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WormBase Tree Display for Gene: WBGene00021354

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Name Class

WBGene00021354SMapS_parentSequenceY37E3
IdentityVersion2
NameCGC_namefpn-1.1
Sequence_nameY37E3.16
Molecular_nameY37E3.16
Y37E3.16.1
CE36732
Other_nameCELE_Y37E3.16Accession_evidenceNDBBX284601
Public_namefpn-1.1
DB_infoDatabaseWormQTLgeneWBGene00021354
WormFluxgeneWBGene00021354
NDBlocus_tagCELE_Y37E3.16
PanthergeneCAEEL|WormBase=WBGene00021354|UniProtKB=Q8IA95
familyPTHR11660
NCBIgene171773
RefSeqproteinNM_001037896.4
TREEFAMTREEFAM_IDTF313463
TrEMBLUniProtAccQ8IA95
UniProt_GCRPUniProtAccQ8IA95
OMIMgene604653
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:04WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
226 Feb 2008 14:53:11WBPerson2970Name_changeCGC_namefpn-1.1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classfpn
Allele (115)
RNASeq_FPKM (74)
GO_annotation00084031
00084032
00084033
00084034
00084035
00084036
00125733
00125734
00125735
OrthologWBGene00040721Caenorhabditis briggsaeFrom_analysisOrthoMCL
OMA
Inparanoid_8
WormBase-Compara
WBGene00060576Caenorhabditis remaneiFrom_analysisOMA
TreeFam
Inparanoid_8
WormBase-Compara
WBGene00159759Caenorhabditis brenneriFrom_analysisOMA
TreeFam
Inparanoid_8
WormBase-Compara
WBGene00155540Caenorhabditis brenneriFrom_analysisOMA
TreeFam
Inparanoid_8
WormBase-Compara
WBGene00136344Caenorhabditis japonicaFrom_analysisTreeFam
Inparanoid_8
WormBase-Compara
CBOVI.g9689Caenorhabditis bovisFrom_analysisWormBase-Compara
CSP21.g457Caenorhabditis parvicaudaFrom_analysisWormBase-Compara
CSP26.g19495Caenorhabditis zanzibariFrom_analysisWormBase-Compara
CSP28.g11470Caenorhabditis panamensisFrom_analysisWormBase-Compara
CSP29.g11057Caenorhabditis beceiFrom_analysisWormBase-Compara
CSP31.g7459Caenorhabditis uteleiaFrom_analysisWormBase-Compara
CSP32.g8866Caenorhabditis sulstoniFrom_analysisWormBase-Compara
CSP38.g21137Caenorhabditis quiockensisFrom_analysisWormBase-Compara
CSP39.g18102Caenorhabditis waitukubuliFrom_analysisWormBase-Compara
CSP39.g6815Caenorhabditis waitukubuliFrom_analysisWormBase-Compara
CSP40.g18678Caenorhabditis tribulationisFrom_analysisWormBase-Compara
Cang_2012_03_13_00001.g82Caenorhabditis angariaFrom_analysisWormBase-Compara
Cni-fpn-1.1Caenorhabditis nigoniFrom_analysisWormBase-Compara
Csp5_scaffold_00185.g6553Caenorhabditis sinicaFrom_analysisWormBase-Compara
FL83_18660Caenorhabditis latensFrom_analysisWormBase-Compara
GCK72_001083Caenorhabditis remaneiFrom_analysisWormBase-Compara
OTIPU.nOt.2.0.1.g04139Oscheius tipulaeFrom_analysisWormBase-Compara
Sp34_10236000Caenorhabditis inopinataFrom_analysisWormBase-Compara
chrI_pilon.g293Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00113652Pristionchus pacificusFrom_analysisWormBase-Compara
ZFIN:ZDB-GENE-000511-8Danio rerioFrom_analysisHieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
HGNC:10909Homo sapiensFrom_analysisHieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
MGI:1315204Mus musculusFrom_analysisHieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
RGD:620180Rattus norvegicusFrom_analysisHieranoid
Inparanoid
OMA
OrthoFinder
OrthoInspector
Panther
PhylomeDB
SonicParanoid
ParalogWBGene00019977Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable iron ion transmembrane transporter activity. Predicted to be involved in iron ion transmembrane transport. Predicted to be located in membrane. Used to study Parkinson's disease. Human ortholog(s) of this gene implicated in hemochromatosis type 4. Is an ortholog of human SLC40A1 (solute carrier family 40 member 1).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:14330Homo sapiensPaper_evidenceWBPaper00046532
Curator_confirmedWBPerson324
Date_last_updated06 May 2015 00:00:00
Potential_modelDOID:0111028Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10909)
Disease_relevanceParkinson''s disease (PD) is a common neurodegenerative disorder, characterized by selective dopaminergic (DAergic) neuron loss in the brain; symptoms include rigidity, tremors and postural instability that are often preceded by emotional instability and cognitive dysfunction; several genes confer risk for autosomal recessive PD, including the parkin/PARK2 gene that encodes for the E3 ubiquitin ligase Parkin; the heavy metal manganese (Mn) is an environmental risk factor for the development of PD; studies in C. elegans have shown significantly increased Mn accumulation in pdr-1/parkin mutants compared to wild-type animals and significant downregulation in mRNA levels of the putative manganese exporter ferroportin, fpn-1.1; overexpression of fpn-1.1 in a pdr-1 mutant strain showed suppression of Mn-induced lethality, decreased levels of pro-oxidant metals like iron and copper, and improved mitochondrial and DAergic integrity and function; these studies reveal the role of Parkin in regulating metal homeostasis.Homo sapiensPaper_evidenceWBPaper00046532
Curator_confirmedWBPerson324
Date_last_updated06 May 2015 00:00:00
Models_disease_in_annotationWBDOannot00000348
Molecular_info (5)
Experimental_infoRNAi_resultWBRNAi00055933Inferred_automaticallyRNAi_primary
Expr_patternExpr1024007
Expr1039322
Expr1159451
Expr2011875
Expr2030113
Microarray_results (17)
Expression_cluster (145)
WBProcessWBbiopr:00000096
Map_infoMapIPosition-11.481Error0.162678
PositivePositive_cloneY37E3Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00040349
WBPaper00046532
WBPaper00048451
WBPaper00049884
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