Bos taurus Gene: FAM20C
Summary
InnateDB Gene IDBG-641524.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM20C
Gene Name Uncharacterized protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000003607
Encoded Proteins
family with sequence similarity 20, member C
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000177706:
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 25:42694393-42728472
Strand Reverse strand
Band
Transcripts
ENSBTAT00000004699 ENSBTAP00000004699
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
Predicted by orthology
Total 5 [view]
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: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
Homo sapiens
Mus musculus
Gene ID
Gene Order
Cross-References
SwissProt
TrEMBL F1MXQ3
UniProt Splice Variant
Entrez Gene 534672
UniGene
RefSeq XM_002698175 XM_614520
HUGO HGNC:22140
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02058442 DAAA02058443
GenPept
RNA Seq Atlas 534672