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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Mitf
melanogenesis associated transcription factor
MGI:104554
129 phenotypes from 38 alleles in 39 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background		 Annotated Term Reference
MitfMi-b/Mitf+
involves: 101/Rl * C3H/Rl 		abnormal choroid pigmentation J:37067
abnormal eye pigmentation J:37067
abnormal Harderian gland pigmentation J:37067
decreased ear pigmentation J:37067
decreased tail pigmentation J:37067
diluted coat color J:37067
MitfMi-b/MitfMi-b
involves: 101/Rl * C3H/Rl 		abnormal choroid pigmentation J:37067
abnormal ciliary process morphology J:37067
abnormal eye physiology J:37067
abnormal eye pigmentation J:37067
abnormal Harderian gland pigmentation J:37067
abnormal retina morphology J:37067
abnormal retina pigment epithelium morphology J:37067
absent coat pigmentation J:37067
increased susceptibility to age-related retinal degeneration J:37067
MitfMi-b/MitfMi-Or
involves: 101/Rl * C3H/Rl 		absent coat pigmentation J:15061
decreased eye pigmentation J:15061
MitfMi-b/MitfMi-wh
involves: 101/Rl * C3H/Rl 		abnormal coat/hair pigmentation J:15061
decreased eye pigmentation J:15061
variable body spotting J:15061
Mitfmi-bw/Mitfmi-bw
involves: C3H 		abnormal hearing physiology J:21682
abnormal stria vascularis morphology J:21682
absent coat pigmentation J:13071
absent strial intermediate cells J:21682
increased or absent threshold for auditory brainstem response J:21682
thin stria vascularis J:21682
Mitfmi-bw/Mitfmi-bw
Tg(Dct-lacZ)A12Jkn/0
involves: C3H * C57BL/6 * C57BL/6J * CBA 		abnormal melanoblast migration J:213982
abnormal melanoblast morphology J:213982
absent coat pigmentation J:213982
absent hair follicle melanin granules J:213982
decreased melanocyte number J:213982
Mitfmi-bws/Mitfmi-bws
BKS.Cg-m+/+Leprdb 		white spotting J:45568
Mitfmi-ce/Mitfmi-ce
involves: DBA/2N 		abnormal cochlear hair cell morphology J:34879
abnormal estrous cycle J:34879
abnormal eye development J:34879
abnormal eye pigmentation J:34879
abnormal fertility/fecundity J:34879
abnormal inner ear morphology J:34879
abnormal lens morphology J:34879
cataract J:34879
decreased eye pigmentation J:34879
microphthalmia J:34879
thin stria vascularis J:34879
MitfMi-Crc/Mitf+
involves: CBA/CaCrc 		abnormal iris pigmentation J:83500
non-pigmented tail tip J:83500
variable body spotting J:83500
MitfMi-Crc/MitfMi-Crc
involves: CBA/CaCrc 		absent coat pigmentation J:83500
decreased eye pigmentation J:83500
eyelids fail to open J:83500
failure of tooth eruption J:83500
female infertility J:83500
male infertility J:83500
microphthalmia J:83500
osteopetrosis J:83500
Mitfmi-di/Mitfmi-di
(PT x C3H/HeH)F1 		abnormal photoreceptor inner segment morphology J:8196
abnormal retina development J:8196
abnormal retina photoreceptor morphology J:8196
abnormal spleen germinal center morphology J:8196
abnormal spleen morphology J:8196
abnormal spleen red pulp morphology J:8196
abnormal spleen white pulp morphology J:8196
abnormal vitreous body morphology J:8196
absent coat pigmentation J:8196
absent photoreceptor outer segment J:8196
decreased eye pigmentation J:8196
microphthalmia J:8196
osteopetrosis J:8196
Mitfmi-enu5/Mitf+
involves: 102 * C3H/El 		absent pinna reflex J:89276
belly spot J:89276
diluted coat color J:89276
head spot J:89276
normal skeleton phenotype J:89276
white spotting J:89276
Mitfmi-enu5/Mitfmi-enu5
involves: 102 * C3H/El 		abnormal nursing J:89276
abnormal pinna reflex J:89276
absent coat pigmentation J:89276
absent pinna reflex J:89276
female infertility J:89276
male infertility J:89276
microphthalmia J:89276
normal skeleton phenotype J:89276
Mitfmi-enu22(398)/Mitfmi-enu22(398)
Not Specified 		belly spot J:154486
normal vision/eye phenotype J:154486
white spotting J:154486
Mitfmi-enu122/Mitf+
involves: 102 * C3H 		abnormal retina pigmentation J:46254
Mitfmi-enu122/Mitfmi-enu122
involves: 102 * C3H 		abnormal foot pigmentation J:46254
decreased eye pigmentation J:46254, J:63651
decreased tail pigmentation J:46254
irregular coat pigmentation J:46254
microphthalmia J:46254
Mitfmi-enu198/Mitf+
involves: 102 * C3H 		decreased eye pigmentation J:62098
Mitfmi-enu198/Mitfmi-enu198
involves: 102 * C3H 		absent coat pigmentation J:62098
absent eye pigmentation J:62098
microphthalmia J:62098
Mitfmi-ew/Mitfmi-ew
involves: C57BL/6Bn * NAW 		absent coat pigmentation J:89821
exostosis J:89821
microphthalmia J:89821
osteopetrosis J:89821
Mitfmi-ew/Mitftm1Arnh
involves: 129S1/Sv * C57BL/6 * NAW 		absent coat pigmentation J:130168
normal vision/eye phenotype J:130168
MitfMi-H/Mitf+
involves: BALB/cAnN * C3H/HeN 		abnormal coat/hair pigmentation J:75964
abnormal foot pigmentation J:75964
abnormal iris morphology J:75964
decreased ear pigmentation J:75964
decreased tail pigmentation J:75964
irregular coat pigmentation J:75964
MitfMi-H/MitfMi-H
involves: BALB/cAnN * C3H/HeN 		abnormal coat/hair pigmentation J:75964
abnormal eye morphology J:75964
abnormal skin pigmentation J:75964
absent coat pigmentation J:75964
anophthalmia J:75964
MitfMi-H/MitfRorp
involves: BALB/cAnN * C3H/HeN 		abnormal coat/hair pigmentation J:75964
abnormal iris pigmentation J:75964
abnormal ocular fundus morphology J:75964
absent coat pigmentation J:75964
coloboma J:75964
mydriasis J:75964
MitfMi-Mee/?
involves: C57BL/6 * CAST * FVB 		abnormal retina pigmentation J:140311
decreased eye pigmentation J:140311
MitfMi-Mee/Mitf+
involves: C57BL/6 * FVB 		abnormal retina pigmentation J:140311
decreased eye pigmentation J:140311
MitfMi-Mee/MitfMi-Mee
involves: C57BL/6 * FVB 		abnormal iris pigmentation J:140311
abnormal lens morphology J:140311
abnormal optic cup morphology J:140311
abnormal retina morphology J:140311
abnormal retina pigmentation J:140311
absent coat pigmentation J:140311
decreased eye pigmentation J:140311
impaired pupillary reflex J:140311
lens vacuoles J:140311
Mitfmi-Mhdabcc2/Mitf+
C3HeB/FeJ-Mitfmi-Mhdabcc2/Ieg 		belly spot J:89276
diluted coat color J:89276
head spot J:89276
white spotting J:89276
Mitfmi-Mhdabcc2/Mitfmi-Mhdabcc2
C3HeB/FeJ-Mitfmi-Mhdabcc2/Ieg 		abnormal nursing J:89276
absent coat pigmentation J:89276
female infertility J:89276
male infertility J:89276
microphthalmia J:89276
MitfMi-Or/Mitf+
involves: 101/Rl * C3H/Rl 		belly spot J:13426, J:30149
decreased ear pigmentation J:13426
decreased eye pigmentation J:13426
decreased tail pigmentation J:13426
diluted coat color J:13426, J:30149
head spot J:13426
MitfMi-Or/MitfMi-Or
involves: 101/Rl * C3H/Rl 		abnormal epiphyseal plate morphology J:30149
abnormal incisor morphology J:13426
abnormal long bone epiphyseal plate morphology J:30149
abnormal long bone metaphysis morphology J:30149
abnormal osteoclast morphology J:30149
abnormal osteoclast physiology J:30149
absent coat pigmentation J:13426, J:30149, J:89821
anophthalmia J:13426
decreased eye pigmentation J:13426, J:30149
decreased length of long bones J:30149
decreased osteoclast cell number J:30149
eyelids fail to open J:13426
failure of tooth eruption J:13426, J:89821
female infertility J:13426
increased osteoclast cell number J:30149
increased trabecular bone connectivity density J:30149
increased width of hypertrophic chondrocyte zone J:30149
microphthalmia J:13426, J:89821
osteopetrosis J:30149, J:89821
osteosclerosis J:30149
premature death J:13426
Mitfmi-rw/Mitfmi-rw
involves: CBA/J 		abnormal coat/hair pigmentation J:13661, J:132153
abnormal eye pigmentation J:13661
abnormal eye size J:13661
decreased eye pigmentation J:13661
microphthalmia J:13661
Mitfmi-sp/Mitfmi-sp
B6.Cg-MitfMi-wh/Mitfmi-sp/J 		hypopigmentation J:12946
normal pigmentation phenotype J:12946, J:35685
Mitfmi-tg/Mitf+
involves: C3H/HeNCrl * C57BL/6NCrl 		abnormal melanocyte morphology J:15418
Mitfmi-tg/Mitfmi-tg
B6.Cg-Mitfmi-tg 		abnormal mast cell physiology J:53161
absent coat pigmentation J:53161
decreased serotonin level J:53161
Mitfmi-tg/Mitfmi-tg
involves: C3H/HeNCrl * C57BL/6NCrl 		abnormal hair follicle melanocyte morphology J:15418
abnormal iris pigmentation J:16790
abnormal melanocyte morphology J:15418
absent coat pigmentation J:15418
ciliary body hypoplasia J:16790
iris hypoplasia J:16790
microphthalmia J:15418
Mitfmi-vga9/Mitfmi-vga9
involves: C57BL/6 * CBA 		abnormal retina pigment epithelium morphology J:188155
absent coat pigmentation J:89821
microphthalmia J:89821
Mitfmi-vga9/Mitftm1Arnh
involves: 129S1/Sv * C3H/He * C57BL/6 		absent coat pigmentation J:130168
normal vision/eye phenotype J:130168
Mitfmi-vit/Mitfmi-vit
C57BL/6J-Mitfmi-vit 		abnormal hair follicle morphology J:102101
abnormal Langerhans cell physiology J:102101
abnormal melanocyte morphology J:102101
abnormal retina pigment epithelium morphology J:33910
abnormal retina pigmentation J:33910
abnormal rod electrophysiology J:33910
absent coat pigmentation J:14091, J:102101
absent retina cone cells J:33910
absent retina rod cells J:33910
diluted coat color J:14091
fetal growth retardation J:33910
retina detachment J:33910
retina photoreceptor degeneration J:33910
variable depigmentation J:102101
white spotting J:14091
Mitfmi-vit/Mitfmi-vit
C57BL/6J-Mitfmi-vit/J 		abnormal iris pigmentation J:141035
diluted coat color J:100658
MitfMi-wh/Mitf+
involves: C57BL * DBA 		abnormal foot pigmentation J:13058
abnormal iris pigmentation J:125080
decreased eye pigmentation J:13058
decreased tail pigmentation J:13058
diluted coat color J:13058, J:125080
white spotting J:125080
MitfMi-wh/Mitfmi-sp
B6.Cg-MitfMi-wh/Mitfmi-sp/J 		abnormal coat/hair pigmentation J:12946, J:35685
abnormal foot pigmentation J:12946
abnormal hair shaft melanin granule morphology J:12946
decreased ear pigmentation J:12946
decreased tail pigmentation J:12946
diluted coat color J:12946
hypopigmentation J:12946
white spotting J:12946
yellow coat color J:12946
MitfMi-wh/MitfMi-wh
B6.Cg-MitfMi-wh 		abnormal optic choroid morphology J:5046
abnormal optic cup morphology J:5046
abnormal optic fissure closure J:5046
abnormal optic stalk morphology J:5046
abnormal posterior eye segment morphology J:5046
abnormal retina neuronal layer morphology J:5046
abnormal retina pigment epithelium morphology J:5046
abnormal retina pigmentation J:5046
decreased bleeding time J:7327
microphthalmia J:5046
normal skeleton phenotype J:5046
MitfMi-wh/MitfMi-wh
involves: C57BL * C57BL/6J * DBA 		absent coat pigmentation J:89821
decreased eye pigmentation J:89821
microphthalmia J:89821
normal skeleton phenotype J:89821
MitfMi-wh/MitfMi-wh
involves: C57BL * DBA 		abnormal cochlea morphology J:125080
abnormal cochlear hair cell morphology J:125080
abnormal stria vascularis morphology J:125080
abnormal vestibular saccule morphology J:125080
absent coat pigmentation J:13058, J:125080
decreased body size J:13058
decreased eye pigmentation J:125080
decreased litter size J:13058
microphthalmia J:13058, J:125080
ocular albinism J:13058
reduced fertility J:125080
MitfMi-wh/Mitfmi-x
involves: NZB/Mac 		abnormal eyelid morphology J:83501
microphthalmia J:83501
MitfMi-ws/Mitf+
involves: C57BL/6 		abnormal coat/hair pigmentation J:13417
belly spot J:13417
white spotting J:13417
MitfMi-ws/MitfMi-ws
involves: C57BL/6 		abnormal coat/hair pigmentation J:13417
abnormal eye development J:13417
abnormal eye morphology J:13417
abnormal eye pigmentation J:13417
abnormal eye size J:13417
absent coat pigmentation J:13417
decreased eye pigmentation J:13417
microphthalmia J:13417
Mitfmi-x39/Mitf+
involves: 102 * C3H 		belly spot J:62098
decreased eye pigmentation J:62098
Mitfmi-x39/Mitfmi-x39
involves: 102 * C3H 		absent coat pigmentation J:62098
irregular coat pigmentation J:62098
microphthalmia J:62098
Mitfmi-x/Mitfmi-x
involves: NZB/Mac 		abnormal coat/hair pigmentation J:83501
abnormal eye pigmentation J:83501
MitfMi/Mitf+
Not Specified 		abnormal coat/hair pigmentation J:125080
abnormal cochlea morphology J:125080
abnormal cochlear hair cell morphology J:125080
abnormal iris stromal pigmentation J:30758
abnormal stria vascularis morphology J:125080
abnormal vestibular saccule morphology J:125080
belly spot J:30758, J:125080
decreased eye pigmentation J:125080
head spot J:30758, J:125080
white spotting J:30758, J:125080
MitfMi/MitfMi-J
involves: C3HeB/Fe * C57BL/6J * C57BL/10J 		absent coat pigmentation J:78801
absent eye pigmentation J:78801
microphthalmia J:78801
MitfMi/Mitfmi-sp
B6.Cg-MitfMi/Mitfmi-sp 		absent coat pigmentation J:12946
absent skin pigmentation J:12946
decreased eye pigmentation J:12946
MitfMi/Mitfmi-sp
involves: C57BL/6J 		decreased eye pigmentation J:12946
hypopigmentation J:12946, J:35685
MitfMi/MitfMi
B6.Cg-MitfMi 		abnormal mast cell physiology J:53161
decreased serotonin level J:53161
MitfMi/MitfMi
involves: C57BL/6J 		abnormal osteoclast morphology J:89821
absent coat pigmentation J:89821
decreased body size J:89821
failure of tooth eruption J:89821
microphthalmia J:89821
osteopetrosis J:89821
postnatal lethality J:89821
MitfMi/MitfMi
Not Specified 		abnormal ciliary body morphology J:5046
abnormal cochlea morphology J:125080
abnormal cochlear hair cell morphology J:125080
abnormal eye development J:5046
abnormal optic choroid morphology J:5046
abnormal optic cup morphology J:5046
abnormal optic stalk morphology J:5046
abnormal osteoclast morphology J:5046
abnormal posterior eye segment morphology J:5046
abnormal retina neuronal layer morphology J:5046
abnormal retina pigment epithelium morphology J:5046
abnormal retina pigmentation J:5046
abnormal scala media morphology J:125080
abnormal skeleton morphology J:125080
abnormal stria vascularis morphology J:125080
abnormal vestibular saccule morphology J:125080
absent coat pigmentation J:30758, J:125080
absent optic nerve J:5046
coloboma J:5046
decreased eye pigmentation J:30758
decreased mast cell number J:6889
decreased survivor rate J:125080
eyelids fail to open J:125080
failure of tooth eruption J:30758
increased osteoclast cell number J:5046
microphthalmia J:5046, J:30758, J:125080
osteopetrosis J:30758
postnatal lethality J:30758
MitfMi/Mitftm1Arnh
involves: 129S1/Sv * C57BL/6 		absent coat pigmentation J:130168
normal vision/eye phenotype J:130168
MitfRorp/Mitf+
involves: BALB/cAnN * C3H/HeN 		abnormal coat/hair pigmentation J:75964
abnormal retina morphology J:75964
decreased ear pigmentation J:75964
decreased tail pigmentation J:75964
diluted coat color J:75964
MitfRorp/MitfRorp
involves: BALB/cAnN * C3H/HeN 		abnormal coat/hair pigmentation J:75964
abnormal iris pigmentation J:75964
abnormal retina morphology J:75964
absent coat pigmentation J:75964
coloboma J:75964
mydriasis J:75964
Mitftm1.1Arnh/Mitftm1.1Arnh
involves: 129S1/Sv * C3H/He * C57BL/6 		variegated coat color J:130168
Mitftm1Arnh/Mitftm1Arnh
involves: 129S1/Sv * C57BL/6 		absent coat pigmentation J:130168
irregular coat pigmentation J:130168
normal vision/eye phenotype J:130168
Mitftm3.1Arnh/Mitftm3.1Arnh
involves: 129S6/SvEvTac * C57BL/6N 		no abnormal phenotype detected J:188155
Mitftm4.1Arnh/MitfMi-wh
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL * C57BL/6N * DBA 		diluted coat color J:182722
white spotting J:182722
Mitftm4.1Arnh/Mitftm4.1Arnh
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6N 		normal pigmentation phenotype J:182722
Mitftm4Arnh/Mitfmi-vga9
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA 		absent coat pigmentation J:182722
Mitftm4Arnh/MitfMi-wh
involves: 129S6/SvEvTac * C57BL * C57BL/6N * DBA 		diluted coat color J:182722
white spotting J:182722
Mitftm4Arnh/MitfMi
involves: 129S6/SvEvTac * C57BL/6N 		absent coat pigmentation J:182722
Mitftm4Arnh/Mitftm4Arnh
involves: 129S6/SvEvTac * C57BL/6N 		belly spot J:182722
normal vision/eye phenotype J:182722
Mitftm5.1Arnh/MitfMi-wh
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL * C57BL/6N * DBA 		belly spot J:182722
darkened coat color J:182722
Mitftm5.1Arnh/Mitftm5.1Arnh
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6N 		normal pigmentation phenotype J:182722
Mitftm5Arnh/Mitfmi-vga9
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA 		belly spot J:182722
Mitftm5Arnh/MitfMi-wh
involves: 129S6/SvEvTac * C57BL * C57BL/6N * DBA 		diluted coat color J:182722
white spotting J:182722
Mitftm5Arnh/MitfMi
involves: 129S6/SvEvTac * C57BL/6N 		absent coat pigmentation J:182722
Mitftm5Arnh/Mitftm5Arnh
involves: 129S6/SvEvTac * C57BL/6N 		normal pigmentation phenotype J:182722
normal vision/eye phenotype J:182722
Mitftm6.1Arnh/MitfMi-wh
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL * C57BL/6N * DBA 		darkened coat color J:182722
Mitftm6.1Arnh/Mitftm6.1Arnh
involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6N 		normal pigmentation phenotype J:182722
Mitftm6Arnh/Mitfmi-vga9
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA 		irregular coat pigmentation J:182722
Mitftm6Arnh/MitfMi-wh
involves: 129S6/SvEvTac * C57BL * C57BL/6N * DBA 		diluted coat color J:182722
white spotting J:182722
Mitftm6Arnh/MitfMi
involves: 129S6/SvEvTac * C57BL/6N 		absent coat pigmentation J:182722
Mitftm6Arnh/Mitftm6Arnh
involves: 129S6/SvEvTac * C57BL/6N 		belly spot J:182722
normal vision/eye phenotype J:182722
Mitftm7.1Arnh/MitfMi-wh
involves: 129S6/SvEvTac * C57BL * C57BL/6N * DBA 		belly spot J:182722
darkened coat color J:182722
Mitftm7Arnh/Mitfmi-vga9
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * CBA 		irregular coat pigmentation J:182722
Mitftm7Arnh/MitfMi-wh
involves: 129S6/SvEvTac * C57BL * C57BL/6N * DBA 		diluted coat color J:182722
white spotting J:182722
Mitftm7Arnh/MitfMi
involves: 129S6/SvEvTac * C57BL/6N 		absent coat pigmentation J:182722
Mitftm7Arnh/Mitftm7Arnh
involves: 129S6/SvEvTac * C57BL/6N 		belly spot J:182722
normal vision/eye phenotype J:182722
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12/17/2024
MGI 6.24 		The Jackson Laboratory