TROAP

gene
On this page

Also known as TASTIN

Summary

TROAP (trophinin associated protein, HGNC:12327) is a protein-coding gene on chromosome 12q13.12, encoding Tastin (Q12815). Could be involved with bystin and trophinin in a cell adhesion molecule complex that mediates an initial attachment of the blastocyst to uterine epithelial cells at the time of the embryo implantation. It is a selective cancer dependency (DepMap: 10.3% of cell lines).

Predicted to be involved in cell adhesion. Predicted to be located in cytoplasm.

Source: NCBI Gene 10024 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 141 total
  • Cancer dependency (DepMap): dependent in 10.3% of screened cell lines
  • MANE Select transcript: NM_005480

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:12327
Approved symbolTROAP
Nametrophinin associated protein
Location12q13.12
Locus typegene with protein product
StatusApproved
AliasesTASTIN
Ensembl geneENSG00000135451
Ensembl biotypeprotein_coding
OMIM603872
Entrez10024

Gene structure

Transcript identifiers

Ensembl transcripts: 21 — 15 protein_coding, 4 nonsense_mediated_decay, 2 retained_intron

ENST00000257909, ENST00000380327, ENST00000546735, ENST00000546776, ENST00000547807, ENST00000547923, ENST00000548311, ENST00000548817, ENST00000549275, ENST00000549534, ENST00000549891, ENST00000550346, ENST00000550709, ENST00000551192, ENST00000551245, ENST00000551567, ENST00000879615, ENST00000879616, ENST00000929587, ENST00000929588, ENST00000971667

RefSeq mRNA: 4 — MANE Select: NM_005480 NM_001100620, NM_001278324, NM_001410976, NM_005480

CCDS: CCDS41779, CCDS61117, CCDS8784, CCDS91693

Canonical transcript exons

ENST00000257909 — 15 exons

ExonStartEnd
ENSE000009196114932360449323752
ENSE000009196204932939549329454
ENSE000009196214932985749329991
ENSE000009196224933014549330943
ENSE000009196234933121449331407
ENSE000010602714933157349331731
ENSE000012723724932384549324037
ENSE000023588764932325549323349
ENSE000035164584932720949327330
ENSE000035458894932666849326720
ENSE000035484364932574749325884
ENSE000035700934932916149329244
ENSE000036304514932550149325658
ENSE000036329364932607649326158
ENSE000036889304932892749329055

Expression profiles

Bgee: expression breadth ubiquitous, 181 present calls, max score 97.32.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 29.2893 / max 274.8085, expressed in 1481 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
12532327.91151456
1253250.6988330
1253240.6789463

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
oocyteCL:000002397.32gold quality
secondary oocyteCL:000065595.99gold quality
ventricular zoneUBERON:000305395.44gold quality
ganglionic eminenceUBERON:000402391.00gold quality
left testisUBERON:000453389.15gold quality
right testisUBERON:000453488.80gold quality
embryoUBERON:000092288.61gold quality
lower esophagus mucosaUBERON:003583486.87gold quality
testisUBERON:000047386.79gold quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099186.74gold quality
mucosa of transverse colonUBERON:000499186.58gold quality
endometrium epitheliumUBERON:000481184.27silver quality
bone marrowUBERON:000237182.59gold quality
bone marrow cellCL:000209282.35gold quality
esophagus mucosaUBERON:000246982.28gold quality
rectumUBERON:000105280.24gold quality
stromal cell of endometriumCL:000225580.11gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047379.60gold quality
spermCL:000001978.76silver quality
trabecular bone tissueUBERON:000248378.55gold quality
male germ cellCL:000001578.05silver quality
ileal mucosaUBERON:000033176.85silver quality
vermiform appendixUBERON:000115476.80gold quality
lymph nodeUBERON:000002976.74gold quality
caecumUBERON:000115375.56gold quality
thymusUBERON:000237075.32silver quality
transverse colonUBERON:000115774.40gold quality
duodenumUBERON:000211474.15gold quality
gingival epitheliumUBERON:000194973.94gold quality
skin of abdomenUBERON:000141673.55gold quality

Single-cell (SCXA)

Detected in 4 experiment(s), a significant marker in 3.

ExperimentMarker?Max mean expression
E-GEOD-99795yes233.68
E-MTAB-6678yes7.64
E-ANND-3yes5.03
E-MTAB-6142no364.30

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

10 targeting TROAP, 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-6721-5P99.9368.922981
HSA-MIR-95-5P99.8972.173973
HSA-MIR-5004-5P99.6866.631294
HSA-MIR-1207-5P99.4969.112983
HSA-MIR-1224-5P99.4865.59803
HSA-MIR-391599.4568.491905
HSA-MIR-4763-3P99.1067.832649
HSA-MIR-468996.9765.791209
HSA-MIR-664B-5P96.7467.50509
HSA-MIR-6858-5P96.0564.591020

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 10.3% of screened cell lines.

Literature-anchored findings (GeneRIF, showing 12)

  • plays an important role in mammalian cells by associating with the microtubular cytoskeleton (PMID:12049630)
  • the major function of tastin during mitosis is to maintain the structural and dynamic features of centrosomes, thereby contributing to spindle bipolarity. (PMID:18218922)
  • these results indicate that TROAP suppresses cellular growth and migration in hepatocellular carcinoma (PMID:29117881)
  • the present study provided evidence that TROAP serves a role in GC cells by promoting cell proliferation, cell cycle progression and invasion in vitro. Combined analysis of cell lines and datasets from a public database, demonstrated that TROAP overexpression may be used as a predictor of poor survival in patients with GC. (PMID:29956806)
  • Elevated TROAP expression is an independent predictor of poor survival in liver cancer. (PMID:30284652)
  • Study found that TROAP expression correlates with patient survival and speculated that it may be involved in prostate cancer progression. (PMID:30431120)
  • The present study suggests that TROAP plays an important role in promoting the proliferation, invasion, and metastasis of breast cancer. (PMID:31198787)
  • TROAP switches DYRK1 activity to drive hepatocellular carcinoma progression. (PMID:33500384)
  • MiR-532-3p suppresses cell viability, migration and invasion of clear cell renal cell carcinoma through targeting TROAP. (PMID:34287099)
  • Tastin promotes non-small-cell lung cancer progression through the ErbB4, PI3K/AKT, and ERK1/2 pathways. (PMID:36691332)
  • TROAP Promotes the Proliferation, Migration, and Metastasis of Kidney Renal Clear Cell Carcinoma with the Help of STAT3. (PMID:37298609)
  • METTL3 regulatory TROAP can regulate the progression of non-small cell lung cancer through PI3K/AKT and EMT signaling pathway. (PMID:37608033)

Cross-species orthologs

3 orthologs

OrganismSymbolGene ID
danio_reriotroapENSDARG00000094977
mus_musculusTroapENSMUSG00000032783
rattus_norvegicusTroapENSRNOG00000060703

Protein

Protein identifiers

TastinQ12815 (reviewed: Q12815)

Alternative names: Trophinin-assisting protein, Trophinin-associated protein

All UniProt accessions (11): B7Z5Q9, Q12815, F8VR46, F8VVS4, F8VVT5, F8VVX4, F8VXF3, F8VXV6, F8W052, F8W130, F8W1E3

UniProt curated annotations — full annotation on UniProt →

Function. Could be involved with bystin and trophinin in a cell adhesion molecule complex that mediates an initial attachment of the blastocyst to uterine epithelial cells at the time of the embryo implantation.

Subunit / interactions. Directly binds bystin, and indirectly trophinin.

Subcellular location. Cytoplasm.

Tissue specificity. Strong expression at implantation sites. Was exclusively localized to the apical side of the syncytiotrophoblast. Also found in macrophages.

Isoforms (3)

UniProt IDNamesCanonical?
Q12815-11yes
Q12815-22
Q12815-33

RefSeq proteins (4): NP_001094090, NP_001265253, NP_001397905, NP_005471* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR026133TastinFamily

UniProt features (29 total): modified residue 9, region of interest 6, compositionally biased region 5, repeat 4, splice variant 3, chain 1, sequence conflict 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q12815-F146.870.00

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Post-translational modifications (9): 16, 98, 170, 324, 334, 344, 362, 363, 376

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 160 (showing top): HORIUCHI_WTAP_TARGETS_DN, ENK_UV_RESPONSE_KERATINOCYTE_UP, IVANOVA_HEMATOPOIESIS_LATE_PROGENITOR, PATIL_LIVER_CANCER, PUJANA_CHEK2_PCC_NETWORK, MODULE_118, KRASNOSELSKAYA_ILF3_TARGETS_DN, MODULE_120, FISCHER_G2_M_CELL_CYCLE, HELLER_HDAC_TARGETS_SILENCED_BY_METHYLATION_UP, SPIELMAN_LYMPHOBLAST_EUROPEAN_VS_ASIAN_UP, FISCHER_DREAM_TARGETS, SHEN_SMARCA2_TARGETS_DN, NUYTTEN_EZH2_TARGETS_DN, GEORGES_TARGETS_OF_MIR192_AND_MIR215

GO Biological Process (1): cell adhesion (GO:0007155)

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (1): cytoplasm (GO:0005737)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
cellular process1
binding1
intracellular anatomical structure1
cellular anatomical structure1

Protein interactions and networks

STRING

1196 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TROAPTROQ12816999
TROAPBYSLQ13895998
TROAPFAM117BQ6P1L5607
TROAPRPS6P08227546
TROAPKIF4AO95239527
TROAPRNF169Q8NCN4517
TROAPDRC5Q5JU00515
TROAPDYNLT1P63172508
TROAPTICRRQ7Z2Z1501
TROAPDZANK1Q9NVP4475
TROAPRAD54L2Q9Y4B4474
TROAPMELKQ14680436
TROAPVTNP01141435
TROAPTOP2AP11388432
TROAPHJURPQ8NCD3429

IntAct

120 interactions, top by confidence:

ABTypeScore
TROAPMAPRE1psi-mi:“MI:0915”(physical association)0.850
MAPRE1TROAPpsi-mi:“MI:0915”(physical association)0.850
TROAPMAPRE3psi-mi:“MI:0915”(physical association)0.830
TROAPDYRK1Bpsi-mi:“MI:0915”(physical association)0.790
DYRK1BTROAPpsi-mi:“MI:0915”(physical association)0.790
DCAF7DIAPH1psi-mi:“MI:0914”(association)0.730
TRIM23TROAPpsi-mi:“MI:0915”(physical association)0.700
TROAPTRIM23psi-mi:“MI:0915”(physical association)0.700
TRAF2TROAPpsi-mi:“MI:0915”(physical association)0.670
BANPTROAPpsi-mi:“MI:0915”(physical association)0.670
TROAPBANPpsi-mi:“MI:0915”(physical association)0.670
TROAPTRAF2psi-mi:“MI:0915”(physical association)0.670
TROAPDYRK1Apsi-mi:“MI:0915”(physical association)0.670

BioGRID (105): TROAP (Two-hybrid), TROAP (Two-hybrid), TROAP (Two-hybrid), MAPRE1 (Two-hybrid), MAPRE3 (Two-hybrid), BANP (Two-hybrid), KRT40 (Two-hybrid), TROAP (Affinity Capture-MS), TROAP (Affinity Capture-MS), TROAP (Proximity Label-MS), TROAP (Proximity Label-MS), MAPRE3 (Two-hybrid), TROAP (Affinity Capture-MS), TROAP (Affinity Capture-MS), TROAP (Affinity Capture-MS)

ESM2 similar proteins: A0A096MK47, A0A1D5RMD1, A2AQH4, A6NCI8, A8MUA0, A8MX80, B2RRE4, B7ZNG4, E9Q3S4, O15027, O94854, P70670, Q0GGX2, Q12802, Q12815, Q3URK3, Q3V0A6, Q5DTT3, Q5F2C3, Q5FW52, Q5H9F3, Q5SW25, Q5SWP3, Q5VV67, Q5VWP3, Q5VYM1, Q66HG9, Q69ZZ9, Q6NXZ1, Q6NZN1, Q6P1W5, Q711Q0, Q7TSG5, Q7Z434, Q86TB3, Q8K4E0, Q8N5Q1, Q8N9G6, Q8NFU7, Q8VCF0

Diamond homologs: B7ZNG4, Q12815

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance112
Likely benign12
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

2388 predictions. Top by Δscore:

VariantEffectΔscore
12:49323602:A:AGacceptor_gain1.0000
12:49323603:G:GGacceptor_gain1.0000
12:49323751:GG:Gdonor_gain1.0000
12:49323752:GG:Gdonor_gain1.0000
12:49326068:T:TAacceptor_gain1.0000
12:49327329:GG:Gdonor_gain1.0000
12:49327330:GG:Gdonor_gain1.0000
12:49323590:C:CAacceptor_gain0.9900
12:49323596:A:AGacceptor_gain0.9900
12:49323597:A:Gacceptor_gain0.9900
12:49323603:GCC:Gacceptor_gain0.9900
12:49323603:GCCAT:Gacceptor_gain0.9900
12:49323749:AAGGG:Adonor_loss0.9900
12:49323750:AGGG:Adonor_loss0.9900
12:49323751:GGGTA:Gdonor_loss0.9900
12:49323753:G:GGdonor_gain0.9900
12:49323754:T:Adonor_loss0.9900
12:49323977:G:GTdonor_gain0.9900
12:49324327:G:GTdonor_gain0.9900
12:49325499:A:AGacceptor_gain0.9900
12:49325500:G:GGacceptor_gain0.9900
12:49325627:G:GTdonor_gain0.9900
12:49325745:AG:Aacceptor_gain0.9900
12:49325746:GG:Gacceptor_gain0.9900
12:49325746:GGGT:Gacceptor_gain0.9900
12:49326060:T:TAacceptor_gain0.9900
12:49326069:G:Aacceptor_gain0.9900
12:49327207:A:AGacceptor_gain0.9900
12:49327208:G:GGacceptor_gain0.9900
12:49327208:GCT:Gacceptor_gain0.9900

AlphaMissense

4916 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
12:49325521:T:CF120L0.996
12:49325523:T:AF120L0.996
12:49325523:T:GF120L0.996
12:49325522:T:CF120S0.989
12:49325555:T:CL131P0.988
12:49330167:T:CL441P0.988
12:49330158:T:CL438P0.986
12:49329878:T:CF396L0.985
12:49329880:T:AF396L0.985
12:49329880:T:GF396L0.985
12:49330170:T:CL442S0.985
12:49325552:T:CI130T0.983
12:49325522:T:GF120C0.982
12:49325543:T:CL127P0.982
12:49325552:T:AI130N0.982
12:49329452:T:AW388R0.981
12:49329452:T:CW388R0.981
12:49325557:T:CS132P0.978
12:49325545:G:CA128P0.977
12:49329454:G:CW388C0.977
12:49329454:G:TW388C0.977
12:49325552:T:GI130S0.976
12:49329876:T:CL395S0.976
12:49323673:T:CI22T0.974
12:49330146:G:CR434P0.974
12:49331576:T:CF766L0.974
12:49331578:C:AF766L0.974
12:49331578:C:GF766L0.974
12:49325555:T:AL131Q0.973
12:49325819:T:CF190L0.969

dbSNP variants (sampled 300 via entrez): RS1000031222 (12:49322567 A>C,T), RS1000532449 (12:49325941 A>C,G), RS1000857762 (12:49330912 C>G), RS1001064652 (12:49324236 A>G), RS1001095693 (12:49331188 C>T), RS1002036672 (12:49325943 G>C), RS1002096980 (12:49331840 G>A,C,T), RS1002640365 (12:49322639 G>A), RS1002978438 (12:49322157 A>C,G), RS1003147419 (12:49325692 G>A,T), RS1003446979 (12:49327754 A>C,G), RS1003495029 (12:49322117 G>A,C,T), RS1003570332 (12:49323508 G>A,C), RS1003588727 (12:49321805 C>T), RS1003924160 (12:49328437 G>A)

Disease associations

OMIM: gene MIM:603872 | 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

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

ChemicalActions (top 5)PubMed papers
sodium arsenitedecreases expression, increases abundance, increases expression4
Tretinoindecreases expression3
Valproic Acidaffects cotreatment, decreases expression3
Arsenicaffects methylation, increases abundance, increases expression2
Tobacco Smoke Pollutiondecreases expression2
FR900359decreases phosphorylation1
bisphenol Faffects cotreatment, decreases expression1
propionaldehydedecreases expression1
bisphenol Adecreases expression1
beta-lapachonedecreases expression1
cobaltous chloridedecreases expression1
butyraldehydedecreases expression1
perfluorooctanoic aciddecreases expression1
zinc chromatedecreases expression, increases abundance1
aflatoxin B2decreases methylation1
diallyl trisulfidedecreases expression1
tamibarotenedecreases expression1
chromium hexavalent iondecreases expression, increases abundance1
perfluoro-n-nonanoic aciddecreases expression1
2-palmitoylglycerolincreases expression1
4-(5-benzo(1,3)dioxol-5-yl-4-pyridin-2-yl-1H-imidazol-2-yl)benzamideaffects cotreatment, decreases expression1
ICG 001decreases expression1
abrineincreases expression1
palbociclibdecreases expression1
dorsomorphinaffects cotreatment, decreases expression1
jinfukangincreases expression1
(+)-JQ1 compounddecreases expression1
NSC668394decreases expression1
Resveratrolaffects cotreatment, increases expression1
Temozolomideincreases expression1

Cellosaurus cell lines

1 cell lines: 1 transformed cell line

First 10 cell lines (id-ordered, not curated):

CellosaurusNameCategorySex
CVCL_B3K8Abcam HEK293T TROAP KOTransformed cell lineFemale

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.