MITF / melanogenesis associated transcription factor

  
type: protein-coding
synonyms: CMM8|COMMAD|MI|WS2|WS2A|bHLHe32
Omim:
156845
Cytogenetic location:
3p13
Genetic associations:

Tietz syndrome

(monogenic disease that is characterized by congenital profound bilateral sensorineural hearing loss and generalized albino-like hypopigmentation of skin, eyes and hair that has material basis in mutation in the MITF gene on chromosome 3p13)
Waardenburg syndrome type 2A

(Waardenburg syndrome Type 2 caused by mutations in the MITF gene)

MITF interactions network
Curated interactions:
Last networks with gene MITF:
network_1496896332 08 June 2017 11:32:51 by guest (autosave)
1498493016 26 June 2017 21:07:00 by Sasha Fokin (autosave)
network_1498859849 01 July 2017 02:58:33 by Rhizoman1 (autosave)
network_1506955926 02 October 2017 21:12:39 by guest (autosave)
network_1509020359 26 October 2017 17:30:05 by guest (autosave)
network_1511081245 19 November 2017 13:03:10 by guest (autosave)
network_1511086589 19 November 2017 14:17:49 by guest (autosave)
network_1511095040 19 November 2017 16:39:12 by Sasha Fokin (autosave)
network_1511249624 21 November 2017 11:42:38 by guest (autosave)
Aging_serum_6_mirna_siganture 21 November 2017 11:44:14 by guest