KRT2 - Gene browser | 3billion

KRT2

KRT2

keratin 2

HCNC Approved Symbol: KRT2 (HGNC:6439)
Genomic Coordinates: 12:52,644,558 - 52,652,211 (12q13.13)
Synonyms: KRTE, KRT2A
Disease Associations: This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

1Patient

In total, 1 patient was diagnosed with a variant in the KRT2 gene.

Frequently observed phenotypes(Top 5 only)

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

01
Patient count

Congenital bullous ichthyosiform erythroderma: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Epidermolytic hyperkeratosis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)
Ichthyosis: 1 (100.0%)
Patient Count: 1 (100.0%)
% of total patients presenting each phenotype is shown in parentheses.
1 (100.0%)

Last updated: 2024-06-30

KRT2 - Gene browser | 3billion