CXorf51B

gene
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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

FieldValue
HGNC IDHGNC:42787
Approved symbolCXorf51B
Namechromosome X open reading frame 51B
LocationXq27.3
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000235699
Ensembl biotypeprotein_coding
Entrez100133053

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

ExonStartEnd
ENSE00001599806146809771146809923
ENSE00001729559146810114146810411

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 IDTPM avgSamples expressed
2098520.01133

Top tissues by expression

121 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
left testisUBERON:000453396.19gold quality
testisUBERON:000047395.85gold quality
right testisUBERON:000453495.73gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047395.38gold quality
sural nerveUBERON:001548837.71gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
muscle tissueUBERON:000238531.06gold quality
stromal cell of endometriumCL:000225529.87gold quality
monocyteCL:000057629.18silver quality
tonsilUBERON:000237229.13gold quality
leukocyteCL:000073829.04silver quality
duodenumUBERON:000211428.14gold quality
liverUBERON:000210728.04gold quality
lymph nodeUBERON:000002927.57gold quality
bloodUBERON:000017826.96gold quality
islet of LangerhansUBERON:000000626.55gold quality
vermiform appendixUBERON:000115426.42gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
urinary bladderUBERON:000125525.72gold quality
muscle of legUBERON:000138325.23gold quality
primary visual cortexUBERON:000243624.61gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.00

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):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-552-5P99.9368.561583
HSA-MIR-442099.8270.081624
HSA-MIR-181B-2-3P99.8170.061646
HSA-MIR-181B-3P99.8170.061646
HSA-MIR-1139998.7165.69869
HSA-MIR-653-3P98.3167.711542
HSA-MIR-64997.9667.21704
HSA-MIR-490-3P97.7965.54606

Cross-species orthologs

0 orthologs

Paralogs (1): CXorf51A (ENSG00000224440)

Protein

Protein identifiers

Uncharacterized protein CXorf51BP0DPH9 (reviewed: P0DPH9)

All UniProt accessions (1): P0DPH9

RefSeq proteins (1): NP_001231821* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR040433Spermatid_TPFamily

UniProt features (6 total): compositionally biased region 4, chain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-P0DPH9-F168.700.00

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:

CategoryTerms
binding1

Protein interactions and networks

STRING

0 interactions, top by confidence (×1000):

IntAct

4 interactions, top by confidence:

ABTypeScore
CXorf51BAP2M1psi-mi:“MI:0915”(physical association)0.560
CXorf51BAP2M1psi-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):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

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.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.