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FLNB

filamin B

HCNC Approved Symbol
FLNB (HGNC:3755)
Genomic Coordinates
3:58,008,422 - 58,172,251 (3p14.3)
Synonyms
TAP, TABP, ABP-278, FH1, FLN1L, LRS1
Disease Associations
This gene is associated with the following 5 diseases in OMIM.

Diagnosed Cases

15Patients

In total, 15 patients were diagnosed with a variant in the FLNB gene.

Frequently observed phenotypes

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

Epicanthus
 
2 (13.3%)
Low birth weight
 
2 (13.3%)
Postnatal growth failure
 
2 (13.3%)
Progressive skeletal dysplasia
 
2 (13.3%)
Small for gestational age infant
 
2 (13.3%)
FLNB - Gene browser | 3billion