TMEM50B

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Description

The TMEM50B (transmembrane protein 50B) is a protein-coding gene located on chromosome 21.

TMEM50B is also known as C21orf4, HCVP7TP3.

Associated Diseases

• corneal endothelial dystrophy
• megalocornea
• keratoconus
• keratoconus 1
• macular corneal dystrophy
• congenital stromal corneal dystrophy
• cornea plana 2
• congenital hereditary endothelial dystrophy of cornea
• EDICT syndrome
• Dravet syndrome