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WormBase Tree Display for Gene: WBGene00002035

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Name Class

WBGene00002035SMapS_parentSequenceF29D10
IdentityVersion1
NameCGC_namehum-1
Sequence_nameF29D10.4
Molecular_nameF29D10.4
F29D10.4.1
CE05763
Other_nameCELE_F29D10.4Accession_evidenceNDBBX284601
Public_namehum-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhum
Allele (45)
Legacy_information[C.elegansII] NMK. Encodes predicted unconventional myosin heavy chain, class I. [DU]
StrainWBStrain00003321
WBStrain00031531
WBStrain00031252
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (38)
Paralog (21)
Structured_descriptionConcise_descriptionhum-1 encodes a class I unconventional myosin heavy chain that, within this class, is most closely related to the amoeboid myosin I subclass; loss of hum-1 activity via RNAi results in a low frequency of aldicarb resistance, suggesting that hum-1 may play a role in regulating synapse structure and/or function; when expressed in the DA cholinergic motor neurons, a HUM-1 reporter fusion protein localizes solely to punctate structures.Paper_evidenceWBPaper00002905
WBPaper00026667
Curator_confirmedWBPerson1843
Date_last_updated15 Jun 2007 00:00:00
Automated_descriptionPredicted to enable actin filament binding activity and microfilament motor activity. Predicted to be involved in actin filament organization and vesicle transport along actin filament. Predicted to be located in several cellular components, including actin cytoskeleton; microvillus; and vesicle. Predicted to be part of myosin complex. Human ortholog(s) of this gene implicated in focal segmental glomerulosclerosis 6. Is an ortholog of human MYO1E (myosin IE).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:0111131Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7599)
Molecular_infoCorresponding_CDSF29D10.4
Corresponding_transcriptF29D10.4.1
Other_sequence (36)
Associated_featureWBsf655293
WBsf976874
WBsf219995
WBsf219996
Experimental_infoRNAi_result (12)
Expr_patternChronogram229
Expr3572
Expr5914
Expr1015485
Expr1031190
Expr1149826
Expr2012644
Expr2030880
Drives_constructWBCnstr00003792
WBCnstr00036505
Construct_productWBCnstr00011496
WBCnstr00036505
Microarray_results (20)
Expression_cluster (127)
Interaction (83)
Map_infoMapIPosition3.22934Error0.009405
PositivePositive_cloneF29D10Inferred_automaticallyFrom sequence, transcript, pseudogene data
T08D1Author_evidenceBaker JP
Mapping_dataMulti_point4425
4671
5011
5566
Pseudo_map_position
ReferenceWBPaper00002905
WBPaper00021651
WBPaper00024200
WBPaper00025258
WBPaper00038491
WBPaper00055090
WBPaper00064208
WBPaper00064860
Remarkdata received 11/94
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