96 phenotypes from 54 alleles in 49 genetic backgrounds

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