Homo sapiens Gene: FAM20A
Summary
InnateDB Gene IDBG-65964.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM20A
Gene Name family with sequence similarity 20, member A
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000108950
Encoded Proteins
family with sequence similarity 20, member A
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identified. [provided by RefSeq, Aug 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 17:68535113-68601389
Strand Reverse strand
Band q24.2
Transcripts
ENST00000226094
ENST00000375556
ENST00000592554 ENSP00000468308
ENST00000590074 ENSP00000464910
ENST00000590873 ENSP00000467884
ENST00000592847
ENST00000619787 ENSP00000481085
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0044691 tooth eruption
GO:0055074 calcium ion homeostasis
GO:0070166 enamel mineralization
Cellular Component
GO:0005623 cell
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 Hs.678664
RefSeq NM_001243746 NM_017565 XM_006721958 XM_006721959 XM_006721960
HUGO
OMIM
CCDS CCDS11679
HPRD 13296
IMGT
EMBL
GenPept
RNA Seq Atlas