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BHLHE41

basic helix-loop-helix family member e41

HCNC Approved Symbol
BHLHE41 (HGNC:16617)
Genomic Coordinates
12:26,120,030 - 26,125,037 (12p12.1)
Synonyms
DEC2, SHARP-1, SHARP1, BHLHB3
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
[Short sleep, familial natural, 1]
612975AD

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the BHLHE41 gene.

Frequently observed phenotypes

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

No Results