver hypoplasia J:180431
Kitltm2.1Sjm/Kitltm2.2Sjm
Commd10Tg(Vav1-icre)A2Kio/Commd10+
involves: BALB/cJ * C57BL * CBA/Ca * SJL 		decreased hematopoietic cell number J:180431
normal hematopoietic system phenotype J:180431
Kitltm2.1Sjm/Kitltm2.2Sjm
Tg(Col1a1-cre)2Bek/0
involves: BALB/cJ * C57BL/6 * C57BL/Ka * CD-1 * SJL 		decreased hematopoietic cell number J:180431
normal hematopoietic system phenotype J:180431
Kitltm2.1Sjm/Kitltm2.2Sjm
Tg(Nes-cre)1Kln/0
involves: BALB/cJ * C57BL/6 * C57BL/Ka * SJL 		normal hematopoietic system phenotype J:180431
Kitltm2.1Sjm/Kitltm2.2Sjm
Tg(Nes-cre/ERT2)1Fsh/0
involves: BALB/cJ * C57BL/6 * C57BL/Ka * FVB/N * SJL 		normal hematopoietic system phenotype J:180431
Kitltm2.1Sjm/Kitltm2.2Sjm
Tg(Tek-cre)12Flv/0
involves: BALB/cJ * C3H * C57BL/6 * C57BL/Ka * SJL 		abnormal bone marrow cell physiology J:180431
decreased hematopoietic cell number J:180431
normal hematopoietic system phenotype J:180431
Kitltm2.2Sjm/Kitl+
involves: BALB/cJ * C57BL/6 * C57BL/Ka * SJL 		decreased hematopoietic cell number J:180431
Kitltm2.2Sjm/Kitltm2.2Sjm
involves: BALB/cJ * C57BL/6 * C57BL/Ka * SJL 		anemia J:180431
perinatal lethality, complete penetrance J:180431
Kitltm3.1Pbes/Kitl+
involves: 129S1/Sv * C57BL/6J * FVB/N 		belly spot J:157170
Kitltm3.1Pbes/Kitltm3.1Pbes
involves: 129S1/Sv * C57BL/6J * FVB/N 		abnormal bone marrow cell physiology J:157170
absent coat pigmentation J:157170
azoospermia J:157170
decreased double-negative T cell number J:157170
decreased double-positive T cell number J:157170
decreased erythrocyte cell number J:157170
decreased mast cell number J:157170
decreased T cell number J:157170
decreased testis weight J:157170
decreased thymocyte number J:157170
early reproductive senescence J:157170
increased mean corpuscular volume J:157170
reduced male fertility J:157170
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)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory