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ACTB

actin beta

HCNC Approved Symbol
ACTB (HGNC:132)
Genomic Coordinates
7:5,527,148 - 5,530,601 (7p22.1)
Synonyms
Disease Associations
This gene is associated with the following 5 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Baraitser-Winter syndrome 1
243310AD
Becker nevus, syndromic or isolated, somatic mosaic
604919-
Congenital smooth muscle hamartoma with or without hemihypertrophy, somatic mosaic
620479-
Dystonia-deafness syndrome 1
607371AD
Thrombocytopenia 8, with dysmorphic features and developmental delay
620475AD

Diagnosed Cases

23Patients

In total, 23 patients were diagnosed with a variant in the ACTB gene.

Frequently observed phenotypes

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

Hypertelorism
 6 (26.1%)
Short neck
 6 (26.1%)
Global developmental delay
 5 (21.7%)
Failure to thrive
 4 (17.4%)
Microcephaly
 4 (17.4%)