Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

Hereditary FSGS type 8

Hereditary FSGS type 8 is an autosomal dominant disorder caused by mutations of the ANLN gene.

Systematic

Focal, segmental glomerulosclerosis (FSGS)
ALG13
ARHGAP24
CLU
Hereditary FSGS type 1
Hereditary FSGS type 2
Hereditary FSGS type 3
Hereditary FSGS type 4
Hereditary FSGS type 5
Hereditary FSGS type 6
Hereditary FSGS type 7
Hereditary FSGS type 8
ANLN
Hereditary FSGS type 9
ITGA9
LAMA5
NXF5

References:

1.

Gbadegesin RA et al. (2014) Mutations in the gene that encodes the F-actin binding protein anillin cause FSGS.

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Update: Nov. 3, 2022
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