Gene: DIAPH3

Alternate names for this Gene: AN|AUNA1|DIA2|DRF3|NSDAN|diap3|mDia2

Gene Summary: This gene encodes a member of the diaphanous subfamily of the formin family. Members of this family are involved in actin remodeling and regulate cell movement and adhesion. Mutations in this gene are associated with autosomal dominant auditory neuropathy 1. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene is located in Chromosome: 13

Location in Chromosome : 13q21.2

Description of this Gene: diaphanous related formin 3

Type of Gene: protein-coding

Gene: DIAPH3-AS1

Alternate names for this Gene: -

Gene Summary:

Gene is located in Chromosome: 13

Location in Chromosome : 13q21.2

Description of this Gene: DIAPH3 antisense RNA 1

Type of Gene: ncRNA

rs17057556 in DIAPH3;DIAPH3-AS1 gene and Leukemia, Myelocytic, Acute PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.