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WormBase Tree Display for Gene: WBGene00006565

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Name Class

WBGene00006565EvidenceCGC_data_submission
SMapS_parentSequenceY63D3A
IdentityVersion1
NameCGC_nametfg-1
Sequence_nameY63D3A.5
Molecular_nameY63D3A.5
Y63D3A.5.1
CE20336
Y63D3A.5.2
Other_nameCELE_Y63D3A.5Accession_evidenceNDBBX284601
Public_nametfg-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:41WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtfg
Allele (65)
StrainWBStrain00037094
RNASeq_FPKM (74)
GO_annotation00098434
00098435
00098436
00098437
00098438
00098439
00098440
00098441
00098442
00098443
00098444
00098445
00098446
00098447
00098448
00098449
00098450
00098451
00098452
00098453
00098454
00098455
00098456
00114353
00114354
00114355
Ortholog (21)
ParalogWBGene00013507Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptiontfg-1 encodes a tumor suppressor gene homologous to human TRK-fused gene (TFG)(OMIM: 602498); TFG-1 is sufficient and necessary to inhibit the normal apoptotic pathway; TFG-1 influences body size and responsible for determining the size of adults; TFG-1 functions in a novel pathway independent of TGF-beta; and insulin signaling to control cell growth and size; TFG-1 directly interacts with SEC-16 and controls COPII subunit accumulation at the endoplasmic reticulum exit sites; TFG-1 requires SEC-16 for its localization and SEC-16 requires TFG-1 to accumulate normally on endoplasmic reticulum exit sites; TFG-1 hexamers facilitates normal assembly of large complexes containing SEC-16 and COPII subunits; TFG-1 depletion leads to a defect in normal Golgi assembly; analogously to C. elegans TFG-1, human TFG functions at endoplasmic reticulum exit sites; TFG-1 is detectable as early as the two cell stage of embryogenesis and expression continues throughout embryogenesis, punctated pattern in cytoplasm colocalizing with mitochondrial COX1.Paper_evidenceWBPaper00032029
WBPaper00038310
Curator_confirmedWBPerson12884
Date_last_updated20 Jul 2011 00:00:00
Automated_descriptionPredicted to enable identical protein binding activity. Involved in several processes, including cellular localization; regulation of cell growth; and regulation of cell size. Located in endoplasmic reticulum exit site and mitochondrion. Expressed in germ line; hypodermis; intestine; and muscle cell. Human ortholog(s) of this gene implicated in hereditary spastic paraplegia 57. Is an ortholog of human TFG (trafficking from ER to golgi regulator).Paper_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_modelDOID:0110809Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11758)
Molecular_infoCorresponding_CDSY63D3A.5
Corresponding_transcriptY63D3A.5.1
Y63D3A.5.2
Other_sequence (37)
Associated_featureWBsf643832
WBsf657064
WBsf981137
WBsf986048
WBsf986049
WBsf986050
WBsf1011187
WBsf218772
Experimental_infoRNAi_result (41)
Expr_patternExpr8207
Expr9302
Expr1010574
Expr1032703
Expr1161314
Expr2017377
Expr2035514
AntibodyWBAntibody00001440
WBAntibody00002222
Microarray_resultsSMD_Y63D3A.5
187998_s_at
A_12_P111392
Aff_Y63D3A.5
GPL13394_WBGene00006565
GPL13914_Y63D3A.5
GPL14144_Y63D3A.5_1066-1125_0.648_48_C
GPL14144_Y63D3A.5_739-798_0.710_23_B
GPL14144_Y63D3A.5_900-959_0.814_10_A
GPL19516_CGZ0051579
GPL19516_CGZ0051580
GPL21109_Y63D3A.5.1
GPL3518_CE20336
GPL8304_CE_WBGene00006565_A
GPL8304_CE_WBGene00006565_B
GPL8673_Y63D3A_5P00038
GPL8673_Y63D3A_5P00513
GPL8673_Y63D3A_5P01397
GPL9450_Y63D3A.5
cea2.p.23069
Expression_cluster (128)
Interaction (306)
Map_infoMapIPosition23.1465Error0.009709
PositivePositive_cloneY63D3AInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00024063
WBPaper00031805
WBPaper00032029
WBPaper00038310
WBPaper00038491
WBPaper00055090
WBPaper00062388
RemarkSequence connection from [Mencinger M, Aman P]
Map position created from combination of previous interpolated map position (based on known location of sequence) and allele information. Therefore this is not a genetic map position based on recombination frequencies or genetic experiments. This was done on advice of the CGC.CGC_data_submission
MethodGene