ODAPH
Odontogenesis associated phosphoprotein
Also known as: AI2A4, C4orf26, FLJ23657, ODAPH_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q17RF5
- Gene
- ODAPH
- Ensembl
- ENSG00000174792
- Chromosome
- 4
- Canonical length
- 130 aa
- Protein class
- Disease related genes, Human disease related genes, Predicted secreted proteins
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
Dental enamel forms the outer cap of teeth and is the hardest substance found in vertebrates. This gene is thought to encode an extracellular matrix acidic phosphoprotein that has a function in enamel mineralization during amelogenesis. Mutations in this gene are associated with recessive hypomineralized amelogenesis imperfecta. [provided by RefSeq, Oct 2012]
Canonical amino-acid sequenceUniProt
130 residues, UniProt reviewed canonical sequence.
>Q17RF5|ODAPH
1 MARRHCFSYW LLVCWLVVTV AEGQEEVFTP PGDSQNNADA TDCQIFTLTP PPAPRSPVTR
61 AQPITKTPRC PFHFFPRRPR IHFRFPNRPF VPSRCNHRFP FQPFYWPHRY LTYRYFPRRR
121 LQRGSSSEESLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ODAPH can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.69
- Highest tissue expression
- 5.5 nTPM
Expression across tissuesHPA
Tissue
- placenta: 5.5 nTPM
- spinal cord: 1.1 nTPM
- midbrain: 1 nTPM
- skeletal muscle: 0.8 nTPM
- hippocampal formation: 0.7 nTPM
- amygdala: 0.6 nTPM
Single-cell type
- syncytiotrophoblasts: 35 nCPM
- extravillous trophoblasts: 14 nCPM
- plasma cells: 9.3 nCPM
- migrating cytotrophoblasts: 7.2 nCPM
- late primary spermatocytes: 4.1 nCPM
- early spermatids: 3.2 nCPM
Immune cell
- basophil: 11 nTPM
- MAIT T-cell: 0.3 nTPM
- naive B-cell: 0.3 nTPM
- neutrophil: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- intermediate monocyte: 0.1 nTPM
Brain region
- white matter: 3.4 nTPM
- cerebral cortex: 2.5 nTPM
- pons: 2.4 nTPM
- cerebellum: 2.2 nTPM
- medulla oblongata: 2.1 nTPM
- midbrain: 2 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about ODAPH.
Disease | AllUniProt
Conditions ODAPH is implicated in, by any mechanism.
- Amelogenesis imperfecta, hypomaturation type, 2A4 (AI2A4) MIM:614832
Disease | GeneticClinVar
7 pathogenic / likely-pathogenic of 24 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Amelogenesis imperfecta hypomaturation type 2A4
- ODAPH-related disorder
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.67
- gnomAD pLI
- 0.05
- DepMap mean gene effect
- 0.11
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Odontogenesis associated phosphoprotein
- Odontogenesis associated phosphoprotein
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ODAPH as an antibody target. Whether an autoantibody or antibody against ODAPH could matter depends on whether native ODAPH is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ODAPH is annotated as secreted, so native ODAPH circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label ODAPH as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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