Homo sapiens Gene: FCHO2
Summary
InnateDB Gene IDBG-27912.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FCHO2
Gene Name FCH domain only 2
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000157107
Encoded Proteins
FCH domain only 2
FCH domain only 2
FCH domain only 2
FCH domain only 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary Currently no Entrez Summary Available. You might want to check the Summary Sections of the Orthologs.
Gene Information
Type Protein coding
Genomic Location Chromosome 5:72955981-73090522
Strand Forward strand
Band q13.2
Transcripts
ENST00000287761 ENSP00000287761
ENST00000430046 ENSP00000393776
ENST00000512348 ENSP00000427296
ENST00000507345 ENSP00000426842
ENST00000511264
ENST00000503302
ENST00000508431
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 10 [view]
Protein-Protein 10 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0001786 phosphatidylserine binding
GO:0005515 protein binding
GO:0005546 phosphatidylinositol-4,5-bisphosphate binding
GO:0035091 phosphatidylinositol binding
Biological Process
GO:0010324 membrane invagination
GO:0048268 clathrin coat assembly
GO:0072583 clathrin-mediated endocytosis
GO:0072659 protein localization to plasma membrane
Cellular Component
GO:0005886 plasma membrane
GO:0005905 coated pit
GO:0030136 clathrin-coated vesicle
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt Q0JRZ9
TrEMBL B4DEU7
UniProt Splice Variant
Entrez Gene 115548
UniGene Hs.165762 Hs.741336
RefSeq NM_138782 NM_001146032
HUGO HGNC:25180
OMIM 613438
CCDS CCDS47230 CCDS54868
HPRD 13319
IMGT
EMBL AC008972 AC020893 AC020942 AK291782 AK293796 AK295141 AL831971 BC014311 BC137070
GenPept AAH14311 AAI37071 BAF84471 BAG57208 BAG58162
RNA Seq Atlas 115548