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WormBase Tree Display for Gene: WBGene00003905

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Name Class

WBGene00003905SMapS_parentSequenceY18D10A
IdentityVersion1
NameCGC_namepad-1Person_evidenceWBPerson437
Sequence_nameY18D10A.13
Molecular_nameY18D10A.13
Y18D10A.13.1
CE27468
Other_nameY18D10A15Paper_evidenceWBPaper00012822
CELE_Y18D10A.13Accession_evidenceNDBBX284601
Public_namepad-1
DB_infoDatabaseAceViewgene1N493
WormQTLgeneWBGene00003905
WormFluxgeneWBGene00003905
NDBlocus_tagCELE_Y18D10A.13
PanthergeneCAEEL|WormBase=WBGene00003905|UniProtKB=Q9XW10
familyPTHR14042
NCBIgene173156
RefSeqproteinNM_060851.7
SwissProtUniProtAccQ9XW10
TREEFAMTREEFAM_IDTF316855
UniProt_GCRPUniProtAccQ9XW10
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classpad
Allele (476)
Possibly_affected_byWBVar02157842
WBVar02157843
WBVar02157844
StrainWBStrain00001513
WBStrain00001514
WBStrain00051418
RNASeq_FPKM (74)
GO_annotation00102967
00102968
00102969
00102970
00111976
Ortholog (49)
Structured_descriptionConcise_descriptionThe pad-1 gene encodes a highly conserved, but unfamiliar, protein that is required for embryonic development.Paper_evidenceWBPaper00004319
WBPaper00012822
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to be involved in Golgi to endosome transport and protein transport. Predicted to be located in endosome and trans-Golgi network. Expressed in head and tail. Used to study Down syndrome. Is an ortholog of human DOP1A (DOP1 leucine zipper like protein A) and DOP1B (DOP1 leucine zipper like protein B).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_infoExperimental_modelDOID:14250Homo sapiensPaper_evidenceWBPaper00004319
Curator_confirmedWBPerson324
Date_last_updated29 May 2017 00:00:00
Disease_relevanceHuman Dopey family member 2(C21ORF5/DOPEY2), is located within the Down syndrome critical region of chromosome 21, which is associated with Down Syndrome; mutations in the elegans ortholog of DOPEY2, pad-1, cause embryonic lethality with most of the embryo failing to undergo proper patterning.Homo sapiensPaper_evidenceWBPaper00004319
Curator_confirmedWBPerson324
Date_last_updated29 May 2017 00:00:00
Models_disease_in_annotationWBDOannot00000166
Molecular_infoCorresponding_CDSY18D10A.13
Corresponding_CDS_historyY18D10A.13:wp49
Corresponding_transcriptY18D10A.13.1
Other_sequence (43)
Associated_feature (19)
Experimental_infoRNAi_result (17)
Expr_patternChronogram873
Expr6900
Expr6901
Expr13702
Expr1025004
Expr1031842
Expr1159115
Expr2014679
Expr2032912
Drives_constructWBCnstr00002370
WBCnstr00002371
Microarray_results (23)
Expression_cluster (90)
InteractionWBInteraction000042764
WBInteraction000046338
WBInteraction000568010
WBInteraction000583067
Map_infoMapIPosition14.1738Error0.003186
PositivePositive_cloneY18D10AInferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (17)
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