TEX19

gene
On this page

Also known as FLJ35767

Summary

TEX19 (testis expressed 19, HGNC:33802) is a protein-coding gene on chromosome 17q25.3, encoding Testis-expressed protein 19 (Q8NA77). Required during spermatogenesis and placenta development, participating in the repression of retrotransposable elements and prevent their mobilization.

Predicted to enable piRNA binding activity. Involved in transposable element silencing. Predicted to be active in cytoplasm and nucleus.

Source: NCBI Gene 400629 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 16 total
  • MANE Select transcript: NM_207459

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:33802
Approved symbolTEX19
Nametestis expressed 19
Location17q25.3
Locus typegene with protein product
StatusApproved
AliasesFLJ35767
Ensembl geneENSG00000182459
Ensembl biotypeprotein_coding
OMIM615647
Entrez400629

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000333437

RefSeq mRNA: 1 — MANE Select: NM_207459 NM_207459

CCDS: CCDS11809

Canonical transcript exons

ENST00000333437 — 2 exons

ExonStartEnd
ENSE000012908758236188082363775
ENSE000013301508235924782359285

Expression profiles

Bgee: expression breadth broad, 21 present calls, max score 93.63.

FANTOM5 (CAGE): breadth tissue_specific, TPM avg 0.7286 / max 237.3907, expressed in 148 samples.

FANTOM5 promoters (1 alternative TSS)

Promoter IDTPM avgSamples expressed
1635020.7286148

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
secondary oocyteCL:000065593.63gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047393.35gold quality
right testisUBERON:000453490.16gold quality
oocyteCL:000002389.18gold quality
left testisUBERON:000453387.44gold quality
testisUBERON:000047385.00gold quality
tibialis anteriorUBERON:000138570.61silver quality
adult organismUBERON:000702369.79gold quality
epithelial cell of pancreasCL:000008366.76gold quality
pancreatic ductal cellCL:000207963.94silver quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099163.54gold quality
amniotic fluidUBERON:000017360.78gold quality
ileal mucosaUBERON:000033159.25gold quality
buccal mucosa cellCL:000233658.03gold quality
deltoidUBERON:000147657.84gold quality
skin of hipUBERON:000155456.47silver quality
endothelial cellCL:000011554.64gold quality
cardiac muscle of right atriumUBERON:000337954.34gold quality
left ventricle myocardiumUBERON:000656654.23gold quality
kidney epitheliumUBERON:000481953.93gold quality
upper arm skinUBERON:000426353.52gold quality
upper leg skinUBERON:000426250.92silver quality
myocardiumUBERON:000234950.25gold quality
quadriceps femorisUBERON:000137749.75gold quality
vastus lateralisUBERON:000137947.55gold quality
nasal cavity epitheliumUBERON:000538447.03gold quality
layer of synovial tissueUBERON:000761645.32gold quality
muscle tissueUBERON:000238544.05gold quality
skeletal muscle tissueUBERON:000113443.57gold quality
skeletal muscle tissue of rectus abdominisUBERON:000451143.37gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-GEOD-124263yes1321.38
E-ANND-3no1.48

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

52 targeting TEX19, 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-426799.9666.532368
HSA-MIR-548AJ-3P99.9673.385345
HSA-MIR-548X-3P99.9673.385345
HSA-MIR-548J-3P99.9472.614881
HSA-MIR-548AE-3P99.9372.664867
HSA-MIR-548AH-3P99.9372.544872
HSA-MIR-548AM-3P99.9372.544872
HSA-MIR-548AQ-3P99.9372.664867
HSA-MIR-497-5P99.9271.832674
HSA-MIR-15B-5P99.9072.782798
HSA-MIR-15A-5P99.9072.802787
HSA-MIR-16-5P99.9072.802780
HSA-MIR-195-5P99.9072.812805
HSA-MIR-424-5P99.8971.902641
HSA-MIR-6838-5P99.8971.942690
HSA-MIR-548D-3P99.8770.674362
HSA-MIR-548BB-3P99.8670.584354
HSA-MIR-221-5P99.8665.451052
HSA-MIR-807399.8665.211118
HSA-MIR-548AC99.8470.774351
HSA-MIR-548H-3P99.8470.804349
HSA-MIR-548Z99.8470.804349
HSA-MIR-431999.7669.832586
HSA-MIR-182599.7268.111089
HSA-MIR-453099.6966.471509
HSA-MIR-10394-5P99.6566.831852
HSA-MIR-120599.6566.761826
HSA-MIR-613299.6065.831554
HSA-MIR-6836-5P99.6065.621538
HSA-MIR-4649-3P99.5666.901783

Literature-anchored findings (GeneRIF, showing 6)

  • Tex19 is a mammalian-specific protein duplicated in mouse and rat, renamed Tex19.1 and Tex19.2, whereas only one form is found in human. (PMID:18096721)
  • TEX19 is a target gene of the BACH1 transcription factor according to ChIP-seq analysis in HEK 293 cells. (PMID:21555518)
  • TEX19 expression in normal tissue is restricted to human testis. TEX19 mRNA expression was detected in 60 % of bladder cancer samples, whereas 58.20 % were positive for TEXT19 protein expression. Compared to low-grade tumors, TEX19 exhibited increased expression in high-grade tumors, from 53.69 to 77.14 %, respectively. TEX19 was also expressed in all six bladder cancer cell lines. (PMID:26695143)
  • TEX19 is required to drive cell proliferation in a range of cancer cell types, possibly mediated via an oncogenic transcript regulation mechanism. TEX19 expression is linked to a poor prognosis for some cancers and collectively these findings indicate that not only can TEX19 expression serve as a novel cancer biomarker (PMID:28446200)
  • High TEX19 expression is associated with ovarian carcinoma progression. (PMID:31843525)
  • In silico modeling of the interaction between TEX19 and LIRE1, and analysis of TEX19 gene missense SNPs. (PMID:34036740)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
mus_musculusTex19.1ENSMUSG00000039329
mus_musculusTex19.2ENSMUSG00000039337
rattus_norvegicusTex19.1ENSRNOG00000036670
rattus_norvegicusTex19.2ENSRNOG00000036671

Protein

Protein identifiers

Testis-expressed protein 19Q8NA77 (reviewed: Q8NA77)

All UniProt accessions (1): Q8NA77

UniProt curated annotations — full annotation on UniProt →

Function. Required during spermatogenesis and placenta development, participating in the repression of retrotransposable elements and prevent their mobilization. Collaborates with the Piwi-interacting RNA (piRNA) pathway, which mediates the repression of transposable elements during meiosis by forming complexes composed of piRNAs and Piwi proteins. Interacts with Piwi proteins and directly binds piRNAs, a class of 24 to 30 nucleotide RNAs that are generated by a Dicer-independent mechanism and are primarily derived from transposons and other repeated sequence elements. Also during spermatogenesis, promotes, with UBR2, SPO11-dependent recombination foci to accumulate and drive robust homologous chromosome synapsis. Interacts with LINE-1 retrotransposon encoded LIRE1, stimulates LIRE1 polyubiquitination, mediated by UBR2, and degradation, inhibiting LINE-1 retrotransposon mobilization.

Subunit / interactions. Interacts with UBR2; does not lead to TEX19 degradation and stabilizes it. Interacts with piRNA-associated proteins DDX4, EDC4, MAEL, PIWIL1, PIWIL2, RANBP9 and TDRD6. Interacts with L1RE1.

Subcellular location. Cytoplasm.

Tissue specificity. Expressed in testis. Expressed in undifferentiated embryonic stem cells.

Induction. Down-regulated by gonadotropin suppression sufficient to cause marked suppression of spermatogenesis and additionally progestogen treatment.

RefSeq proteins (1): NP_997342* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR029093TEX19Family

Pfam: PF15553

UniProt features (5 total): region of interest 3, chain 1, compositionally biased region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8NA77-F157.400.00

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 81 (showing top): AP1_01, GOBP_MALE_GAMETE_GENERATION, GOBP_ORGANELLE_FISSION, GOBP_REPRODUCTIVE_SYSTEM_DEVELOPMENT, TGANTCA_AP1_C, GARCIA_TARGETS_OF_FLI1_AND_DAX1_DN, NRF2_Q4, GOBP_SEX_DIFFERENTIATION, GOBP_DEVELOPMENTAL_PROCESS_INVOLVED_IN_REPRODUCTION, GOBP_MEIOTIC_CELL_CYCLE_PROCESS, GOBP_PLACENTA_DEVELOPMENT, NIKOLSKY_BREAST_CANCER_17Q21_Q25_AMPLICON, NFE2_01, GOBP_MALE_SEX_DIFFERENTIATION, GOBP_DEVELOPMENT_OF_PRIMARY_SEXUAL_CHARACTERISTICS

GO Biological Process (8): placenta development (GO:0001890), reciprocal meiotic recombination (GO:0007131), male meiotic nuclear division (GO:0007140), spermatogenesis (GO:0007283), male gonad development (GO:0008584), transposable element silencing (GO:0010526), cell differentiation (GO:0030154), meiotic cell cycle (GO:0051321)

GO Molecular Function (2): piRNA binding (GO:0034584), protein binding (GO:0005515)

GO Cellular Component (2): nucleus (GO:0005634), cytoplasm (GO:0005737)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
male gamete generation2
meiotic nuclear division2
animal organ development1
meiosis I1
reciprocal homologous recombination1
meiotic cell cycle process1
meiotic cell cycle1
developmental process involved in reproduction1
gonad development1
development of primary male sexual characteristics1
negative regulation of gene expression1
retrotransposition1
cellular developmental process1
cell cycle1
sexual reproduction1
reproductive process1
regulatory RNA binding1
binding1
intracellular membrane-bounded organelle1
intracellular anatomical structure1
cellular anatomical structure1

Protein interactions and networks

STRING

452 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TEX19TEX48A0A1B0GUV7571
TEX19SECTM1Q8WVN6462
TEX19TEX9Q8N6V9447
TEX19UTS2RQ9UKP6438
TEX19TEX22C9J3V5433
TEX19TEX11Q8IYF3426
TEX19SYCP1Q15431421
TEX19C5orf47Q569G3419
TEX19RAD21L1Q9H4I0417
TEX19HORMAD1Q86X24415
TEX19SMC1BQ8NDV3408
TEX19KRT33BQ14525403
TEX19CCDC185Q8N715402
TEX19ZNF664Q8N3J9398
TEX19TEX26Q8N6G2398

IntAct

26 interactions, top by confidence:

ABTypeScore
TEX19ZNF490psi-mi:“MI:0915”(physical association)0.560
ZNF648TEX19psi-mi:“MI:0915”(physical association)0.560
GRNTEX19psi-mi:“MI:0915”(physical association)0.560
TEX19WFS1psi-mi:“MI:0915”(physical association)0.560
TEX19KIF1Bpsi-mi:“MI:0915”(physical association)0.560
TEX19RNF11psi-mi:“MI:0915”(physical association)0.560
ATXN3TEX19psi-mi:“MI:0915”(physical association)0.560
TEX19ZNF316psi-mi:“MI:0914”(association)0.350
TEX19FYNpsi-mi:“MI:0914”(association)0.350
TRIM63TEX19psi-mi:“MI:0915”(physical association)0.000
TRIM55TEX19psi-mi:“MI:0915”(physical association)0.000
ZNF490TEX19psi-mi:“MI:0915”(physical association)0.000
ZNF648TEX19psi-mi:“MI:0915”(physical association)0.000

BioGRID (53): TEX19 (Two-hybrid), ZNF490 (Two-hybrid), TEX19 (Affinity Capture-MS), TEX19 (Two-hybrid), TEX19 (Two-hybrid), TEX19 (Negative Genetic), UBB (Affinity Capture-MS), TRPT1 (Affinity Capture-MS), ZNF561 (Affinity Capture-MS), RREB1 (Affinity Capture-MS), RCOR1 (Affinity Capture-MS), SALL1 (Affinity Capture-MS), SALL2 (Affinity Capture-MS), ZNF195 (Affinity Capture-MS), TRIP6 (Affinity Capture-MS)

ESM2 similar proteins: A0A1L8I316, A0A1W2PR82, A0A286YDK6, A5PJD3, A6H7B4, A6NEV1, A6NGY1, A6NHS1, A6QP24, A8MUA0, A8MUI8, A8MV72, A8MX80, A8MYA2, D3ZAQ5, O60393, P0C1T1, P0DL12, P43359, Q0KK55, Q0VD86, Q1RN00, Q32LI3, Q3UN58, Q3ZCQ2, Q5M831, Q5M844, Q66H53, Q68US1, Q6AYA8, Q6DIA7, Q6K1E7, Q6PE65, Q6ZW13, Q80VY2, Q8BII1, Q8IY42, Q8N9G6, Q8NA77, Q8TDR4

Diamond homologs: Q5XHY3, Q8NA77, Q99MV2, Q9D5S1

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance15
Likely benign0
Benign1

Top pathogenic / likely-pathogenic (0)

SpliceAI

180 predictions. Top by Δscore:

VariantEffectΔscore
17:82361875:TCCA:Tacceptor_loss1.0000
17:82361877:CAG:Cacceptor_loss1.0000
17:82361878:A:AGacceptor_gain1.0000
17:82361878:AG:Aacceptor_loss1.0000
17:82361879:G:GCacceptor_gain1.0000
17:82361879:GC:Gacceptor_gain1.0000
17:82361879:GCT:Gacceptor_gain1.0000
17:82361879:GCTC:Gacceptor_gain1.0000
17:82361879:GCTCT:Gacceptor_gain1.0000
17:82359281:GGATG:Gdonor_gain0.9800
17:82359282:G:GTdonor_gain0.9800
17:82359283:A:Tdonor_gain0.9800
17:82361869:T:TAacceptor_gain0.9800
17:82359315:G:GTdonor_gain0.9600
17:82361875:TCCAG:Tacceptor_gain0.9500
17:82361876:CCAGC:Cacceptor_gain0.9500
17:82359301:G:GTdonor_gain0.9400
17:82361877:CAGC:Cacceptor_gain0.9300
17:82361878:AGCTC:Aacceptor_gain0.9300
17:82359283:ATGGT:Adonor_loss0.9100
17:82359286:G:Cdonor_loss0.9100
17:82359286:G:GGdonor_gain0.9100
17:82359287:T:Cdonor_loss0.9100
17:82359288:GAGA:Gdonor_loss0.9000
17:82359282:GATG:Gdonor_gain0.8900
17:82359290:G:Cdonor_loss0.8900
17:82361879:G:Tacceptor_gain0.8900
17:82361877:CA:Cacceptor_gain0.8800
17:82359342:CTGG:Cdonor_gain0.8700
17:82361878:A:Cacceptor_gain0.8600

AlphaMissense

1073 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
17:82362253:T:CF35L0.973
17:82362255:C:AF35L0.973
17:82362255:C:GF35L0.973
17:82362211:T:AW21R0.968
17:82362211:T:CW21R0.968
17:82362250:T:CC34R0.966
17:82362252:C:GC34W0.966
17:82362213:G:CW21C0.963
17:82362213:G:TW21C0.963
17:82362259:T:CC37R0.956
17:82362261:C:GC37W0.956
17:82362263:T:CF38S0.946
17:82362274:T:CF42L0.946
17:82362276:T:AF42L0.946
17:82362276:T:GF42L0.946
17:82362262:T:CF38L0.945
17:82362264:C:AF38L0.945
17:82362264:C:GF38L0.945
17:82362573:G:CW141C0.942
17:82362573:G:TW141C0.942
17:82362254:T:CF35S0.940
17:82362260:G:AC37Y0.939
17:82362251:G:AC34Y0.934
17:82362254:T:GF35C0.932
17:82362250:T:AC34S0.929
17:82362251:G:CC34S0.929
17:82362154:T:CC2R0.928
17:82362260:G:TC37F0.927
17:82362259:T:AC37S0.926
17:82362260:G:CC37S0.926

dbSNP variants (sampled 300 via entrez): RS1000205848 (17:82358780 TAG>T), RS1000249427 (17:82364081 T>C), RS1000392760 (17:82361968 C>T), RS1002003581 (17:82361575 T>A,C), RS1002380841 (17:82359369 G>A,C), RS1002646936 (17:82358020 C>A,G,T), RS1004052278 (17:82359024 C>A,T), RS1006299596 (17:82363318 G>A), RS1006748778 (17:82363811 G>T), RS1006779632 (17:82364195 C>T), RS1007570703 (17:82363389 A>G), RS1008654121 (17:82357291 G>A), RS1009011494 (17:82359943 C>A,T), RS1010270964 (17:82363733 A>G), RS1010897110 (17:82362813 C>G)

Disease associations

OMIM: gene MIM:615647 | 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

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

ChemicalActions (top 5)PubMed papers
Valproic Acidaffects expression, increases expression, increases methylation3
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression, affects cotreatment2
Benzo(a)pyreneaffects methylation, increases expression, increases methylation2
Silverincreases expression2
Cadmium Chlorideincreases abundance, increases expression2
p-Chloromercuribenzoic Acidaffects cotreatment, increases expression2
aristolochic acid Iincreases expression1
testosterone enanthateaffects cotreatment, decreases expression1
propionaldehydeincreases expression1
bisphenol Aincreases expression1
trichostatin Aincreases expression1
2-butenalincreases expression1
tris(1,3-dichloro-2-propyl)phosphateaffects expression1
sodium arseniteincreases expression1
butyraldehydeincreases expression1
9,10-dihydro-9,10-dihydroxybenzo(a)pyreneincreases expression1
mercuric bromideaffects cotreatment, increases expression1
gallium arsenideincreases expression1
pentanalincreases expression1
cetrorelixaffects cotreatment, decreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideincreases expression, affects cotreatment1
dorsomorphinaffects cotreatment, increases expression1
NSC 689534affects binding, increases expression1
NSC668394increases expression1
Temozolomideincreases expression1
Leflunomideincreases expression1
Aldehydesincreases expression1
Atrazineincreases expression1
Cadmiumincreases abundance, increases expression1
Copperaffects binding, increases 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.