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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
Reference (16)
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