TDRD15

gene
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Summary

TDRD15 (tudor domain containing 15, HGNC:45037) is a protein-coding gene on chromosome 2p24.1, encoding Tudor domain-containing protein 15 (B5MCY1).

At a glance

  • GWAS associations: 31
  • Clinical variants (ClinVar): 1 total
  • MANE Select transcript: NM_001306137

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:45037
Approved symbolTDRD15
Nametudor domain containing 15
Location2p24.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000218819
Ensembl biotypeprotein_coding
Entrez100129278

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000405799, ENST00000622654

RefSeq mRNA: 1 — MANE Select: NM_001306137 NM_001306137

CCDS: CCDS77385

Canonical transcript exons

ENST00000405799 — 4 exons

ExonStartEnd
ENSE000015498352113476221134847
ENSE000015528202112760121127711
ENSE000015573232113746521144368
ENSE000015629542112396821124046

Expression profiles

Bgee: expression breadth broad, 13 present calls, max score 83.19.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047383.19gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099162.27gold quality
testisUBERON:000047359.31gold quality
right testisUBERON:000453458.54gold quality
left testisUBERON:000453356.57gold quality
liverUBERON:000210755.16gold quality
right lobe of liverUBERON:000111454.50gold quality
colonic epitheliumUBERON:000039745.17gold quality
bone marrow cellCL:000209244.64gold quality
sural nerveUBERON:001548839.60gold quality
lymph nodeUBERON:000002939.50gold quality
vermiform appendixUBERON:000115437.64gold quality
monocyteCL:000057637.54gold quality
leukocyteCL:000073837.13gold quality
ventricular zoneUBERON:000305336.48gold quality
hindlimb stylopod muscleUBERON:000425236.47silver quality
cortical plateUBERON:000534336.47gold quality
calcaneal tendonUBERON:000370136.14gold quality
endometriumUBERON:000129536.13gold quality
bone marrowUBERON:000237136.07gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113434.76gold quality
granulocyteCL:000009434.45gold quality
muscle tissueUBERON:000238534.22gold quality
gall bladderUBERON:000211033.24gold quality
rectumUBERON:000105232.79gold quality
placentaUBERON:000198732.24gold quality
urinary bladderUBERON:000125531.22gold quality
bloodUBERON:000017831.08gold quality
uterine cervixUBERON:000000230.39gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes4.06

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

59 targeting TDRD15, 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-5011-5P100.0083.465820
HSA-MIR-340-5P100.0072.504437
HSA-MIR-3613-3P100.0076.367965
HSA-MIR-428299.9975.366408
HSA-MIR-186-5P99.9970.833707
HSA-MIR-366299.9973.825684
HSA-MIR-493-5P99.9672.472382
HSA-MIR-335-3P99.9373.364958
HSA-MIR-338-5P99.9272.342951
HSA-MIR-806399.9169.763146
HSA-MIR-367199.9073.043897
HSA-MIR-808799.9069.551351
HSA-MIR-380-3P99.8970.181978
HSA-MIR-5582-3P99.8672.484221
HSA-MIR-469899.8471.414303
HSA-MIR-6715A-3P99.8368.051473
HSA-MIR-449599.8272.083080
HSA-MIR-4668-5P99.7970.583782
HSA-MIR-120899.7068.281533
HSA-MIR-3059-5P99.7069.932491
HSA-MIR-7161-5P99.6868.921592
HSA-MIR-548U99.6567.781463
HSA-MIR-7152-5P99.6069.332094
HSA-MIR-451B99.5568.281380
HSA-MIR-5007-3P99.5168.141242
HSA-MIR-513C-5P99.5068.421730
HSA-MIR-514B-5P99.5068.191766
HSA-MIR-142-5P99.4870.922416
HSA-MIR-5590-3P99.4870.912429
HSA-MIR-29799.4069.581418

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriotdrd15ENSDARG00000014039
rattus_norvegicusTdrd15ENSRNOG00000060052
drosophila_melanogastertudFBGN0003891

Paralogs (6): TDRD1 (ENSG00000095627), TDRD5 (ENSG00000162782), TDRD10 (ENSG00000163239), TDRD6 (ENSG00000180113), TDRKH (ENSG00000182134), TDRD7 (ENSG00000196116)

Protein

Protein identifiers

Tudor domain-containing protein 15B5MCY1 (reviewed: B5MCY1)

All UniProt accessions (1): B5MCY1

RefSeq proteins (1): NP_001293066* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR002999TudorDomain
IPR035437SNase_OB-fold_sfHomologous_superfamily
IPR047450Tudor_TDRD15_rpt1Domain
IPR047452Tudor_TDRD15_rpt2Domain
IPR047454Tudor_TDRD15_rpt3Domain
IPR047455Tudor_TDRD15_rpt4Domain
IPR047457Tudor_TDRD15_rpt7Domain
IPR047459Tudor_TDRD15_rpt6Domain
IPR047460Tudor_TDRD15_rpt5Domain
IPR050621Tudor_domain_containingFamily

Pfam: PF00567

UniProt features (11 total): domain 8, chain 1, compositionally biased region 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-B5MCY1-F172.130.17

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 20 (showing top): SRSF9_TARGET_GENES, MIR3671, MIR186_5P, MIR513A_3P_MIR513C_3P, MIR4495, MIR410_3P, MIR3124_3P, MIR676_5P, MIR451B, MIR3674, MIR5007_3P, MIR1304_3P, MIR4752, MIR514A_5P, MIR3146

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

722 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TDRD15TDRD12Q587J7560
TDRD15PIWIL3Q7Z3Z3504
TDRD15PIWIL1Q96J94497
TDRD15TDRD5Q8NAT2496
TDRD15TDRD9Q8NDG6494
TDRD15RIMBP3BA6NNM3481
TDRD15CFAP73A6NFT4463
TDRD15TDRKHQ9Y2W6450
TDRD15EXD1Q8NHP7447
TDRD15TDRD7Q8NHU6444
TDRD15FAM24BQ8N5W8439
TDRD15STK31Q9BXU1432
TDRD15PRSS37A4D1T9430
TDRD15RIMBP3CA6NJZ7419
TDRD15PIWIL2Q8TC59417

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0JM98, A1L1H3, A6NAF9, A6QLE1, A9CPT4, B5MCY1, D2H0H6, D2H3M0, D4A7V9, E1BPH3, E1C3S7, E2QTD3, E2RDV1, E7FDW8, F1R237, O60522, P57075, P61407, P97874, Q14B46, Q1L981, Q4R3G4, Q58EK5, Q5DTW2, Q5JTW2, Q5M7P8, Q5RAH6, Q5VCS6, Q5VZ19, Q5XGX5, Q61846, Q68DX3, Q6NU04, Q80VK6, Q8K1H1, Q8NAT2, Q8NHU6, Q90WE3, Q99KY4, Q99MV1

Diamond homologs: A0JM98, A1L1H3, A6NAF9, A9CPT4, B4F7C4, B5MCY1, D2H3M0, E1BPH3, E2QTD3, Q1L981, Q5VCS6, Q8NAT2, Q4R3G4, Q9BXT4, Q99MV7

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

689 predictions. Top by Δscore:

VariantEffectΔscore
2:21130789:T:TAdonor_gain0.9900
2:21130790:A:AAdonor_gain0.9900
2:21130791:G:GGdonor_gain0.9600
2:21134846:GT:Gdonor_gain0.9500
2:21137829:T:TAdonor_gain0.9500
2:21137830:A:AAdonor_gain0.9500
2:21124345:GTGT:Gdonor_gain0.9400
2:21124075:T:Adonor_gain0.9300
2:21124043:CTTGG:Cdonor_loss0.9200
2:21124044:TTGG:Tdonor_loss0.9200
2:21124045:TGG:Tdonor_loss0.9200
2:21124046:GG:Gdonor_loss0.9200
2:21124048:TAAAC:Tdonor_loss0.9200
2:21124049:A:Cdonor_loss0.9200
2:21124296:G:GTdonor_gain0.9200
2:21130769:C:Tdonor_gain0.9200
2:21124349:G:GGdonor_gain0.9100
2:21133623:T:Gdonor_gain0.9100
2:21137463:A:AGacceptor_gain0.9100
2:21137464:G:GGacceptor_gain0.9100
2:21124058:C:Gdonor_gain0.9000
2:21124347:GT:Gdonor_gain0.9000
2:21137464:GAAA:Gacceptor_gain0.8800
2:21124047:G:GGdonor_gain0.8700
2:21137831:G:GGdonor_gain0.8700
2:21134848:G:GGdonor_gain0.8600
2:21124014:G:Tdonor_gain0.8500
2:21124067:T:Gdonor_gain0.8400
2:21124284:T:Gdonor_gain0.8400
2:21124341:GGCT:Gdonor_gain0.8300

AlphaMissense

12807 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
2:21138380:T:AW305R0.993
2:21138380:T:CW305R0.993
2:21137873:T:AW136R0.992
2:21137873:T:CW136R0.992
2:21139117:A:CR550S0.992
2:21139117:A:TR550S0.992
2:21139118:G:CA551P0.992
2:21140557:A:CR1030S0.992
2:21140557:A:TR1030S0.992
2:21138388:A:CR307S0.991
2:21138388:A:TR307S0.991
2:21137701:A:CR78S0.988
2:21137701:A:TR78S0.988
2:21139086:C:AA540D0.988
2:21139119:C:AA551D0.988
2:21137693:T:AW76R0.987
2:21137693:T:CW76R0.987
2:21139116:G:CR550T0.984
2:21141818:T:AW1451R0.984
2:21141818:T:CW1451R0.984
2:21139918:A:CR817S0.983
2:21139918:A:TR817S0.983
2:21142864:A:CR1799S0.983
2:21142864:A:TR1799S0.983
2:21139079:T:CC538R0.981
2:21139289:T:AW608R0.981
2:21139289:T:CW608R0.981
2:21141551:G:CA1362P0.981
2:21138387:G:CR307T0.980
2:21138486:T:AL340H0.980

dbSNP variants (sampled 300 via entrez): RS1000178960 (2:21127435 T>G), RS1000509049 (2:21130373 A>G), RS1000600682 (2:21135385 A>G), RS1000871815 (2:21145653 AT>A), RS1001034727 (2:21135571 A>G), RS1001064053 (2:21129180 A>C), RS1001070753 (2:21122906 A>C), RS1001126590 (2:21131876 A>T), RS1001379385 (2:21125383 C>G,T), RS1001410342 (2:21125014 G>A,T), RS1001428787 (2:21138368 C>T), RS1001440173 (2:21123143 G>A), RS1001584806 (2:21141669 T>G), RS1001863532 (2:21128748 T>C), RS1001970214 (2:21143839 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

31 associations (top):

StudyTraitp-value
GCST008074_88Triglyceride levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df)6.000000e-06
GCST008077_3LDL cholesterol levels9.000000e-57
GCST008077_33LDL cholesterol levels1.000000e-06
GCST008077_39LDL cholesterol levels7.000000e-10
GCST008077_43LDL cholesterol levels5.000000e-14
GCST008077_49LDL cholesterol levels1.000000e-78
GCST008078_135LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df)2.000000e-193
GCST008078_50LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df)2.000000e-11
GCST008078_79LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df)4.000000e-13
GCST008078_87LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df)2.000000e-22
GCST008078_98LDL cholesterol levels x alcohol consumption (regular vs non-regular drinkers) interaction (2df)5.000000e-226
GCST008079_105LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df)5.000000e-213
GCST008079_32LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df)2.000000e-249
GCST008079_78LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df)6.000000e-11
GCST008079_86LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df)1.000000e-14
GCST008079_97LDL cholesterol levels x alcohol consumption (drinkers vs non-drinkers) interaction (2df)3.000000e-23
GCST008086_105LDL cholesterol levels in current drinkers2.000000e-127
GCST008086_109LDL cholesterol levels in current drinkers2.000000e-18
GCST008086_113LDL cholesterol levels in current drinkers2.000000e-101
GCST008086_89LDL cholesterol levels in current drinkers1.000000e-10
GCST008086_96LDL cholesterol levels in current drinkers9.000000e-10
GCST008087_1Triglyceride levels in current drinkers2.000000e-06
GCST010243_118Apolipoprotein B levels9.000000e-12
GCST010244_146Triglyceride levels2.000000e-12
GCST010245_216LDL cholesterol levels2.000000e-103
GCST010480_2Coronary artery disease1.000000e-10
GCST010866_31Coronary artery disease2.000000e-13
GCST011365_84Myocardial infarction4.000000e-07
GCST011679_1Depression in multiple sclerosis (pre-diagnosis)2.000000e-06
GCST011683_2Low density lipoprotein cholesterol levels7.000000e-08

EFO canonical traits (4, from GWAS)

EFO IDTrait name
EFO:0004530triglyceride measurement
EFO:0004611low density lipoprotein cholesterol measurement
EFO:0004329alcohol drinking
EFO:0004615apolipoprotein B measurement

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

1 total (human), top 1 by PubMed support.

ChemicalActions (top 5)PubMed papers
perfluorooctane sulfonic aciddecreases expression1

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.