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WormBase Tree Display for Gene: WBGene00003791

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Name Class

WBGene00003791SMapS_parentSequenceF07A11
IdentityVersion2
NameCGC_namenpp-5Person_evidenceWBPerson1780
Sequence_nameF07A11.3
Molecular_nameF07A11.3
F07A11.3.1
CE03145
Other_nameNup107Paper_evidenceWBPaper00026834
CELE_F07A11.3Accession_evidenceNDBBX284602
Public_namenpp-5
DB_infoDatabaseAceViewgene2L888
WormQTLgeneWBGene00003791
WormFluxgeneWBGene00003791
NDBlocus_tagCELE_F07A11.3
PanthergeneCAEEL|WormBase=WBGene00003791|UniProtKB=Q19131
familyPTHR13003
NCBIgene174779
RefSeqproteinNM_064080.6
SwissProtUniProtAccQ19131
UniProt_GCRPUniProtAccQ19131
OMIMgene607617
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:33WBPerson1971EventImportedInitial conversion from geneace
215 Mar 2007 08:57:28WBPerson2970Name_changeOther_nameNup107
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnpp
Allele (69)
StrainWBStrain00036637
WBStrain00003837
WBStrain00003840
WBStrain00003841
RNASeq_FPKM (74)
GO_annotation00063574
00063575
00063576
00063577
00063578
00063579
00063580
00063581
00063582
00063583
00063584
00063585
00063586
00063587
00063588
00063589
00063590
00063591
00063592
00063593
00063594
00063595
00063596
00063597
00063598
00063599
00063600
00063601
00063602
00063603
00063604
00063605
00063606
00063607
00063608
00111811
00111812
Contained_in_operonCEOP2718
Ortholog (31)
Structured_descriptionAutomated_descriptionPredicted to be a structural constituent of nuclear pore. Involved in several processes, including kinetochore assembly; protein localization to kinetochore; and regulation of nucleus size. Located in nuclear membrane. Part of nuclear pore. Human ortholog(s) of this gene implicated in Galloway-Mowat syndrome; nephrotic syndrome type 11; and ovarian dysgenesis 6. Is an ortholog of human NUP107 (nucleoporin 107).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:0080694Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29914)
DOID:0080498Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29914)
DOID:0080385Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:29914)
Molecular_infoCorresponding_CDSF07A11.3
Corresponding_transcriptF07A11.3.1
Other_sequenceCBC07538_1
CR03653
CRC05182_1
CR04595
CR03960
CRC05640_1
Associated_featureWBsf650602
WBsf666172
WBsf223966
Experimental_infoRNAi_result (11)
Expr_patternExpr1027606
Expr1031777
Expr1147819
Expr2014390
Expr2032631
Drives_constructWBCnstr00035865
Construct_productWBCnstr00005566
WBCnstr00014542
WBCnstr00035865
AntibodyWBAntibody00001891
WBAntibody00002304
Microarray_results (20)
Expression_cluster (110)
Interaction (164)
Map_infoMapIIPosition3.78634Error0.003937
PositivePositive_cloneF07A11Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00006202
WBPaper00026834
WBPaper00032497
WBPaper00036964
WBPaper00040620
WBPaper00040897
WBPaper00061547
WBPaper00063941
WBPaper00064641
WBPaper00065742
RemarkSequence connection from [Askjaer P, Mattaj IW]. krb 13/11/01
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