View FGF3 gene homepage

General information
Gene symbol FGF3
Gene name fibroblast growth factor 3
Chromosome 11
Chromosomal band q13
Imprinted Unknown
Genomic reference NG_009016.1
Transcript reference NM_005247.2
Associated with diseases deafness, congenital, inner ear agenesis, microtia, and microdontia (deafness with LAMM), Otodental dysplasia chromsome deletion syndrome
Citation reference(s) -
Curators (1) LOVD-team, but with Curator vacancy
Total number of public variants reported 0
Unique public DNA variants reported 0
Individuals with public variants 0
Hidden variants 0
Date created May 03, 2013

Links to other resources
HGNC 3681
Entrez Gene 2248
PubMed articles FGF3
OMIM - Gene 164950
OMIM - Diseases deafness, congenital, inner ear agenesis, microtia, and microdontia (deafness with LAMM)


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00007908 11 fibroblast growth factor 3 NM_005247.2 NP_005238.1 0