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WormBase Tree Display for Gene: WBGene00001815

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Name Class

WBGene00001815SMapS_parentSequenceW09D6
IdentityVersion2
NameCGC_namehmt-1Person_evidenceWBPerson583
WBPerson36
WBPerson4191
Sequence_nameW09D6.6
Molecular_nameW09D6.6
W09D6.6.1
CE31731
Other_namehaf-5Person_evidenceWBPerson583
WBPerson36
WBPerson4191
CELE_W09D6.6Accession_evidenceNDBBX284603
Public_namehmt-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:25WBPerson1971EventImportedInitial conversion from geneace
210 Dec 2004 17:13:40WBPerson2970Name_changeCGC_namehmt-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhmt
Allele (127)
StrainWBStrain00001122
WBStrain00001123
WBStrain00035619
WBStrain00035648
WBStrain00039998
WBStrain00039999
WBStrain00040000
WBStrain00040001
RNASeq_FPKM (74)
GO_annotation (33)
Contained_in_operonCEOP3884
Ortholog (40)
Paralog (23)
Structured_descriptionConcise_descriptionhmt-1 encodes a predicted transmembrane half-molecule ATP-binding cassette (ABC) transporter orthologous to Schizosaccharomyces pombe heavy metal tolerance factor 1 (SpHMT1), an ATP-dependent phytochelatin transporter; HMT-1 is required for cadmium detoxification and by homology, is predicted to promote sequestration of heavy metal-containing phytochelatins into intracellular vacuoles to protect cells from potential damage.Paper_evidenceWBPaper00004424
WBPaper00025092
Curator_confirmedWBPerson1843
Date_last_updated16 Jul 2007 00:00:00
Automated_descriptionEnables cadmium ion transmembrane transporter activity. Involved in cadmium ion transmembrane transport; cellular detoxification of cadmium ion; and detoxification of copper ion. Located in endosome and vacuolar membrane. Expressed in coelomocyte; head neurons; intestinal cell; and tail neurons. Human ortholog(s) of this gene implicated in dyschromatosis universalis hereditaria. Is an ortholog of human ABCB6 (ATP binding cassette subfamily B member 6 (Langereis blood group)).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:0060304Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:47)
EFO:MONDO:0000170Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:47)
Molecular_infoCorresponding_CDSW09D6.6
Corresponding_CDS_historyW09D6.6:wp59
W09D6.6:wp84
Corresponding_transcriptW09D6.6.1
Other_sequence (46)
Associated_featureWBsf994264
WBsf994265
WBsf994266
WBsf994267
WBsf994268
WBsf1015925
WBsf227543
Experimental_infoRNAi_resultWBRNAi00078484Inferred_automaticallyRNAi_primary
WBRNAi00006067Inferred_automaticallyRNAi_primary
WBRNAi00036408Inferred_automaticallyRNAi_primary
WBRNAi00078227Inferred_automaticallyRNAi_primary
WBRNAi00078228Inferred_automaticallyRNAi_primary
WBRNAi00055049Inferred_automaticallyRNAi_primary
WBRNAi00061908Inferred_automaticallyRNAi_primary
Expr_pattern (13)
Drives_constructWBCnstr00002005
WBCnstr00002030
WBCnstr00006912
WBCnstr00007020
WBCnstr00011352
WBCnstr00013806
Construct_productWBCnstr00013806
WBCnstr00016459
Microarray_results (22)
Expression_cluster (122)
Interaction (12)
WBProcessWBbiopr:00000065
WBbiopr:00000096
Map_infoMapIIIPosition5.95263Error0.021609
PositivePositive_cloneW09D6Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4392
4943
Pseudo_map_position
ReferenceWBPaper00010259
WBPaper00025092
WBPaper00027644
WBPaper00028961
WBPaper00028970
WBPaper00031484
WBPaper00033962
WBPaper00036020
WBPaper00037566
WBPaper00037584
WBPaper00037585
WBPaper00037664
WBPaper00038491
WBPaper00050414
WBPaper00055090
WBPaper00056729
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