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KRT86

keratin 86

HCNC Approved Symbol
KRT86 (HGNC:6463)
Genomic Coordinates
12:52,274,645 - 52,309,163 (12q13)
Synonyms
MNX, Hb6, KRTHB6
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the KRT86 gene.

Frequently observed phenotypes

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

Hypotrichosis of eyebrow
 1 (50.0%)
Hypotrichosis of eyelashes
 1 (50.0%)
Hypotrichosis of lower eyelashes
 1 (50.0%)
Hypotrichosis of upper eyelashes
 1 (50.0%)
Hypotrichosis, generalized
 1 (50.0%)
KRT86 - Gene browser | 3billion