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WormBase Tree Display for Gene: WBGene00004876

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Name Class

WBGene00004876EvidenceCGC_data_submission
SMapS_parentSequenceK11G12
IdentityVersion1
NameCGC_namesmf-1Person_evidenceWBPerson168
Sequence_nameK11G12.4
Molecular_nameK11G12.4a
K11G12.4a.1
CE41828
K11G12.4b
Other_nameCELE_K11G12.4Accession_evidenceNDBBX284606
Public_namesmf-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:36WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classsmf
Allele (54)
StrainWBStrain00032188
WBStrain00021956
RNASeq_FPKM (74)
GO_annotation (27)
Contained_in_operonCEOPX080
Ortholog (33)
ParalogWBGene00004877Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
Panther
WormBase-Compara
WBGene00004878Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionsmf-1 encodes one of three C. elegans divalent-metal ion transporters (DMTs) orthologous to the mammalian DMT1 transporters and Saccharomyces cerevisiae Smf proteins; in C. elegans, SMF-1 plays a minor role in manganese uptake, although mutations in smf-1 do display an increased tolerance to manganese exposure; SMF-1 is broadly expressed fromlate embryogenesis through adulthood, with strongest expression seen in the intestine and its associated gland cells; in epithelia, SMF-1 displays partially overlapping localization at the apical plasma membrane with SMF-3; smf-1 transcription is regulated in response to manganese; when expressed in Saccharomyces cerevisiae, smf-1 can rescue the EGTA hypersensitivity of Smf1+2 mutants.Paper_evidenceWBPaper00035485
Curator_confirmedWBPerson1843
Date_last_updated04 Aug 2010 00:00:00
Automated_descriptionPredicted to enable cadmium ion transmembrane transporter activity; iron ion transmembrane transporter activity; and manganese ion transmembrane transporter activity. Involved in monoatomic cation homeostasis; negative regulation of cellular response to manganese ion; and response to manganese ion. Located in apical plasma membrane. Expressed in several structures, including excretory cell; hermaphrodite gonad; intestine; nerve ring; and neurons. Human ortholog(s) of this gene implicated in several diseases, including autoimmune disease (multiple); leishmaniasis (multiple); and neurodegenerative disease (multiple). Is an ortholog of human SLC11A1 (solute carrier family 11 member 1) and SLC11A2 (solute carrier family 11 member 2).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_model (25)
Molecular_infoCorresponding_CDSK11G12.4a
Corresponding_CDS_historyK11G12.4:wp129
K11G12.4a:wp184
K11G12.4b:wp248
Corresponding_transcriptK11G12.4b
K11G12.4a.1
Other_sequence (32)
Associated_featureWBsf237512
Experimental_infoRNAi_resultWBRNAi00017020Inferred_automaticallyRNAi_primary
WBRNAi00050614Inferred_automaticallyRNAi_primary
WBRNAi00108000Inferred_automaticallyRNAi_primary
WBRNAi00082085Inferred_automaticallyRNAi_primary
WBRNAi00108005Inferred_automaticallyRNAi_primary
WBRNAi00050613Inferred_automaticallyRNAi_primary
WBRNAi00082079Inferred_automaticallyRNAi_primary
WBRNAi00076571Inferred_automaticallyRNAi_primary
WBRNAi00082080Inferred_automaticallyRNAi_primary
WBRNAi00082083Inferred_automaticallyRNAi_primary
Expr_patternExpr8811
Expr8859
Expr12160
Expr1015427
Expr1032417
Expr1154320
Expr2015904
Expr2034137
Drives_constructWBCnstr00013568
WBCnstr00019898
WBCnstr00020298
WBCnstr00035346
Construct_productWBCnstr00013568
WBCnstr00013569
WBCnstr00019900
WBCnstr00035346
AntibodyWBAntibody00001996
Microarray_results (22)
Expression_cluster (93)
InteractionWBInteraction000120474
WBInteraction000122885
WBInteraction000162127
WBInteraction000175425
WBInteraction000176008
WBInteraction000194893
WBInteraction000204494
WBInteraction000207243
WBInteraction000209000
WBInteraction000213593
WBInteraction000234669
WBInteraction000236821
WBInteraction000257591
WBInteraction000270899
WBInteraction000295074
WBInteraction000303537
WBInteraction000309325
WBInteraction000316006
WBInteraction000322431
WBInteraction000337515
WBInteraction000362954
WBInteraction000407672
WBInteraction000425447
WBInteraction000425448
WBInteraction000428002
WBInteraction000448101
WBInteraction000464078
WBInteraction000465881
WBInteraction000466604
WBInteraction000467365
WBInteraction000468148
WBInteraction000469043
WBInteraction000470931
WBInteraction000471208
WBInteraction000504045
WBProcessWBbiopr:00000096
Map_infoMapXPosition-2.5294Error0.00832
PositivePositive_cloneK11G12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4665
4666
Pseudo_map_position
Reference (18)
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