Homo sapiens Gene: FMNL3
Summary
InnateDB Gene IDBG-31836.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FMNL3
Gene Name formin-like 3
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000161791
Encoded Proteins
formin-like 3
formin-like 3
formin-like 3
formin-like 3
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene contains a formin homology 2 domain and has high sequence identity to the mouse Wbp3 protein. Two alternative transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 12:49636499-49708165
Strand Reverse strand
Band q13.12
Transcripts
ENST00000335154 ENSP00000335655
ENST00000352151 ENSP00000344311
ENST00000550668
ENST00000550488 ENSP00000447479
ENST00000549137
ENST00000550970
ENST00000550424 ENSP00000448939
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 9 experimentally validated interaction(s) in this database.
Experimentally validated
Total 9 [view]
Protein-Protein 9 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003779 actin binding
GO:0005488 binding
GO:0005515 protein binding
GO:0017048 Rho GTPase binding
GO:0032794 GTPase activating protein binding
Biological Process
GO:0007010 cytoskeleton organization
GO:0008360 regulation of cell shape
GO:0016043 cellular component organization
GO:0016477 cell migration
GO:0030036 actin cytoskeleton organization
Cellular Component
GO:0005737 cytoplasm
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
Non-SSD Ortholog
Possible paralog/unusual divergence/ gene prediction error
Not yet available
Non-SSD Ortholog
Possible paralog/unusual divergence/ gene prediction error
Cross-References
SwissProt
TrEMBL F8VYL1
UniProt Splice Variant
Entrez Gene 91010
UniGene Hs.179838 Hs.33104 Hs.657959 Hs.708422
RefSeq NM_175736 NM_198900 XM_005269218 XM_005269219
HUGO HGNC:23698
OMIM
CCDS CCDS41780 CCDS44874
HPRD 17007
IMGT
EMBL AC020612
GenPept
RNA Seq Atlas 91010