TANGO6

gene
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Also known as FLJ12688KIAA1746

Summary

TANGO6 (transport and golgi organization 6 homolog, HGNC:25749) is a protein-coding gene on chromosome 16q22.1, encoding Transport and Golgi organization protein 6 homolog (Q9C0B7). It is a common-essential gene (DepMap: required in 99.7% of cancer cell lines).

Predicted to be involved in protein secretion. Predicted to be located in membrane.

Source: NCBI Gene 79613 — RefSeq curated summary.

At a glance

  • GWAS associations: 5
  • Clinical variants (ClinVar): 176 total
  • Cancer dependency (DepMap): dependent in 99.7% of screened cell lines (common-essential)
  • MANE Select transcript: NM_024562

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:25749
Approved symbolTANGO6
Nametransport and golgi organization 6 homolog
Location16q22.1
Locus typegene with protein product
StatusApproved
AliasesFLJ12688, KIAA1746
Ensembl geneENSG00000103047
Ensembl biotypeprotein_coding
OMIM620188
Entrez79613

Gene structure

Transcript identifiers

Ensembl transcripts: 19 — 10 protein_coding, 4 retained_intron, 3 protein_coding_CDS_not_defined, 2 nonsense_mediated_decay

ENST00000261778, ENST00000561566, ENST00000561856, ENST00000561931, ENST00000562000, ENST00000562491, ENST00000564180, ENST00000565037, ENST00000565852, ENST00000568361, ENST00000883663, ENST00000883664, ENST00000883665, ENST00000883666, ENST00000915345, ENST00000915346, ENST00000953308, ENST00000953309, ENST00000953310

RefSeq mRNA: 1 — MANE Select: NM_024562 NM_024562

CCDS: CCDS45516

Canonical transcript exons

ENST00000261778 — 18 exons

ExonStartEnd
ENSE000006911116892756868928083
ENSE000006911406890921168909402
ENSE000008444116890744368907575
ENSE000009464696893023868930295
ENSE000011116406887515468875290
ENSE000011116436886707968867220
ENSE000011116456908348569085182
ENSE000011116516887811868878280
ENSE000011116526884353168843711
ENSE000034595456902282869022979
ENSE000034793596890232868902504
ENSE000035462966885988468860524
ENSE000035714556897402868974168
ENSE000036158326904030869040421
ENSE000036417916888054868880630
ENSE000036552926886294568863061
ENSE000036573286891908568919219
ENSE000036625006890043468900546

Expression profiles

Bgee: expression breadth ubiquitous, 175 present calls, max score 86.76.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 13.5236 / max 107.9616, expressed in 1798 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
1547918.66601777
1547924.83851586
1547930.01914

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
pancreatic ductal cellCL:000207986.76silver quality
bone marrow cellCL:000209285.36gold quality
tibialis anteriorUBERON:000138585.30silver quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099184.66gold quality
cortical plateUBERON:000534383.35gold quality
calcaneal tendonUBERON:000370182.96gold quality
right lobe of liverUBERON:000111482.69gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047382.43gold quality
ganglionic eminenceUBERON:000402382.16gold quality
ventricular zoneUBERON:000305382.15gold quality
colonic epitheliumUBERON:000039782.09gold quality
gastrocnemiusUBERON:000138881.01gold quality
muscle of legUBERON:000138380.90gold quality
sural nerveUBERON:001548880.51gold quality
ileal mucosaUBERON:000033180.50silver quality
left testisUBERON:000453380.40gold quality
liverUBERON:000210780.26gold quality
hindlimb stylopod muscleUBERON:000425280.14gold quality
right testisUBERON:000453480.00gold quality
stromal cell of endometriumCL:000225579.53gold quality
leukocyteCL:000073879.52gold quality
monocyteCL:000057679.50gold quality
testisUBERON:000047379.11gold quality
prefrontal cortexUBERON:000045178.08gold quality
islet of LangerhansUBERON:000000677.91gold quality
skeletal muscle organUBERON:001489277.52gold quality
popliteal arteryUBERON:000225077.43gold quality
tibial arteryUBERON:000761077.42gold quality
smooth muscle tissueUBERON:000113576.72gold quality
granulocyteCL:000009476.66gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3yes5.47
E-ENAD-17no104.25

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

51 targeting TANGO6, 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-340-5P100.0072.504437
HSA-MIR-4668-3P100.0068.742635
HSA-MIR-453199.9969.703181
HSA-MIR-318599.9968.121959
HSA-MIR-186-5P99.9970.833707
HSA-MIR-4715-3P99.9866.03670
HSA-MIR-426799.9666.532368
HSA-MIR-767-5P99.9570.85993
HSA-MIR-627-3P99.9071.423316
HSA-MIR-153-5P99.8973.866317
HSA-MIR-4659A-3P99.8072.624248
HSA-MIR-4659B-3P99.8072.624248
HSA-MIR-467999.7669.191229
HSA-MIR-3680-3P99.7572.513095
HSA-MIR-4766-5P99.7569.232662
HSA-MIR-5004-5P99.6866.631294
HSA-MIR-3136-3P99.5766.59781
HSA-MIR-7155-3P99.5766.48794
HSA-MIR-1213199.4868.721673
HSA-MIR-942-5P99.4168.401977
HSA-MIR-94099.3766.142064
HSA-MIR-130A-5P99.3370.262623
HSA-MIR-3606-5P99.3169.671168
HSA-MIR-6808-5P99.3166.232150
HSA-MIR-6893-5P99.3166.252119
HSA-MIR-472199.2666.05818
HSA-MIR-10522-5P99.2668.502087
HSA-MIR-3191-5P99.2466.521722
HSA-MIR-6878-3P99.2464.23920
HSA-MIR-6744-3P99.2264.41972

Functional genomics

DepMap (CRISPR cell-line fitness): dependent in 99.7% of screened cell lines, common-essential.

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriotango6ENSDARG00000034001
mus_musculusTango6ENSMUSG00000041949
drosophila_melanogasterTango6FBGN0032728
caenorhabditis_elegansWBGENE00011806

Protein

Protein identifiers

Transport and Golgi organization protein 6 homologQ9C0B7 (reviewed: Q9C0B7)

Alternative names: Transmembrane and coiled-coil domain-containing protein 7

All UniProt accessions (3): Q9C0B7, J3KT80, J3QL82

UniProt curated annotations — full annotation on UniProt →

Subcellular location. Membrane.

Similarity. Belongs to the Tango6 family.

RefSeq proteins (1): NP_078838* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR011989ARM-likeHomologous_superfamily
IPR016024ARM-type_foldHomologous_superfamily
IPR019414Rtp1_C2Domain
IPR019451Rtp1_C1Domain
IPR039600TANGO6/Rtp1Family
IPR057347TANGO6_NDomain
IPR057407HEAT_TANGO6Domain

Pfam: PF10304, PF10363, PF23565, PF25267

UniProt features (9 total): compositionally biased region 3, repeat 2, chain 1, transmembrane region 1, region of interest 1, modified residue 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q9C0B7-F179.250.30

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 (1): 556

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 59 (showing top): GSE18804_SPLEEN_MACROPHAGE_VS_TUMORAL_MACROPHAGE_DN, chr16q22, MONNIER_POSTRADIATION_TUMOR_ESCAPE_UP, RICKMAN_TUMOR_DIFFERENTIATED_WELL_VS_POORLY_DN, GOBP_SECRETION, MODULE_207, XU_GH1_EXOGENOUS_TARGETS_DN, GSE14415_ACT_VS_CTRL_NATURAL_TREG_DN, CIITA_TARGET_GENES, MAFG_TARGET_GENES, SFMBT1_TARGET_GENES, ZNF592_TARGET_GENES, MIR518C_5P, MIR12131, MIR330_5P

GO Biological Process (1): protein secretion (GO:0009306)

GO Molecular Function (0):

GO Cellular Component (1): membrane (GO:0016020)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
protein transport1
secretion by cell1
establishment of protein localization to extracellular region1
protein localization to extracellular region1
cellular anatomical structure1

Protein interactions and networks

STRING

728 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TANGO6MACF1Q9UPN3697
TANGO6MSL1Q68DK7528
TANGO6PRAMEF20Q5VT98488
TANGO6GPN2Q9H9Y4460
TANGO6CEP295NLQ96MC4447
TANGO6SLC7A6OSQ96CW6442
TANGO6SAAL1Q96ER3438
TANGO6TMCO2Q7Z6W1429
TANGO6HEATR4Q86WZ0417
TANGO6PLEKHM3Q6ZWE6402
TANGO6MROH7Q68CQ1397
TANGO6OR51A2Q8NGJ7397
TANGO6ISOC1Q96CN7386
TANGO6FASTKD1Q53R41385
TANGO6RPAP2Q8IXW5365

IntAct

63 interactions, top by confidence:

ABTypeScore
TSSK6HSP90AA1psi-mi:“MI:0914”(association)0.740
POLR2JPOLR2Dpsi-mi:“MI:0914”(association)0.730
DNAJC7PLD2psi-mi:“MI:0914”(association)0.640
POLR2LRCCD1psi-mi:“MI:0914”(association)0.640
MAGEA4MAGEB16psi-mi:“MI:0914”(association)0.530
GPN2POLR2Cpsi-mi:“MI:0914”(association)0.530
DNAJB8DNAJB6psi-mi:“MI:0914”(association)0.530
SLC31A1PRORPpsi-mi:“MI:0914”(association)0.530
TANGO6MACF1psi-mi:“MI:0915”(physical association)0.370
CAPZA2PLEKHG3psi-mi:“MI:0914”(association)0.350
UBE3AIGLC7psi-mi:“MI:0914”(association)0.350
UBE3ATXNL1psi-mi:“MI:0914”(association)0.350
UBE3APOTEFpsi-mi:“MI:0914”(association)0.350
P4HA2CCDC85Cpsi-mi:“MI:0914”(association)0.350
DNAJC7HSPA8psi-mi:“MI:0914”(association)0.350
POLR2BPALM3psi-mi:“MI:0914”(association)0.350
POLR2KBDP1psi-mi:“MI:0914”(association)0.350
RAB18ASDURFpsi-mi:“MI:0914”(association)0.350
RUVBL2ASDURFpsi-mi:“MI:0914”(association)0.350
RUVBL1ASDURFpsi-mi:“MI:0914”(association)0.350
B4GALT2LENG9psi-mi:“MI:0914”(association)0.350
AMZ1IFT56psi-mi:“MI:0914”(association)0.350
ATG7IFT56psi-mi:“MI:0914”(association)0.350
FAM167AIFT56psi-mi:“MI:0914”(association)0.350
TRMUIFT56psi-mi:“MI:0914”(association)0.350
INF2PIPSLpsi-mi:“MI:0914”(association)0.350
HSPA8SBNO1psi-mi:“MI:0914”(association)0.350
AFG2BRCCD1psi-mi:“MI:0914”(association)0.350
PLEKHG7MROH6psi-mi:“MI:0914”(association)0.350
UBXN6ZSWIM8psi-mi:“MI:0914”(association)0.350

BioGRID (79): TANGO6 (Affinity Capture-MS), TANGO6 (Affinity Capture-MS), TANGO6 (Two-hybrid), TANGO6 (Proximity Label-MS), TANGO6 (Affinity Capture-MS), TANGO6 (Affinity Capture-MS), TANGO6 (Affinity Capture-MS), TANGO6 (Affinity Capture-MS), TANGO6 (Affinity Capture-MS), TANGO6 (Affinity Capture-MS), TANGO6 (Affinity Capture-MS), TANGO6 (Affinity Capture-RNA), TANGO6 (Proximity Label-MS), TANGO6 (Synthetic Lethality), TANGO6 (Affinity Capture-MS)

ESM2 similar proteins: A0JML8, A0JP70, A2BID5, A2CEI4, A6NNW6, A9JTS5, E7FAW3, F1QNV4, O75153, O75800, O95248, P0CI65, P56192, P97874, Q08CY4, Q0VC30, Q14689, Q17QN2, Q1LWH4, Q1LXZ7, Q29S07, Q2T9L8, Q32PH0, Q3B7U4, Q3U308, Q3UAW9, Q3UH60, Q3UY23, Q4R4F1, Q641Y9, Q68FL6, Q6DG91, Q6GPP1, Q6PJN8, Q6TEN6, Q6ZNJ1, Q6ZPE2, Q6ZQA0, Q7T006, Q8BWT5

Diamond homologs: Q8C3S2, Q9C0B7

SIGNOR signaling

0 interactions.

Enriched among interaction partners

Reactome pathways and GO biological processes over-represented among this gene’s 105 IntAct physical interaction partners (hypergeometric vs the genome-wide background, BH-FDR, gene-set size 15–500, ranked by fold). A functional readout of the neighbourhood — distinct from this gene’s own memberships above, and biased toward well-studied / hub proteins, so read it as themes rather than proof.

Reactome pathways:

PathwayPartnersFoldFDR
FGFR2 mutant receptor activation671.4×2e-08
Signaling by FGFR2 IIIa TM656.4×4e-08
Abortive elongation of HIV-1 transcript in the absence of Tat646.5×1e-07
Telomere Maintenance846.0×2e-09
PIWI-interacting RNA (piRNA) biogenesis743.1×2e-08
MicroRNA (miRNA) biogenesis642.8×2e-07
Activation of HOX genes during differentiation641.2×2e-07
Signaling by FGFR in disease639.6×3e-07

GO biological processes:

GO termPartnersFoldFDR
protein folding910.1×1e-04

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance142
Likely benign10
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

3847 predictions. Top by Δscore:

VariantEffectΔscore
16:68843709:G:GTdonor_gain1.0000
16:68843709:G:Tdonor_gain1.0000
16:68843710:AGGT:Adonor_loss1.0000
16:68843711:GGTGA:Gdonor_loss1.0000
16:68843712:GTGAG:Gdonor_loss1.0000
16:68843713:T:Gdonor_loss1.0000
16:68843719:G:GTdonor_gain1.0000
16:68862939:TTTTA:Tacceptor_loss1.0000
16:68862940:TTTA:Tacceptor_loss1.0000
16:68862941:TTAG:Tacceptor_loss1.0000
16:68862942:TA:Tacceptor_loss1.0000
16:68863047:G:GTdonor_gain1.0000
16:68863048:G:Tdonor_gain1.0000
16:68863057:CCCAG:Cdonor_loss1.0000
16:68863058:CCAGG:Cdonor_loss1.0000
16:68863059:CAGG:Cdonor_loss1.0000
16:68863060:AGG:Adonor_loss1.0000
16:68863061:GGTAC:Gdonor_loss1.0000
16:68863063:T:Adonor_loss1.0000
16:68875148:T:TAacceptor_gain1.0000
16:68875152:A:AGacceptor_gain1.0000
16:68875152:AGC:Aacceptor_gain1.0000
16:68875152:AGCG:Aacceptor_gain1.0000
16:68875153:G:GCacceptor_gain1.0000
16:68875153:GC:Gacceptor_gain1.0000
16:68875153:GCG:Gacceptor_gain1.0000
16:68875153:GCGG:Gacceptor_gain1.0000
16:68875289:AGGTA:Adonor_loss1.0000
16:68875290:GGTAA:Gdonor_loss1.0000
16:68875291:GT:Gdonor_loss1.0000

AlphaMissense

7097 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
16:68927671:T:CL744P0.993
16:69022914:A:CS977R0.993
16:69022916:C:AS977R0.993
16:69022916:C:GS977R0.993
16:68867124:T:AW300R0.992
16:68867124:T:CW300R0.992
16:69022911:A:CS976R0.991
16:69022913:C:AS976R0.991
16:69022913:C:GS976R0.991
16:68863033:T:CL275P0.989
16:69083570:C:AA1065D0.989
16:69083579:C:AA1068D0.987
16:68867194:T:AV323D0.986
16:68878176:C:AA397D0.986
16:69083569:G:CA1065P0.986
16:69083591:T:CL1072P0.986
16:68863024:T:AV272D0.984
16:68867182:T:AV319D0.983
16:68919193:G:CA701P0.983
16:69022927:T:CL981P0.983
16:69083522:T:CL1049P0.983
16:68878173:T:AV396D0.982
16:68919194:C:AA701D0.981
16:68927661:G:CA741P0.981
16:68927662:C:AA741D0.981
16:68867126:G:CW300C0.979
16:68867126:G:TW300C0.979
16:68878175:G:CA397P0.978
16:68930295:G:AG901R0.978
16:68930295:G:CG901R0.978

dbSNP variants (sampled 300 via entrez): RS1000005278 (16:68971956 T>C), RS1000007416 (16:68991196 A>T), RS1000010981 (16:68968572 T>C,G), RS1000040963 (16:68852932 T>C), RS1000051683 (16:68893304 C>G), RS1000061930 (16:68942222 T>C), RS1000077664 (16:68946277 C>T), RS1000078995 (16:68883175 C>T), RS1000086434 (16:69029553 A>G), RS1000098307 (16:68859849 T>C), RS1000107734 (16:68879356 G>A,C), RS1000113534 (16:69010649 A>C), RS1000122686 (16:68946799 A>T), RS1000134843 (16:69061516 G>A), RS1000156709 (16:69058529 C>T)

Disease associations

OMIM: gene MIM:620188 | disease phenotypes:

GenCC curated gene-disease

Mondo (1): myoepithelial tumor (MONDO:0002380)

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

5 associations (top):

StudyTraitp-value
GCST004030_23Primary sclerosing cholangitis7.000000e-07
GCST005951_13Body mass index5.000000e-11
GCST010241_68Apolipoprotein A1 levels5.000000e-14
GCST010242_316HDL cholesterol levels5.000000e-14
GCST010703_183Brain morphology (MOSTest)5.000000e-11

EFO canonical traits (4, from GWAS)

EFO IDTrait name
EFO:0004340body mass index
EFO:0004614apolipoprotein A 1 measurement
EFO:0004612high density lipoprotein cholesterol measurement
EFO:0004346neuroimaging measurement

MeSH disease descriptors (1)

DescriptorNameTree numbers
D009208MyoepitheliomaC04.557.435.585

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

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

CTD chemical–gene interactions

28 total (human), top 28 by PubMed support.

ChemicalActions (top 5)PubMed papers
Benzo(a)pyreneaffects methylation, decreases expression2
Cadmium Chloridedecreases expression, increases abundance, increases expression2
aristolochic acid Idecreases expression1
GSK-J4decreases expression1
triphenyl phosphateaffects expression1
benzo(e)pyreneincreases methylation1
potassium chromate(VI)affects cotreatment, decreases expression1
gossypol acetic aciddecreases expression1
epigallocatechin gallateaffects cotreatment, decreases expression1
di-n-butylphosphoric acidaffects expression1
perfluorooctane sulfonic aciddecreases expression1
cylindrospermopsinincreases expression1
NSC 689534affects binding, decreases expression1
Resveratrolaffects cotreatment, increases expression1
Leflunomideincreases expression1
Acetaminophendecreases expression1
Cadmiumincreases abundance, increases expression1
Copperaffects binding, decreases expression1
Doxorubicindecreases expression1
Formaldehydedecreases expression1
Methapyrileneincreases methylation1
Plant Extractsaffects cotreatment, increases expression1
Thiramdecreases expression1
Tobacco Smoke Pollutionincreases expression1
Tretinoindecreases expression1
Urethanedecreases expression1
Valproic Acidaffects expression1
7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxidedecreases expression1

Cellosaurus cell lines

1 cell lines: 1 cancer cell line

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

CellosaurusNameCategorySex
CVCL_E1E6Ubigene U-251 MG TANGO6 KOCancer cell lineMale

Clinical trials (associated diseases)

5 trials via MONDO — disease-level, not drug-specific.

TrialPhaseStatusTitle
NCT03600649PHASE1UNKNOWNClinical Trial of SP-2577 (Seclidemstat) in Patients With Relapsed or Refractory Ewing or Ewing-related Sarcomas
NCT05266196PHASE1/PHASE2UNKNOWNA Rollover Protocol to Allow for Continued Access to the LSD1 Inhibitor Seclidemstat (SP-2577)
NCT06239272PHASE1/PHASE2RECRUITINGNRSTS2021, A Risk Adapted Study Evaluating Maintenance Pazopanib, Limited Margin, Dose-Escalated Radiation Therapy and Selinexor in Non-Rhabdomyosarcoma Soft Tissue Sarcoma (NRSTS)
NCT06625190PHASE1/PHASE2RECRUITINGAlpha/Beta T and B Cell Depletion With Zoledronic Acid for Solid Tumors
NCT06244420Not specifiedCOMPLETEDMalignant Myoepithelioma of Bone and Soft Tissues: Diagnostic Imaging and Histology in Relation to Prognosis
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): myoepithelial tumor