FMN1 (Entrez ID: 342184)

Entrez Gene ID	342184
Official Gene Symbol	FMN1 (GeneCards)
Full name	formin 1
Location	15q13.3
Other ids	Vega : OTTHUMG00000172201 MIM : 136535 HGNC : HGNC:3768 Ensembl : ENSG00000248905
Other names	LD, FMN
Summary	This gene belongs to the formin homology family and encodes a protein that has a role in the formation of adherens junction and the polymerization of linear actin cables. The homologous gene in mouse is associated with limb deformity. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2015]

Variants

Found 8 variants in this database.

Variant ID	Entrez Gene ID	Gene	Chromsome	Start	End	Disease	Method
18735	342184	FMN1	15	33206682	33206682	Asymptomatic	HiSeq X Ten
18772	342184	FMN1	15	33436013	33436013	Asymptomatic	HiSeq X Ten
18891	342184	FMN1	15	33490015	33490015	Asymptomatic	HiSeq X Ten
18896	342184	FMN1	15	33335265	33335265	Asymptomatic	HiSeq X Ten
18985	342184	FMN1	15	33105719	33105719	Asymptomatic	HiSeq X Ten
19039	342184	FMN1	15	33210572	33210572	Asymptomatic	HiSeq X Ten
19260	342184	FMN1	15	33283008	33283008	Cockayne syndrome	HiSeq X Ten
28109	342184	FMN1	15	33473846	33473846	Asymptomatic	HiSeq X Ten Single cell Sequencing Cell cloning