TEX52

gene
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Summary

TEX52 (testis expressed 52, HGNC:53643) is a protein-coding gene on chromosome 12p13.33, encoding Testis-expressed protein 52 (A6NCN8).

At a glance

  • MANE Select transcript: NM_001365174

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:53643
Approved symbolTEX52
Nametestis expressed 52
Location12p13.33
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000283297
Ensembl biotypeprotein_coding
Entrez101929469

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000637658

RefSeq mRNA: 2 — MANE Select: NM_001365174 NM_001365174, NM_001365175

CCDS: CCDS91638

Canonical transcript exons

ENST00000637658 — 3 exons

ExonStartEnd
ENSE0000379191028569552857039
ENSE0000379316528548962855446
ENSE0000380001328490462849525

Expression profiles

Bgee: expression breadth ubiquitous, 130 present calls, max score 86.33.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.0148 / max 10.9520, expressed in 3 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1289740.01483

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047386.33gold quality
left testisUBERON:000453374.15gold quality
testisUBERON:000047373.45gold quality
right testisUBERON:000453473.45gold quality
granulocyteCL:000009467.85gold quality
skin of legUBERON:000151166.93gold quality
zone of skinUBERON:000001466.01gold quality
monocyteCL:000057665.46gold quality
leukocyteCL:000073865.13gold quality
body of pancreasUBERON:000115065.04gold quality
right uterine tubeUBERON:000130264.98gold quality
left lobe of thyroid glandUBERON:000112064.78gold quality
skin of abdomenUBERON:000141664.64gold quality
minor salivary glandUBERON:000183064.61gold quality
right lobe of thyroid glandUBERON:000111964.58gold quality
saliva-secreting glandUBERON:000104464.57gold quality
thyroid glandUBERON:000204664.31gold quality
small intestine Peyer’s patchUBERON:000345462.84gold quality
right lobe of liverUBERON:000111462.68gold quality
right adrenal gland cortexUBERON:003582762.66gold quality
cortex of kidneyUBERON:000122562.55gold quality
tonsilUBERON:000237262.31gold quality
spleenUBERON:000210662.25gold quality
small intestineUBERON:000210862.25gold quality
bone marrow cellCL:000209262.23silver quality
duodenumUBERON:000211462.05gold quality
right adrenal glandUBERON:000123361.95gold quality
metanephros cortexUBERON:001053361.76gold quality
stromal cell of endometriumCL:000225561.68gold quality
fundus of stomachUBERON:000116061.58gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.96

Regulation

Is transcription factor: no

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusTex52ENSMUSG00000079304
rattus_norvegicusTex52ENSRNOG00000062735

Protein

Protein identifiers

Testis-expressed protein 52A6NCN8 (reviewed: A6NCN8)

All UniProt accessions (1): A6NCN8

UniProt curated annotations — full annotation on UniProt →

Tissue specificity. Expressed in Testis.

RefSeq proteins (2): NP_001352103, NP_001352104 (=MANE)

Domains & families (InterPro)

IDNameType
IPR029206DUF4532Family

Pfam: PF15046

UniProt features (3 total): chain 1, region of interest 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A6NCN8-F164.460.06

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 2 (showing top): MEF2D_TARGET_GENES, chr12p13

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

74 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TEX52CCDC77Q9BR77542
TEX52LRTM2Q8N967528
TEX52NRIP2Q9BQI9505
TEX52RHNO1Q9BSD3479
TEX52IQSEC3Q9UPP2448
TEX52B4GALNT3Q6L9W6442
TEX52ITFG2Q969R8433
TEX52DCP1BQ8IZD4433
TEX52TSPAN9O75954398
TEX52NINJ2Q9NZG7393
TEX52FBXL14Q8N1E6377
TEX52CACNA2D4Q7Z3S7357
TEX52TULP3O75386354
TEX52SLC6A12P48065321
TEX52ERC1Q8IUD2278

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A2A8T7, A6NCN8, A6NFR6, A6NHR8, B2RW88, O12165, P03331, P18801, P22378, Q0P670, Q0VD86, Q0VF49, Q1LZE2, Q1RMX6, Q32KP7, Q3B8N5, Q3KPS4, Q3SZT6, Q3SZW6, Q3TTI8, Q3ULG3, Q5JTZ5, Q5PR19, Q5R498, Q67926, Q68FQ8, Q6P387, Q6PEX7, Q6ZV65, Q73370, Q75009, Q80VY2, Q86WR6, Q8BII1, Q8C5S3, Q8IYM0, Q8N4L4, Q8N6T0, Q8TAL5, Q8WUB2

Diamond homologs: A6NCN8, Q3TTI8

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

711 predictions. Top by Δscore:

VariantEffectΔscore
12:2854894:A:ACdonor_gain0.9900
12:2854895:C:CCdonor_gain0.9900
12:2854895:CTT:Cdonor_gain0.9900
12:2854897:T:TAdonor_gain0.9900
12:2855036:C:CTacceptor_gain0.9900
12:2855042:C:CTacceptor_gain0.9900
12:2855043:G:Cacceptor_gain0.9900
12:2856951:CTACC:Cdonor_loss0.9900
12:2856952:TACCT:Tdonor_loss0.9900
12:2856953:AC:Adonor_loss0.9900
12:2856954:CCT:Cdonor_loss0.9900
12:2856949:CCCTA:Cdonor_loss0.9800
12:2856950:CCTAC:Cdonor_loss0.9800
12:2856971:T:TAdonor_gain0.9800
12:2854874:C:CAdonor_gain0.9700
12:2855375:CTCG:Cacceptor_gain0.9700
12:2851085:TGA:Tdonor_gain0.9600
12:2855443:CCAT:Cacceptor_gain0.9600
12:2855444:CATC:Cacceptor_gain0.9600
12:2849523:TACCT:Tacceptor_loss0.9400
12:2849525:CCTG:Cacceptor_loss0.9400
12:2849526:C:CGacceptor_loss0.9400
12:2849527:T:Gacceptor_loss0.9400
12:2851020:AG:Adonor_gain0.9400
12:2855379:C:CCacceptor_gain0.9400
12:2855444:CAT:Cacceptor_gain0.9400
12:2855446:TC:Tacceptor_loss0.9400
12:2855448:T:Aacceptor_loss0.9400
12:2855036:C:Tacceptor_gain0.9300
12:2855447:C:CCacceptor_gain0.9300

AlphaMissense

2029 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
12:2855234:A:CF95L0.964
12:2855234:A:TF95L0.964
12:2855236:A:GF95L0.964
12:2855354:G:CF55L0.949
12:2855354:G:TF55L0.949
12:2855356:A:GF55L0.949
12:2854958:A:CS187R0.934
12:2854958:A:TS187R0.934
12:2854960:T:GS187R0.934
12:2855165:G:CS118R0.934
12:2855165:G:TS118R0.934
12:2855167:T:GS118R0.934
12:2855158:A:GW121R0.932
12:2855158:A:TW121R0.932
12:2855039:A:CF160L0.922
12:2855039:A:TF160L0.922
12:2855041:A:GF160L0.922
12:2855060:G:CF153L0.918
12:2855060:G:TF153L0.918
12:2855062:A:GF153L0.918
12:2855227:A:GW98R0.918
12:2855227:A:TW98R0.918
12:2855390:G:CF43L0.907
12:2855390:G:TF43L0.907
12:2855392:A:GF43L0.907
12:2849339:G:CF270L0.902
12:2849339:G:TF270L0.902
12:2849341:A:GF270L0.902
12:2855195:G:CF108L0.899
12:2855195:G:TF108L0.899

dbSNP variants (sampled 300 via entrez): RS1000069714 (12:2851019 T>A), RS1000318680 (12:2850913 T>C), RS1000746033 (12:2854224 C>T), RS1000930747 (12:2849619 C>A), RS1001014559 (12:2852469 C>A,T), RS1001267907 (12:2854356 A>G), RS1001379359 (12:2850676 T>G), RS1001382970 (12:2849368 G>A,T), RS1001422002 (12:2851881 G>A), RS1001429816 (12:2850287 G>A), RS1001681459 (12:2855696 T>C), RS1002363703 (12:2847300 A>G), RS1002381995 (12:2849277 C>T), RS1002477096 (12:2852738 C>G,T), RS1003243990 (12:2857280 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

2 total (human), top 2 by PubMed support.

ChemicalActions (top 5)PubMed papers
aristolochic acid Iincreases expression1
Smokedecreases 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.