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FBXL3

F-box and leucine rich repeat protein 3

HCNC Approved Symbol
FBXL3 (HGNC:13599)
Genomic Coordinates
13:77,005,260 - 77,027,159 (13q22.3)
Synonyms
FBL3, FBL3A, FBXL3A
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Intellectual developmental disorder with short stature, facial anomalies, and speech defects
606220AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the FBXL3 gene.

Frequently observed phenotypes

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

No Results