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EPB41L1

erythrocyte membrane protein band 4.1 like 1

HCNC Approved Symbol
EPB41L1 (HGNC:3378)
Genomic Coordinates
20:36,091,414 - 36,232,799 (20q11.23)
Synonyms
KIAA0338, 4.1N
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
?Intellectual developmental disorder, autosomal dominant 11
614257AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the EPB41L1 gene.

Frequently observed phenotypes

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

No Results