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KRT16

keratin 16

HCNC Approved Symbol
KRT16 (HGNC:6423)
Genomic Coordinates
17:41,609,778 - 41,612,767 (17q21.2)
Synonyms
NEPPK
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the KRT16 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Plantar hyperkeratosis
 1 (100.0%)
KRT16 - Gene browser | 3billion