InnateDB Protein
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IDBP-24644.5
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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C4orf26
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Protein Name
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chromosome 4 open reading frame 26
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Synonyms
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000311307
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InnateDB Gene
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IDBG-24642 (C4orf26)
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Protein Structure
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Function |
Might promote nucleation of hydroxyapatite. {ECO:0000269PubMed:22901946}.
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Subcellular Localization |
Secreted {ECO:0000305}.
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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.
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Tissue Specificity |
Highly expressed in placenta. {ECO:0000269PubMed:22901946}.
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
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PFAM |
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PRINTS |
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
Q17RF5
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PhosphoSite |
PhosphoSite-Q17RF5
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TrEMBL |
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UniProt Splice Variant |
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Entrez Gene |
152816
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UniGene |
Hs.24510
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RefSeq |
NP_848592
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HUGO |
HGNC:26300
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OMIM |
614829
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CCDS |
CCDS3569
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HPRD |
08040
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IMGT |
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EMBL |
AC096759
AK074237
AK172776
AK300227
BC117342
CH471057
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GenPept |
AAI17343
BAB85027
BAD18758
BAG61995
EAX05738
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