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KREMEN1

kringle containing transmembrane protein 1

HCNC Approved Symbol
KREMEN1 (HGNC:17550)
Genomic Coordinates
22:29,073,035 - 29,168,333 (22q12.1)
Synonyms
KRM1, KREMEN
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Ectodermal dysplasia 13, hair/tooth type
617392AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the KREMEN1 gene.

Frequently observed phenotypes

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

No Results