Homo sapiens Protein: C4orf26
Summary
InnateDB Protein IDBP-24644.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C4orf26
Protein Name chromosome 4 open reading frame 26
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000311307
InnateDB Gene IDBG-24642 (C4orf26)
Protein Structure
UniProt Annotation
Function Might promote nucleation of hydroxyapatite. {ECO:0000269PubMed:22901946}.
Subcellular Localization Secreted {ECO:0000305}.
Disease Associations Amelogenesis imperfecta, hypomaturation type, 2A4 (AI2A4) [MIM:614832]: A defect of enamel formation. The disorder involves both primary and secondary dentitions. The teeth have a shiny agar jelly appearance and the enamel is softer than normal. Brown pigment is present in middle layers of enamel. {ECO:0000269PubMed:22901946}. Note=The disease is caused by mutations affecting the gene represented in this entry.
Tissue Specificity Highly expressed in placenta. {ECO:0000269PubMed:22901946}.
Comments
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
Cellular Component
GO:0005576 extracellular region
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q17RF5
PhosphoSite PhosphoSite-Q17RF5
TrEMBL
UniProt Splice Variant
Entrez Gene 152816
UniGene Hs.24510
RefSeq NP_848592
HUGO HGNC:26300
OMIM 614829
CCDS CCDS3569
HPRD 08040
IMGT
EMBL AC096759 AK074237 AK172776 AK300227 BC117342 CH471057
GenPept AAI17343 BAB85027 BAD18758 BAG61995 EAX05738