Homo sapiens Gene: FAM83H
Summary
InnateDB Gene IDBG-39015.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM83H
Gene Name family with sequence similarity 83, member H
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000180921
Encoded Proteins
family with sequence similarity 83, member H
family with sequence similarity 83, member H
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene plays an important role in the structural development and calcification of tooth enamel. Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3). [provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 8:143723933-143733801
Strand Reverse strand
Band q24.3
Transcripts
ENST00000388913 ENSP00000373565
ENST00000395103 ENSP00000378535
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 11 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 11 [view]
Protein-Protein 11 [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
Biological Process
GO:0031214 biomineral tissue development
Cellular Component
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q6ZRV2
TrEMBL F4ZCG5
UniProt Splice Variant
Entrez Gene 286077
UniGene Hs.645726 Hs.67776 Hs.713170
RefSeq NM_198488 XM_005250887 XM_005250888 XM_005250889 XM_005250890 XM_006725087 XM_006725088 XM_006725089 XM_006725090
HUGO HGNC:24797
OMIM 611927
CCDS CCDS6410
HPRD
IMGT
EMBL AC105219 AK127960 BC007264 BC033256 HM481257
GenPept AAH07264 AAH33256 AEB00836 BAC87207
RNA Seq Atlas 286077