Homo sapiens Protein: FCHSD2
Summary
InnateDB Protein IDBP-63687.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FCHSD2
Protein Name FCH and double SH3 domains 2
Synonyms NWK; SH3MD3;
Species Homo sapiens
Ensembl Protein ENSP00000308978
InnateDB Gene IDBG-63685 (FCHSD2)
Protein Structure
UniProt Annotation
Function
Subcellular Localization
Disease Associations
Tissue Specificity Liver, brain, heart, placenta, skeletal muscle, pancreas, lung and kidney. {ECO:0000269PubMed:14627983}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 27 experimentally validated interaction(s) in this database.
Experimentally validated
Total 27 [view]
Protein-Protein 26 [view]
Protein-DNA 0
Protein-RNA 1 [view]
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
Biological Process
Cellular Component
Protein Structure and Domains
PDB ID
InterPro IPR001060 FCH domain
IPR001452 SH3 domain
IPR011511 Variant SH3 domain
PFAM PF00611
PF00018
PF14604
PF07653
PRINTS PR00452
PIRSF
SMART SM00055
SM00326
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt O94868
PhosphoSite PhosphoSite-O94868
TrEMBL A0A024R5H2
UniProt Splice Variant
Entrez Gene 9873
UniGene Hs.743346
RefSeq
HUGO HGNC:29114
OMIM
CCDS
HPRD 13321
IMGT
EMBL AB018312 AK297928 AL133567 AP002381 AP002455 AP004241 BC010394 BC017751 CH471076
GenPept AAH10394 AAH17751 BAA34489 BAG60245 CAB63720 EAW74880 EAW74881