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WormBase Tree Display for Gene: WBGene00003411

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Name Class

WBGene00003411SMapS_parentSequenceCHROMOSOME_X
IdentityVersion1
NameCGC_namemrp-5Person_evidenceWBPerson490
Sequence_nameF14F4.3
Molecular_nameF14F4.3
F14F4.3.1
CE23650
Other_nameCELE_F14F4.3Accession_evidenceNDBBX284606
Public_namemrp-5
DB_infoDatabaseAceViewgeneXP558
WormQTLgeneWBGene00003411
WormFluxgeneWBGene00003411
NDBlocus_tagCELE_F14F4.3
PanthergeneCAEEL|WormBase=WBGene00003411|UniProtKB=G5EE72
familyPTHR24223
NCBIgene181587
RefSeqproteinNM_078078.4
SwissProtUniProtAccG5EE72
UniProt_GCRPUniProtAccG5EE72
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:31WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmrp
AlleleWBVar01499887
WBVar01499519
WBVar01499888
WBVar01499710
WBVar01782616
WBVar01942259
WBVar00525470
WBVar00525471
WBVar00525472
WBVar00525473
WBVar00525474
WBVar00525475
WBVar00093254
WBVar00525476
WBVar00525477
WBVar00525478
WBVar00525479
WBVar00525480
WBVar00525481
WBVar00525482
WBVar00525483
WBVar00525484
WBVar01528189
WBVar00525485
WBVar01528190
WBVar00525486
WBVar01528191
WBVar00525487
WBVar00525488
WBVar00525489
WBVar01897966
WBVar00525490
WBVar01760497
WBVar01760498
WBVar01760499
WBVar01472725
WBVar01472728
WBVar00265233
WBVar01928687
WBVar00255480
WBVar01928688
WBVar01788245
WBVar02035062
WBVar02027725
WBVar01211597
WBVar01211598
WBVar01211599
WBVar01211600
WBVar01211601
WBVar01211602
WBVar01211603
WBVar01211604
WBVar01211605
WBVar01211606
WBVar01211607
WBVar01211608
WBVar01211609
WBVar01211610
WBVar01211611
WBVar00085825
WBVar01211612
WBVar00085826
WBVar01211613
WBVar00085827
WBVar00313745
WBVar00085828
WBVar01211614
WBVar00313746
WBVar00085829
WBVar01211615
WBVar01211616
WBVar00085830
WBVar00313747
WBVar00313748
WBVar01211617
WBVar00085831
WBVar01211618
WBVar00085833
WBVar01211619
WBVar00085834
WBVar01211620
WBVar01211621
WBVar01211622
WBVar01211623
WBVar01211624
WBVar01211625
WBVar01211626
WBVar01211627
WBVar01211628
WBVar01211629
WBVar01211630
WBVar01211631
WBVar01211632
WBVar01211633
WBVar01211634
WBVar01211635
WBVar01211636
WBVar01211637
WBVar01211638
WBVar00218863
WBVar00218866
WBVar01211639
WBVar00218867
WBVar01211640
WBVar00218868
WBVar01211641
WBVar01211642
WBVar01211643
WBVar01211644
WBVar01602546
WBVar01211645
WBVar01602547
WBVar01211646
WBVar01602548
WBVar01211647
WBVar01211648
WBVar01211649
WBVar01211650
WBVar01211651
WBVar01211652
WBVar01211653
WBVar01211654
WBVar01498960
WBVar01500067
Strain (2)
RNASeq_FPKM (74)
GO_annotation (16)
Ortholog (41)
ParalogWBGene00000477Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003407Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003408Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003409Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003410Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003412Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003414Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003413Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionThe mrp-5 gene encodes a homolog of the human gene CFTR, which when mutated leads to cystic fibrosis (OMIM:219700).Paper_evidenceWBPaper00004424
WBPaper00004637
Curator_confirmedWBPerson567
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables ABC-type vitamin B12 transporter activity. Involved in cobalamin transport. Predicted to be located in membrane. Expressed in several structures, including body wall musculature; hypodermis; intestine; muscle cell; and pharynx. Human ortholog(s) of this gene implicated in pancreatic cancer. Is an ortholog of human ABCC12 (ATP binding cassette subfamily C member 12) and ABCC5 (ATP binding cassette subfamily C member 5).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:1793Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:56)
Molecular_infoCorresponding_CDSF14F4.3
Corresponding_CDS_historyF14F4.3a:wp252
Corresponding_transcriptF14F4.3.1
Other_sequence (48)
Associated_feature (16)
Experimental_infoRNAi_result (15)
Expr_pattern (11)
Drives_constructWBCnstr00003311
WBCnstr00011353
WBCnstr00013720
WBCnstr00019478
WBCnstr00019480
WBCnstr00036131
Construct_productWBCnstr00019479
WBCnstr00019480
WBCnstr00036131
Microarray_results (23)
Expression_cluster (188)
Interaction (42)
Map_infoMapXPosition21.5778Error0.006227
PositivePositive_cloneF14F4Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (20)
RemarkSequence connection from [Sheps JA, Baillie DL] [040902 ck1]
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