Symbol Name ID

Mitf microphthalmia-associated transcription factor MGI:104554

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8 matching Alleles (1 Gene/Marker represented)

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                                          Allele Symbol
Name                                            Chr    Synonyms            Category                                                                                    Phenotypic Classes                                                                                                                                                      Human Diseases                                                                         

MitfMi
microphthalmia-associated transcription factor; microphthalmia
                                   6    m, mi         Not Specified             craniofacial, growth/size, hearing/vestibular/ear, hematopoietic, homeostasis, immune, integument, mortality/aging, nervous system, pigmentation, skeleton, vision/eye  Albinism, Ocular, with Sensorineural Deafness 103470; Tietz Syndrome 103500; Waardenburg Syndrome, Type 2A; WS2A 193510                                          

MitfMi-Crc
microphthalmia-associated transcription factor; microphthalmia MRC Clinical Research Centre  6    miCrc         Spontaneous               craniofacial, integument, limbs/digits/tail, pigmentation, reproductive, skeleton, vision/eye                                                                           Albinism, Ocular, with Sensorineural Deafness 103470; Tietz Syndrome 103500; Waardenburg Syndrome, Type 1; WS1 193500; Waardenburg Syndrome, Type 2A; WS2A 193510

Mitfmi-enu122
microphthalmia-associated transcription factor; microphthalmia enu 122
                    6    ENU-122       Chemically induced (ENU)  integument, limbs/digits/tail, pigmentation, vision/eye                                                                                                                 Albinism, Ocular, with Sensorineural Deafness 103470; Tietz Syndrome 103500; Waardenburg Syndrome, Type 2A; WS2A 193510                                          

Mitfmi-ew
microphthalmia-associated transcription factor; eyeless white                                 6    miew          Spontaneous               integument, pigmentation, skeleton, vision/eye                                                                                                                          Camurati-Engelmann Disease; CAEND 131300                                                                                                                         

MitfMi-H
microphthalmia-associated transcription factor; microphthalmia Harwell                         6    GENA 163      Chemically induced (ENU)  craniofacial, hearing/vestibular/ear, integument, limbs/digits/tail, pigmentation, vision/eye                                                                           Albinism, Ocular, with Sensorineural Deafness 103470; Tietz Syndrome 103500; Waardenburg Syndrome, Type 2A; WS2A 193510                                          

MitfMi-wh
microphthalmia-associated transcription factor; white
                                         6    mitfwh, Miwh  Spontaneous               craniofacial, growth/size, hearing/vestibular/ear, homeostasis, integument, limbs/digits/tail, nervous system, pigmentation, reproductive, vision/eye                   Albinism, Ocular, with Sensorineural Deafness 103470; Tietz Syndrome 103500; Waardenburg Syndrome, Type 2A; WS2A 193510                                          

Mitfmi-x
microphthalmia-associated transcription factor; microphthalmia x                               6    mix           Spontaneous               integument, pigmentation, vision/eye                                                                                                                                    Albinism, Ocular, with Sensorineural Deafness 103470; Tietz Syndrome 103500; Waardenburg Syndrome, Type 2A; WS2A 193510                                          

MitfRorp
microphthalmia-associated transcription factor; retinal orange patches                         6    GENA 366      Chemically induced (ENU)  craniofacial, hearing/vestibular/ear, integument, limbs/digits/tail, pigmentation, vision/eye                                                                           Albinism, Ocular, with Sensorineural Deafness 103470; Tietz Syndrome 103500; Waardenburg Syndrome, Type 2A; WS2A 193510