OSR1
Protein odd-skipped-related 1
Also known as: ODD, OSR1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8TAX0
- Gene
- OSR1
- Ensembl
- ENSG00000143867
- Chromosome
- 2
- Canonical length
- 266 aa
- Protein class
- Predicted intracellular proteins, Transcription factors
OverviewNCBI Gene
Enables sequence-specific double-stranded DNA binding activity. Involved in negative regulation of transporter activity; positive regulation of gastrulation; and pronephros development. Located in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
266 residues, UniProt reviewed canonical sequence.
>Q8TAX0|OSR1
1 MGSKTLPAPV PIHPSLQLTN YSFLQAVNGL PTVPSDHLPN LYGFSALHAV HLHQWTLGYP
61 AMHLPRSSFS KVPGTVSSLV DARFQLPAFP WFPHVIQPKP EITAGGSVPA LKTKPRFDFA
121 NLALAATQED PAKLGRGEGP GSPAGGLGAL LDVTKLSPEK KPTRGRLPSK TKKEFVCKFC
181 GRHFTKSYNL LIHERTHTDE RPYTCDICHK AFRRQDHLRD HRYIHSKEKP FKCQECGKGF
241 CQSRTLAVHK TLHSQVKELK TSKIKCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against OSR1 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.62
- Highest tissue expression
- 100 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 100 nTPM
- urinary bladder: 70 nTPM
- adipose tissue: 37 nTPM
- salivary gland: 30 nTPM
- cervix: 23 nTPM
- colon: 23 nTPM
Single-cell type
- leydig cells: 118 nCPM
- peritubular myoid cells: 45 nCPM
- mesothelial cells: 40 nCPM
- salivary myoepithelial cells: 35 nCPM
- fibroblasts: 30 nCPM
- epicardial cells: 21 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- thalamus: 8 nTPM
- choroid plexus: 4.3 nTPM
- hippocampal formation: 3.9 nTPM
- cerebral cortex: 3.7 nTPM
- basal ganglia: 1.6 nTPM
- medulla oblongata: 1.1 nTPM
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)
- 0.46
- gnomAD pLI
- 0.86
- gnomAD missense Z
- 1.74
- DepMap mean gene effect
- 0.07
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation
- cell proliferation involved in kidney development
- cellular response to retinoic acid
- chondrocyte differentiation
- embryonic digit morphogenesis
- embryonic forelimb morphogenesis
- embryonic hindlimb morphogenesis
- embryonic skeletal joint development
- embryonic skeletal joint morphogenesis
- embryonic skeletal limb joint morphogenesis
- gonad development
- heart development
- mesonephric duct morphogenesis
- mesonephros development
- metanephric epithelium development
- metanephric glomerulus vasculature development
- metanephric mesenchymal cell differentiation
- metanephric mesenchyme development
- metanephric mesenchyme morphogenesis
- metanephric smooth muscle tissue development
- middle ear morphogenesis
- negative regulation of apoptotic process
- negative regulation of epithelial cell differentiation
- negative regulation of sodium ion transmembrane transport
- negative regulation of transcription by RNA polymerase II
- negative regulation of transmembrane transport
- odontogenesis
- pattern specification process
- positive regulation of bone mineralization
- positive regulation of epithelial cell proliferation
- positive regulation of gastrulation
- positive regulation of gene expression
- positive regulation of transcription by RNA polymerase II
- posterior mesonephric tubule development
- pronephros development
- roof of mouth development
- sodium ion transmembrane transport
- stem cell differentiation
- ureter urothelium development
- ureteric bud development
- urogenital system development
- intermediate mesoderm development
- mesangial cell development
- metanephric cap mesenchymal cell proliferation involved in metanephros development
- metanephric interstitial fibroblast development
- metanephric nephron tubule development
- negative regulation of nephron tubule epithelial cell differentiation
- pattern specification involved in metanephros development
- renal vesicle progenitor cell differentiation
- specification of anterior mesonephric tubule identity
- specification of posterior mesonephric tubule identity
Molecular functions
- DNA-binding transcription factor activity, RNA polymerase II-specific
- RNA polymerase II transcription regulatory region sequence-specific DNA binding
- sequence-specific double-stranded DNA binding
- transporter inhibitor activity
- zinc ion binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of OSR1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads OSR1 as an antibody target. Whether an autoantibody or antibody against OSR1 could matter depends on whether native OSR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
OSR1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label OSR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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