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WormBase Tree Display for Gene: WBGene00009829

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Name Class

WBGene00009829SMapS_parentSequenceF47G9
IdentityVersion2
NameCGC_nametmed-10Person_evidenceWBPerson451
Sequence_nameF47G9.1
Molecular_nameF47G9.1
F47G9.1.1
CE05883
Other_nameCELE_F47G9.1Accession_evidenceNDBBX284605
Public_nametmed-10
DB_infoDatabaseAceViewgene5L804
WormQTLgeneWBGene00009829
WormFluxgeneWBGene00009829
NDBlocus_tagCELE_F47G9.1
PanthergeneCAEEL|WormBase=WBGene00009829|UniProtKB=Q20546
familyPTHR22811
NCBIgene179567
RefSeqproteinNM_073478.6
TREEFAMTREEFAM_IDTF313729
TrEMBLUniProtAccQ20546
UniProt_GCRPUniProtAccQ20546
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
209 Jan 2019 16:22:24WBPerson1983Name_changeCGC_nametmed-10
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classtmed
Allele (46)
StrainWBStrain00003538
RNASeq_FPKM (74)
GO_annotation00068371
00068372
00068373
00068374
00068375
00068376
00068377
00068378
00068379
Contained_in_operonCEOP5522
Ortholog (38)
ParalogWBGene00004766Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00007743Caenorhabditis elegansFrom_analysisPanther
WBGene00011606Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00013360Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00019003Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00022255Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010670Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to be involved in Golgi organization; endoplasmic reticulum to Golgi vesicle-mediated transport; and intracellular protein transport. Predicted to be located in intracellular membrane-bounded organelle. Human ortholog(s) of this gene implicated in Alzheimer's disease. Is an ortholog of human TMED10 (transmembrane p24 trafficking protein 10).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:10652Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16998)
Molecular_infoCorresponding_CDSF47G9.1
Corresponding_transcriptF47G9.1.1
Other_sequence (75)
Associated_featureWBsf653098
WBsf234525
Experimental_infoRNAi_resultWBRNAi00092558Inferred_automaticallyRNAi_primary
WBRNAi00047692Inferred_automaticallyRNAi_primary
WBRNAi00092563Inferred_automaticallyRNAi_primary
WBRNAi00092565Inferred_automaticallyRNAi_primary
WBRNAi00032457Inferred_automaticallyRNAi_primary
WBRNAi00092560Inferred_automaticallyRNAi_primary
WBRNAi00080634Inferred_automaticallyRNAi_primary
Expr_patternChronogram484
Expr6108
Expr1019157
Expr1034295
Expr1151531
Expr2003867
Expr2022090
Drives_constructWBCnstr00003992
WBCnstr00031887
Construct_productWBCnstr00031887
Microarray_results (21)
Expression_cluster (119)
Interaction (67)
Map_infoMapVPosition3.07447
PositivePositive_cloneF47G9Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00024200
WBPaper00038491
WBPaper00055090
RemarkMap 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