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
|
Excel File
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