TEX30

gene
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Summary

TEX30 (testis expressed 30, HGNC:25188) is a protein-coding gene on chromosome 13q33.1, encoding Testis-expressed protein 30 (Q5JUR7).

At a glance

  • Clinical variants (ClinVar): 28 total
  • Druggable target: yes
  • MANE Select transcript: NM_138779

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25188
Approved symbolTEX30
Nametestis expressed 30
Location13q33.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000151287
Ensembl biotypeprotein_coding
Entrez93081

Gene structure

Transcript identifiers

Ensembl transcripts: 19 — 18 protein_coding, 1 protein_coding_CDS_not_defined

ENST00000376019, ENST00000376021, ENST00000376022, ENST00000376027, ENST00000376029, ENST00000376032, ENST00000487260, ENST00000851861, ENST00000851862, ENST00000851863, ENST00000851864, ENST00000851865, ENST00000851866, ENST00000851867, ENST00000851868, ENST00000851869, ENST00000913262, ENST00000913263, ENST00000913264

RefSeq mRNA: 3 — MANE Select: NM_138779 NM_001286775, NM_001286776, NM_138779

CCDS: CCDS66577, CCDS66578, CCDS9503

Canonical transcript exons

ENST00000376032 — 6 exons

ExonStartEnd
ENSE00000998722102767273102767478
ENSE00001092522102768260102768311
ENSE00003598813102769311102769541
ENSE00003667690102770012102770086
ENSE00003841566102765888102766580
ENSE00003846141102773682102773786

Expression profiles

Bgee: expression breadth ubiquitous, 243 present calls, max score 98.30.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 13.6604 / max 238.1729, expressed in 1774 samples.

FANTOM5 promoters (2 alternative TSS)

Promoter IDTPM avgSamples expressed
13810910.54271765
1381083.11771211

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
right testisUBERON:000453498.30gold quality
left testisUBERON:000453398.25gold quality
testisUBERON:000047397.04gold quality
adult organismUBERON:000702395.90gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047395.50gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099195.38gold quality
spermCL:000001994.45gold quality
male germ cellCL:000001594.12gold quality
corpus epididymisUBERON:000435990.83gold quality
right lobe of liverUBERON:000111490.13gold quality
ventricular zoneUBERON:000305389.77gold quality
endometrium epitheliumUBERON:000481187.82silver quality
ganglionic eminenceUBERON:000402387.70gold quality
islet of LangerhansUBERON:000000686.59gold quality
liverUBERON:000210786.59gold quality
metanephros cortexUBERON:001053385.50gold quality
cauda epididymisUBERON:000436083.78gold quality
oocyteCL:000002383.71gold quality
embryoUBERON:000092283.58gold quality
adult mammalian kidneyUBERON:000008283.39gold quality
hindlimb stylopod muscleUBERON:000425283.32gold quality
cingulate cortexUBERON:000302782.52gold quality
anterior cingulate cortexUBERON:000983582.39gold quality
gastrocnemiusUBERON:000138882.29gold quality
placentaUBERON:000198782.16gold quality
stromal cell of endometriumCL:000225582.00gold quality
Brodmann (1909) area 9UBERON:001354081.93gold quality
muscle of legUBERON:000138381.89gold quality
body of uterusUBERON:000985381.76gold quality
cerebellar hemisphereUBERON:000224581.64gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 2.

ExperimentMarker?Max mean expression
E-GEOD-134144yes1291.47
E-ANND-3yes6.79

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

47 targeting TEX30, 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-LET-7A-3P100.0074.033932
HSA-LET-7B-3P100.0074.083913
HSA-LET-7F-1-3P100.0074.023928
HSA-MIR-98-3P100.0074.083907
HSA-MIR-186-5P99.9970.833707
HSA-MIR-477599.9875.006394
HSA-MIR-60799.9773.625593
HSA-MIR-23A-3P99.9574.243163
HSA-MIR-23B-3P99.9574.243163
HSA-MIR-23C99.9573.923192
HSA-MIR-130599.9171.433443
HSA-MIR-132399.8369.892471
HSA-MIR-520F-3P99.8271.321216
HSA-MIR-313399.8170.923506
HSA-MIR-3617-5P99.7569.411968
HSA-MIR-64199.7569.351975
HSA-MIR-548O-3P99.7469.302228
HSA-MIR-494-3P99.7071.452795
HSA-MIR-510-3P99.5470.062965
HSA-MIR-16-2-3P99.2970.601954
HSA-MIR-195-3P99.2970.611954
HSA-MIR-18A-5P99.2971.05806
HSA-MIR-18B-5P99.2971.05806
HSA-MIR-3160-5P99.2869.071938
HSA-MIR-4735-3P99.1469.85777
HSA-MIR-807099.0769.301303
HSA-MIR-194-5P99.0169.651465
HSA-MIR-4709-3P98.8868.041594
HSA-MIR-374A-3P98.8767.821531
HSA-MIR-3194-3P98.8366.221167

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusTex30ENSMUSG00000026049
rattus_norvegicusTex30ENSRNOG00000011658

Paralogs (1): KANSL3 (ENSG00000114982)

Protein

Protein identifiers

Testis-expressed protein 30Q5JUR7 (reviewed: Q5JUR7)

All UniProt accessions (3): Q5JUR7, A0A0C4DFW4, Q5JUS0

UniProt curated annotations — full annotation on UniProt →

Isoforms (2)

UniProt IDNamesCanonical?
Q5JUR7-11yes
Q5JUR7-22

RefSeq proteins (3): NP_001273704, NP_001273705, NP_620134* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR026555NSL3/Tex30Family
IPR029058AB_hydrolase_foldHomologous_superfamily
IPR046879KANL3/Tex30_AbhydrolaseDomain

Pfam: PF20408

UniProt features (3 total): splice variant 2, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q5JUR7-F194.240.89

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 152 (showing top): DACOSTA_UV_RESPONSE_VIA_ERCC3_UP, BROWNE_HCMV_INFECTION_16HR_UP, GROSS_HYPOXIA_VIA_ELK3_AND_HIF1A_DN, SCHAEFFER_PROSTATE_DEVELOPMENT_6HR_UP, FISCHER_DREAM_TARGETS, KOBAYASHI_EGFR_SIGNALING_24HR_DN, NUYTTEN_EZH2_TARGETS_DN, YAGI_AML_WITH_11Q23_REARRANGED, LINDGREN_BLADDER_CANCER_CLUSTER_1_DN, GEORGES_TARGETS_OF_MIR192_AND_MIR215, PUIFFE_INVASION_INHIBITED_BY_ASCITES_DN, MARTENS_TRETINOIN_RESPONSE_DN, CHICAS_RB1_TARGETS_SENESCENT, WANG_RESPONSE_TO_GSK3_INHIBITOR_SB216763_DN, BRUINS_UVC_RESPONSE_LATE

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

512 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TEX30TEX29Q8N6K0605
TEX30FAM9CQ8IZT9533
TEX30TEX13CA0A0J9YWL9472
TEX30TEX12Q9BXU0465
TEX30ABHD16BQ9H3Z7430
TEX30TEKT5Q96M29427
TEX30C14orf39Q8N1H7406
TEX30CCT6BQ92526402
TEX30PSMA8Q8TAA3392
TEX30CENPNQ96H22392
TEX30ABHD13Q7L211390
TEX30TEX13AQ9BXU3387
TEX30TEX36Q5VZQ5386
TEX30MEIOBQ8N635385
TEX30TEX13DA0A0J9YY54382
TEX30TEX22C9J3V5382

IntAct

2 interactions, top by confidence:

ABTypeScore
TEX30SHTN1psi-mi:“MI:0914”(association)0.350

BioGRID (7): PREPL (Affinity Capture-MS), KIAA1598 (Affinity Capture-MS), TEX30 (Protein-peptide), TEX30 (Cross-Linking-MS (XL-MS)), TEX30 (Two-hybrid), TEX30 (Affinity Capture-RNA), TEX30 (Affinity Capture-RNA)

ESM2 similar proteins: A0A7H0DN16, A5PJJ7, B5BLW5, D5H0J3, G5EDL5, O16925, O17795, O22898, O57245, O60095, O74427, O74628, O74878, P28321, P32604, P42840, P54069, P78898, P93711, P96084, Q17704, Q1ZXQ4, Q3TUU5, Q3ZC52, Q4JK73, Q54DM9, Q54K57, Q54NU9, Q556J2, Q5JUR7, Q5M875, Q5UQ83, Q5ZJL8, Q6AYS8, Q6IRP4, Q6QA32, Q7L211, Q7Z5P4, Q80UX8, Q8NBQ5

Diamond homologs: Q3TUU5, Q3ZC52, Q5JUR7

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance19
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

764 predictions. Top by Δscore:

VariantEffectΔscore
13:102766581:C:CCacceptor_gain1.0000
13:102768255:CTTA:Cdonor_loss1.0000
13:102768256:TTA:Tdonor_loss1.0000
13:102768257:TACCT:Tdonor_loss1.0000
13:102768258:A:ACdonor_gain1.0000
13:102768258:ACCT:Adonor_gain1.0000
13:102768259:C:CCdonor_gain1.0000
13:102768259:CCT:Cdonor_gain1.0000
13:102768259:CCTC:Cdonor_gain1.0000
13:102768307:TAATT:Tacceptor_gain1.0000
13:102768308:AATT:Aacceptor_gain1.0000
13:102768309:ATT:Aacceptor_gain1.0000
13:102768310:TT:Tacceptor_gain1.0000
13:102768311:TCT:Tacceptor_loss1.0000
13:102768312:C:CCacceptor_gain1.0000
13:102768312:CTAGA:Cacceptor_loss1.0000
13:102768313:T:Gacceptor_loss1.0000
13:102773677:CTTA:Cdonor_loss1.0000
13:102773678:TTAC:Tdonor_loss1.0000
13:102773679:TA:Tdonor_loss1.0000
13:102773680:AC:Adonor_gain1.0000
13:102773681:C:CTdonor_loss1.0000
13:102773681:CC:Cdonor_gain1.0000
13:102766579:TT:Tacceptor_gain0.9900
13:102767272:CCTTT:Cdonor_gain0.9900
13:102768258:AC:Adonor_gain0.9900
13:102768258:ACCTC:Adonor_gain0.9900
13:102768259:CC:Cdonor_gain0.9900
13:102768259:CCTCC:Cdonor_gain0.9900
13:102768312:CTA:Cacceptor_gain0.9900

AlphaMissense

1498 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
13:102769365:A:CF64L0.997
13:102769365:A:TF64L0.997
13:102769367:A:GF64L0.997
13:102767473:A:GS102P0.996
13:102769335:T:AR74S0.996
13:102769335:T:GR74S0.996
13:102767290:C:GD163H0.995
13:102769366:A:GF64S0.994
13:102766509:A:CH192Q0.993
13:102766509:A:TH192Q0.993
13:102767289:T:AD163V0.992
13:102769336:C:GR74T0.992
13:102767454:G:TA108D0.991
13:102767459:T:AR106S0.991
13:102767459:T:GR106S0.991
13:102766511:G:CH192D0.990
13:102767472:G:AS102L0.990
13:102767289:T:GD163A0.989
13:102767345:T:AR144S0.989
13:102767345:T:GR144S0.989
13:102767392:A:GC129R0.989
13:102767467:C:GG104R0.989
13:102767279:A:CC166W0.988
13:102767298:C:TG160D0.988
13:102767310:A:GL156P0.988
13:102769315:A:TV81D0.988
13:102767397:A:GL127P0.987
13:102767467:C:AG104C0.987
13:102769325:A:CY78D0.987
13:102769372:A:GL62P0.987

dbSNP variants (sampled 300 via entrez): RS1000266447 (13:102770253 G>A), RS1000355133 (13:102766906 T>C), RS1000379584 (13:102766647 C>A,T), RS1000576046 (13:102773873 C>A,G,T), RS1000871524 (13:102768746 T>C), RS1001824745 (13:102769030 T>A), RS1001909083 (13:102767413 C>T), RS1001970553 (13:102774372 C>T), RS1002029455 (13:102773567 T>C), RS1002323712 (13:102767165 G>A,T), RS1002856685 (13:102765405 AATT>A), RS1002920396 (13:102769094 G>A), RS1003067172 (13:102775543 C>G), RS1004370142 (13:102770342 G>A), RS1004560274 (13:102773773 C>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: yes

ChEMBL targets (1): CHEMBL2189125 (SINGLE PROTEIN)

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

39 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, increases expression2
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxidedecreases expression, increases expression2
afuresertibdecreases expression1
triphenyl phosphateaffects expression1
bisphenol Adecreases expression1
sodium arseniteincreases expression1
potassium chromate(VI)affects cotreatment, decreases expression1
2,3-bis(3’-hydroxybenzyl)butyrolactoneaffects cotreatment, increases expression1
cupric chlorideincreases expression1
epigallocatechin gallatedecreases expression, affects cotreatment1
perfluorooctane sulfonic aciddecreases expression1
monomethylarsonous aciddecreases expression1
jinfukangdecreases expression1
4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic aciddecreases expression1
Dasatinibdecreases expression1
Resveratrolaffects cotreatment, increases expression1
Sunitinibincreases expression1
Vorinostatincreases expression1
Acetaminophenincreases expression1
Benzeneincreases expression1
Benzo(a)pyreneincreases expression1
Calcitrioldecreases expression, affects cotreatment1
Cisplatinincreases expression1
Coumestrolaffects cotreatment, increases expression1
Cyclophosphamidedecreases expression1
Golddecreases expression1
Ivermectindecreases expression1
Melphalanincreases expression1
Methyl Methanesulfonateincreases expression1
Silicon Dioxideincreases expression1

ChEMBL screening assays

1 unique, capped per target: 1 binding

Representative assays (with source publication via chembl_document):

Assay IDTypeDescriptionSource paper
CHEMBL2209079BindingInhibition of C13orf27 binding to FP-biotin in [12C][14N]-lysine, arginine and [13C6][15N2]-lysine, arginine labeled HEK293T cells at 20 uM after 1 hr by isotopic activity-based protein profiling-MudPIT assayDiscovery and optimization of sulfonyl acrylonitriles as selective, covalent inhibitors of protein phosphatase methylesterase-1. — J Med Chem

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.