Homo sapiens Gene: FAM20C
Summary
InnateDB Gene IDBG-6057.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM20C
Gene Name family with sequence similarity 20, member C
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000177706
Encoded Proteins
family with sequence similarity 20, member C
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the family with sequence similarity 20 (FAM20) family of secreted proteins. A similar gene in mice encodes a protein that plays a role in dentin mineralization, and mutations in the human gene are associated with the autosomal recessive disorder Raine syndrome. [provided by RefSeq, Nov 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 7:192969-260745
Strand Forward strand
Band p22.3
Transcripts
ENST00000313766 ENSP00000322323
ENST00000477004
ENST00000471328
ENST00000515795
ENST00000512382
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 15 experimentally validated interaction(s) in this database.
Experimentally validated
Total 15 [view]
Protein-Protein 15 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0004674 protein serine/threonine kinase activity
GO:0005509 calcium ion binding
Biological Process
GO:0001501 skeletal system development
GO:0006468 protein phosphorylation
GO:0030501 positive regulation of bone mineralization
GO:0036179 osteoclast maturation
GO:0040036 regulation of fibroblast growth factor receptor signaling pathway
GO:0045669 positive regulation of osteoblast differentiation
GO:0051174 regulation of phosphorus metabolic process
GO:0070166 enamel mineralization
GO:0071895 odontoblast differentiation
GO:0097187 dentinogenesis
Cellular Component
GO:0005615 extracellular space
GO:0005794 Golgi apparatus
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene
RefSeq NM_020223 XM_005249814
HUGO
OMIM
CCDS CCDS47522
HPRD 13298
IMGT
EMBL
GenPept
RNA Seq Atlas