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Phenotypic Alleles
Query Results -- Summary
 Symbol
Name
ID
Mitf
microphthalmia-associated transcription factor
MGI:104554

8 matching Alleles (1 Gene/Marker represented)
                                          Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases MitfMi
microphthalmia-associated transcription factor; microphthalmia
images 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
images 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 Gena163, 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
images 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 Gena336, GENA 336 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

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory