CXorf51B
gene geneOn this page
Summary
CXorf51B (chromosome X open reading frame 51B, HGNC:42787) is a protein-coding gene on chromosome Xq27.3, encoding Uncharacterized protein CXorf51B (P0DPH9).
At a glance
- MANE Select transcript:
NM_001244892
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:42787 |
| Approved symbol | CXorf51B |
| Name | chromosome X open reading frame 51B |
| Location | Xq27.3 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000235699 |
| Ensembl biotype | protein_coding |
| Entrez | 100133053 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000438525
RefSeq mRNA: 1 — MANE Select: NM_001244892
NM_001244892
CCDS: CCDS83497
Canonical transcript exons
ENST00000438525 — 2 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001599806 | 146809771 | 146809923 |
| ENSE00001729559 | 146810114 | 146810411 |
Expression profiles
Bgee: expression breadth broad, 31 present calls, max score 96.19.
FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0113 / max 9.9239, expressed in 3 samples.
FANTOM5 promoters (1 alternative TSS)
| Promoter ID | TPM avg | Samples expressed |
|---|---|---|
| 209852 | 0.0113 | 3 |
Top tissues by expression
121 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| left testis | UBERON:0004533 | 96.19 | gold quality |
| testis | UBERON:0000473 | 95.85 | gold quality |
| right testis | UBERON:0004534 | 95.73 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 95.38 | gold quality |
| sural nerve | UBERON:0015488 | 37.71 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 33.38 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| muscle tissue | UBERON:0002385 | 31.06 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| monocyte | CL:0000576 | 29.18 | silver quality |
| tonsil | UBERON:0002372 | 29.13 | gold quality |
| leukocyte | CL:0000738 | 29.04 | silver quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| liver | UBERON:0002107 | 28.04 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| blood | UBERON:0000178 | 26.96 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.55 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| gall bladder | UBERON:0002110 | 25.98 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 25.89 | gold quality |
| placenta | UBERON:0001987 | 25.81 | gold quality |
| urinary bladder | UBERON:0001255 | 25.72 | gold quality |
| muscle of leg | UBERON:0001383 | 25.23 | gold quality |
| primary visual cortex | UBERON:0002436 | 24.61 | gold 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
miRNA regulators (miRDB)
8 targeting CXorf51B, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-552-5P | 99.93 | 68.56 | 1583 |
| HSA-MIR-4420 | 99.82 | 70.08 | 1624 |
| HSA-MIR-181B-2-3P | 99.81 | 70.06 | 1646 |
| HSA-MIR-181B-3P | 99.81 | 70.06 | 1646 |
| HSA-MIR-11399 | 98.71 | 65.69 | 869 |
| HSA-MIR-653-3P | 98.31 | 67.71 | 1542 |
| HSA-MIR-649 | 97.96 | 67.21 | 704 |
| HSA-MIR-490-3P | 97.79 | 65.54 | 606 |
Cross-species orthologs
0 orthologs
Paralogs (1): CXorf51A (ENSG00000224440)
Protein
Protein identifiers
Uncharacterized protein CXorf51B — P0DPH9 (reviewed: P0DPH9)
All UniProt accessions (1): P0DPH9
RefSeq proteins (1): NP_001231821* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR040433 | Spermatid_TP | Family |
UniProt features (6 total): compositionally biased region 4, chain 1, region of interest 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0DPH9-F1 | 68.70 | 0.00 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 1 (showing top):
chrXq27
GO Biological Process (0):
GO Molecular Function (1): protein binding (GO:0005515)
GO Cellular Component (0):
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| binding | 1 |
Protein interactions and networks
STRING
0 interactions, top by confidence (×1000):
IntAct
4 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| CXorf51B | AP2M1 | psi-mi:“MI:0915”(physical association) | 0.560 |
| CXorf51B | AP2M1 | psi-mi:“MI:0915”(physical association) | 0.000 |
ESM2 similar proteins: A0A1B0GTR3, A0A7H0DN82, A7RR34, E9PVX6, O14598, O60356, O60829, O94243, P04605, P04614, P05909, P0C1K0, P0C765, P0C766, P0DPH9, P17285, P17759, P18098, P19416, P20290, P24109, P46012, P46583, Q06428, Q07555, Q08561, Q09821, Q1L9C7, Q32PF3, Q3KP22, Q5M948, Q5M951, Q5MJ08, Q5RCI9, Q6P8I4, Q758T8, Q76632, Q7M2N1, Q7TP40, Q80WR5
Diamond homologs: A0A1B0GTR3, P0DPH9
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
688 scored. Top likely-pathogenic:
dbSNP variants (sampled 6 via entrez): RS1557052030 (X:146809744 T>C), RS1557052032 (X:146809918 G>A), RS1557052034 (X:146810110 G>A), RS879333579 (X:146808773 T>C), RS879685486 (X:146808500 C>T), RS879953135 (X:146809765 G>C)
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.