CXorf58

gene
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Also known as FLJ25444

Summary

CXorf58 (chromosome X open reading frame 58, HGNC:26356) is a protein-coding gene on chromosome Xp22.11, encoding Uncharacterized protein CXorf58 (Q96LI9).

At a glance

  • Clinical variants (ClinVar): 52 total
  • MANE Select transcript: NM_152761

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:26356
Approved symbolCXorf58
Namechromosome X open reading frame 58
LocationXp22.11
Locus typegene with protein product
StatusApproved
AliasesFLJ25444
Ensembl geneENSG00000165182
Ensembl biotypeprotein_coding
Entrez254158

Gene structure

Transcript identifiers

Ensembl transcripts: 4 — 4 protein_coding

ENST00000379211, ENST00000435707, ENST00000648352, ENST00000899642

RefSeq mRNA: 2 — MANE Select: NM_152761 NM_001169574, NM_152761

CCDS: CCDS14209

Canonical transcript exons

ENST00000379211 — 9 exons

ExonStartEnd
ENSE000010910442393854723938700
ENSE000010910452393519623935425
ENSE000010910482392723923927370
ENSE000010910492391175723911856
ENSE000010910512391621723916328
ENSE000010910522391570023915794
ENSE000014801102391028323910418
ENSE000014801112390800623908329
ENSE000038341862393924423939509

Expression profiles

Bgee: expression breadth broad, 90 present calls, max score 85.82.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047385.82gold quality
spermCL:000001977.35gold quality
buccal mucosa cellCL:000233674.49silver quality
testisUBERON:000047361.76gold quality
left testisUBERON:000453361.76gold quality
right testisUBERON:000453461.38gold quality
olfactory segment of nasal mucosaUBERON:000538657.71gold quality
hindlimb stylopod muscleUBERON:000425256.97gold quality
islet of LangerhansUBERON:000000655.98gold quality
bronchial epithelial cellCL:000232855.66silver quality
bronchusUBERON:000218554.95silver quality
right uterine tubeUBERON:000130252.99gold quality
oviduct epitheliumUBERON:000480451.90gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099151.79gold quality
nasal cavity mucosaUBERON:000182648.86gold quality
pancreasUBERON:000126447.04gold quality
fallopian tubeUBERON:000388946.98gold quality
right adrenal gland cortexUBERON:003582746.56gold quality
right adrenal glandUBERON:000123346.46gold quality
left adrenal glandUBERON:000123446.38gold quality
adrenal glandUBERON:000236945.47gold quality
heart left ventricleUBERON:000208445.04gold quality
cardiac ventricleUBERON:000208244.87gold quality
adrenal tissueUBERON:001830344.76silver quality
skeletal muscle tissueUBERON:000113444.67silver quality
lower esophagus mucosaUBERON:003583444.60silver quality
adrenal cortexUBERON:000123544.16gold quality
left adrenal gland cortexUBERON:003582543.93gold quality
skeletal muscle tissue of rectus abdominisUBERON:000451143.37gold quality
muscle tissueUBERON:000238543.34silver quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes3.38

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

16 targeting CXorf58, 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-453499.9966.581907
HSA-MIR-4789-3P99.9970.752484
HSA-MIR-808299.9567.271170
HSA-MIR-46699.6770.852863
HSA-MIR-4743-3P99.6268.122095
HSA-MIR-448099.4266.02735
HSA-MIR-6853-3P99.3670.791558
HSA-MIR-145-3P99.3367.66764
HSA-MIR-6719-3P99.2967.781387
HSA-MIR-1911-3P99.1566.17528
HSA-MIR-1226-3P97.5166.321063
HSA-MIR-4445-5P97.2166.16832
HSA-MIR-6730-3P97.0367.54889
HSA-MIR-301A-5P96.8868.07931
HSA-MIR-301B-5P96.8867.75946
HSA-MIR-6753-5P94.7064.08470

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusFam90a1bENSMUSG00000118554
rattus_norvegicusCxhxorf58ENSRNOG00000051365

Protein

Protein identifiers

Uncharacterized protein CXorf58Q96LI9 (reviewed: Q96LI9)

All UniProt accessions (3): A0A3B3ISQ8, H7C2Q7, Q96LI9

RefSeq proteins (2): NP_001163045, NP_689974* (*=MANE)

Domains & families (InterPro)

UniProt features (4 total): sequence variant 2, chain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q96LI9-F176.340.35

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 40 (showing top): CAGCTG_AP4_Q5, TGIF_01, CYTAGCAAY_UNKNOWN, RFX1_01, DODD_NASOPHARYNGEAL_CARCINOMA_DN, VDR_Q6, chrXp22, PEDRIOLI_MIR31_TARGETS_UP, H1_6_TARGET_GENES, ZBTB12_TARGET_GENES, ZFHX3_TARGET_GENES, ZNF10_TARGET_GENES, ZNF329_TARGET_GENES, ZNF407_TARGET_GENES, ZNF597_TARGET_GENES

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

158 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CXorf58C19orf81C9J6K1771
CXorf58SMLR1H3BR10770
CXorf58AXDND1Q5T1B0694
CXorf58C7orf25Q9BPX7666
CXorf58RSRP1Q9BUV0607
CXorf58CIMIP1Q9H1P6582
CXorf58CFAP46Q8IYW2573
CXorf58ZBTB21Q9ULJ3512
CXorf58SPRP35270473
CXorf58TEX261Q6UWH6445
CXorf58SLC25A52Q3SY17419
CXorf58ATAD3CQ5T2N8355
CXorf58RASGEF1AQ8N9B8311
CXorf58SLC25A51Q9H1U9305
CXorf58RGS1Q08116301

IntAct

5 interactions, top by confidence:

ABTypeScore
CXorf58GDE1psi-mi:“MI:0915”(physical association)0.560
CXorf58H2BC9psi-mi:“MI:0915”(physical association)0.400
CXorf58DCAF5psi-mi:“MI:0915”(physical association)0.400
CXorf58TGFBR2psi-mi:“MI:0914”(association)0.350

BioGRID (8): GDE1 (Affinity Capture-MS), GDE1 (Affinity Capture-MS), CXorf58 (Synthetic Lethality), CXorf58 (Proximity Label-MS), HOXA1 (Affinity Capture-MS), GDE1 (Affinity Capture-MS), TGFBR2 (Affinity Capture-MS), DCAF5 (Affinity Capture-MS)

ESM2 similar proteins: A0A571BF63, A0A5F8MPE6, A1A535, A8QHQ0, B0W730, O23463, O46470, O54829, O64851, O82645, P49758, P49802, P49803, P49809, Q058N0, Q0VA04, Q14D04, Q28IH8, Q4R6I5, Q4R7Z7, Q502W7, Q569B9, Q5PQS3, Q5SPP5, Q5XG48, Q5XIR8, Q641A2, Q6ZQ18, Q7T0S7, Q86VD1, Q8BG67, Q8BMD7, Q8CDN8, Q8H1E8, Q8IGJ0, Q8N957, Q8NCR3, Q8NHS4, Q96L03, Q96LI9

Diamond homologs: A0A5F8MPE6, Q96LI9

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

52 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance3
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

1537 predictions. Top by Δscore:

VariantEffectΔscore
X:23910277:TTTCA:Tacceptor_loss1.0000
X:23910278:TTCA:Tacceptor_loss1.0000
X:23910281:A:Tacceptor_loss1.0000
X:23910414:CTATC:Cdonor_gain1.0000
X:23910419:G:GGdonor_gain1.0000
X:23916283:TTAC:Tdonor_gain1.0000
X:23916324:G:GGdonor_gain1.0000
X:23927235:A:AGacceptor_gain1.0000
X:23927237:A:AGacceptor_gain1.0000
X:23927237:A:Gacceptor_loss1.0000
X:23927237:AG:Aacceptor_gain1.0000
X:23927238:G:GAacceptor_gain1.0000
X:23927238:GG:Gacceptor_gain1.0000
X:23927238:GGC:Gacceptor_gain1.0000
X:23927238:GGCA:Gacceptor_gain1.0000
X:23927320:TCCA:Tdonor_gain1.0000
X:23927326:G:GGdonor_gain1.0000
X:23927371:G:GGdonor_gain1.0000
X:23935403:C:Gdonor_gain1.0000
X:23907951:G:GTdonor_gain0.9900
X:23908182:G:GTdonor_gain0.9900
X:23908233:G:GTdonor_gain0.9900
X:23910281:A:AGacceptor_gain0.9900
X:23910282:G:GGacceptor_gain0.9900
X:23910282:GATT:Gacceptor_gain0.9900
X:23910415:TATCG:Tdonor_loss0.9900
X:23910416:ATC:Adonor_gain0.9900
X:23910416:ATCGT:Adonor_loss0.9900
X:23910417:TC:Tdonor_gain0.9900
X:23910417:TCG:Tdonor_loss0.9900

AlphaMissense

2193 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
X:23935250:T:AW204R0.994
X:23935250:T:CW204R0.994
X:23916233:T:CF110L0.992
X:23916235:T:AF110L0.992
X:23916235:T:GF110L0.992
X:23935254:G:CR205P0.991
X:23915791:T:CF103S0.990
X:23916251:T:CF116L0.989
X:23916253:T:AF116L0.989
X:23916253:T:GF116L0.989
X:23916255:A:TK117I0.988
X:23911824:T:CF62L0.987
X:23911826:T:AF62L0.987
X:23911826:T:GF62L0.987
X:23935253:C:AR205S0.987
X:23916219:T:CF105S0.986
X:23935252:G:CW204C0.986
X:23935252:G:TW204C0.986
X:23916256:A:CK117N0.982
X:23916256:A:TK117N0.982
X:23911831:T:CL64P0.980
X:23935260:T:CL207S0.979
X:23911834:T:CL65P0.978
X:23935299:A:TD220V0.977
X:23915748:G:CA89P0.976
X:23935246:C:AN202K0.974
X:23935246:C:GN202K0.974
X:23935299:A:CD220A0.974
X:23916240:C:AP112H0.973
X:23916254:A:GK117E0.972

dbSNP variants (sampled 300 via entrez): RS1000277974 (X:23911588 AT>A), RS1000394046 (X:23929924 G>A), RS1000451000 (X:23912465 C>T), RS1000880066 (X:23908802 A>G), RS1000929118 (X:23912125 G>A), RS1000985429 (X:23921440 T>C), RS1001039253 (X:23921038 A>T), RS1001128296 (X:23937376 T>C), RS1001463195 (X:23911465 A>G), RS1001904584 (X:23920385 A>G), RS1002090229 (X:23911222 T>A,C), RS1002240171 (X:23920781 C>T), RS1002252459 (X:23920319 G>A), RS1002308636 (X:23929837 A>G), RS1002455439 (X:23907402 G>A)

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)

CTD chemical–gene interactions

6 total (human), top 6 by PubMed support.

ChemicalActions (top 5)PubMed papers
S-(1,2-dichlorovinyl)cysteineincreases expression, affects cotreatment, affects response to substance1
abrineincreases expression1
Benzo(a)pyreneincreases methylation, affects methylation1
Carbamazepineaffects expression1
Lipopolysaccharidesaffects cotreatment, affects response to substance, increases expression1
Valproic Acidincreases methylation1

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.