ALKBH7

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Description

The ALKBH7 (alkB homolog 7) is a protein-coding gene located on chromosome 19.

ALKBH7 is also known as ABH7, SPATA11, UNQ6002.

Associated Diseases

• cancer
• glioblastoma
• hyperinsulinism due to HNF1A deficiency
• obesity due to melanocortin 4 receptor deficiency
• autosomal dominant hyperinsulinism due to SUR1 deficiency
• autosomal dominant hyperinsulinism due to Kir6.2 deficiency
• hyperinsulinism due to UCP2 deficiency
• familial partial lipodystrophy, Dunnigan type
• obesity due to prohormone convertase I deficiency
• obesity due to pro-opiomelanocortin deficiency
• CIDEC-related familial partial lipodystrophy
• LIPE-related familial partial lipodystrophy
• PPARG-related familial partial lipodystrophy
• familial partial lipodystrophy, Kobberling type
• AKT2-related familial partial lipodystrophy
• cerebellar degeneration