OOSP4A
gene geneOn this page
Summary
OOSP4A (oocyte secreted protein family member 4A, HGNC:53904) is a protein-coding gene on chromosome 11q12.1, encoding Oocyte-secreted protein 4A (A0A2R8YFL7).
Predicted to be located in extracellular region.
Source: NCBI Gene 112577462 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001395277
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:53904 |
| Approved symbol | OOSP4A |
| Name | oocyte secreted protein family member 4A |
| Location | 11q12.1 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000285010 |
| Ensembl biotype | protein_coding |
| Entrez | 112577462 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000645590
RefSeq mRNA: 1 — MANE Select: NM_001395277
NM_001395277
CCDS: CCDS91479
Canonical transcript exons
ENST00000643613 — 0 exons
Expression profiles
Bgee: expression breadth broad, 57 present calls, max score 42.87.
Top tissues by expression
100 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| blood | UBERON:0000178 | 42.87 | gold quality |
| metanephros cortex | UBERON:0010533 | 42.40 | gold quality |
| cortical plate | UBERON:0005343 | 41.70 | gold quality |
| adult mammalian kidney | UBERON:0000082 | 39.61 | gold quality |
| anterior cingulate cortex | UBERON:0009835 | 38.59 | gold quality |
| cortex of kidney | UBERON:0001225 | 38.38 | gold quality |
| right frontal lobe | UBERON:0002810 | 38.24 | gold quality |
| dorsolateral prefrontal cortex | UBERON:0009834 | 37.68 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| cerebral cortex | UBERON:0000956 | 37.00 | gold quality |
| kidney | UBERON:0002113 | 36.91 | gold quality |
| frontal cortex | UBERON:0001870 | 36.61 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| endometrium | UBERON:0001295 | 36.21 | silver quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| Brodmann (1909) area 9 | UBERON:0013540 | 36.04 | gold quality |
| islet of Langerhans | UBERON:0000006 | 35.98 | gold quality |
| prefrontal cortex | UBERON:0000451 | 35.98 | gold quality |
| Ammon’s horn | UBERON:0001954 | 35.73 | gold quality |
| spleen | UBERON:0002106 | 35.56 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| vermiform appendix | UBERON:0001154 | 35.10 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 35.00 | silver quality |
| cerebellar cortex | UBERON:0002129 | 34.56 | silver quality |
| cerebellar hemisphere | UBERON:0002245 | 34.49 | silver quality |
| cerebellum | UBERON:0002037 | 34.40 | silver quality |
| right uterine tube | UBERON:0001302 | 34.21 | gold quality |
| substantia nigra | UBERON:0002038 | 33.98 | gold quality |
| primary visual cortex | UBERON:0002436 | 33.85 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 33.71 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
Cross-species orthologs
0 orthologs
Protein
Protein identifiers
Oocyte-secreted protein 4A — A0A2R8YFL7 (reviewed: A0A2R8YFL7)
All UniProt accessions (1): A0A2R8YFL7
UniProt curated annotations — full annotation on UniProt →
Subcellular location. Secreted.
Similarity. Belongs to the PLAC1 family.
RefSeq proteins (1): NP_001382206* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR033222 | PLAC1_fam | Family |
UniProt features (3 total): signal peptide 1, chain 1, glycosylation site 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-A0A2R8YFL7-F1 | 70.78 | 0.36 |
Functional residue map
Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.
Glycosylation sites (1): 128
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 1 (showing top):
chr11q12
GO Biological Process (0):
GO Molecular Function (0):
GO Cellular Component (1): extracellular region (GO:0005576)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| cellular anatomical structure | 1 |
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
0 interactions, top by confidence:
ESM2 similar proteins: A0A0A6YXX9, A0A1Z2R986, A0A2R8Y4Y8, A0A2R8YFL7, A0A2R8YFM6, A0A8J1K1A4, A6MFL5, A6MFL6, A6MFL7, A6NHS7, A8MZH6, F8RKW5, G5E8D7, O54767, O77726, O88393, P17219, P20239, P26342, P34128, P35054, P42099, P47983, P47984, P70041, Q03167, Q05996, Q07G34, Q14CH0, Q1W7Q6, Q2Q0J1, Q3HXY1, Q3HXY2, Q3HXY3, Q3HXY4, Q3HXY5, Q3HXY6, Q3HXY8, Q3HXZ1, Q4FZG8
Diamond homologs: A0A2R8YFL7, Q2Q0J1, Q9HBJ0, A0A2R8YFM6, A8MZH6, Q925U0, Q4FZG8, Q4V7E2, Q86WS3, Q9JI83
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1000124571 (11:59968912 T>G), RS1001183350 (11:59963613 T>G), RS1002125771 (11:59968856 G>C), RS1003673282 (11:59965048 T>A), RS1004518469 (11:59964525 A>C,G), RS1004895165 (11:59965129 CG>C,CGGG), RS1005177811 (11:59964125 G>A,T), RS1005509285 (11:59962482 T>A), RS1005931406 (11:59963082 T>C), RS1006147990 (11:59969964 C>T), RS1006191534 (11:59962894 C>A,G), RS1006225309 (11:59968720 A>G), RS1006531018 (11:59970265 A>G), RS1007392409 (11:59968271 C>T), RS1007676199 (11:59962280 A>G)
Disease associations
OMIM: gene `` | disease phenotypes:
GenCC curated gene-disease
Mondo (0):
Orphanet (0):
HPO phenotypes
0 total (0 of 0 shown, HPO-id order):
GWAS associations
0 associations (top):
Drugs & pharmacology
Drug and pharmacology data
Is drug target: no
PharmGKB: 1 entry (VIP=true, CPIC=false)
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.