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CLDN17

claudin 17

HCNC Approved Symbol
CLDN17 (HGNC:2038)
Genomic Coordinates
21:30,165,565 - 30,166,805 (21q21.3)
Synonyms
MGC126552, MGC126554
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

CLDN17 - Gene browser | 3billion