SLC5A7

solute carrier family 5 member 7

HCNC Approved Symbol

SLC5A7 (HGNC:14025)

Genomic Coordinates

2:107,986,524 - 108,013,994 (2q12.3)

Synonyms

hCHT, CHT1, ChT

Disease Associations

This gene is associated with the following 2 diseases in OMIM.

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Disease NameOMIM IDInheritance

Myasthenic syndrome, congenital, 20, presynaptic

617143AR

Neuronopathy, distal hereditary motor, autosomal dominant 7

158580AD