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WormBase Tree Display for Gene: WBGene00009306

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Name Class

WBGene00009306SMapS_parentSequenceF32A7
IdentityVersion2
NameCGC_namemaph-1.1Person_evidenceWBPerson805
Sequence_nameF32A7.5
Molecular_name (12)
Other_nameCELE_F32A7.5Accession_evidenceNDBBX284601
Public_namemaph-1.1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:50WBPerson1971EventImportedInitial conversion from CDS class of WS125
203 Jul 2015 12:05:46WBPerson2970Name_changeCGC_namemaph-1.1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmaph
AlleleWBVar02147173
WBVar02156489
WBVar00298088
WBVar00298089
WBVar01915645
WBVar01499908
WBVar00543302
WBVar00543303
WBVar01499739
WBVar00694343
WBVar00694344
WBVar00694345
WBVar00694346
WBVar00694347
WBVar00694348
WBVar00694349
WBVar00694350
WBVar00694351
WBVar00694352
WBVar00694353
WBVar00598092
WBVar00162604
WBVar00694354
WBVar00694355
WBVar00694356
WBVar00694357
WBVar00694358
WBVar00694359
WBVar00694360
WBVar00694361
WBVar00694362
WBVar00694363
WBVar00694364
WBVar00694365
WBVar00694366
WBVar00694367
WBVar00694368
WBVar00694369
WBVar00694370
WBVar00694371
WBVar00694372
WBVar00694373
WBVar00694374
WBVar00694375
WBVar00694376
WBVar00694377
WBVar00694378
WBVar00694379
WBVar00694380
WBVar00694381
WBVar00694382
WBVar00694383
WBVar00694384
WBVar01499066
WBVar01502751
WBVar01502752
WBVar01502753
WBVar01499627
WBVar01499628
WBVar01499999
WBVar01499823
WBVar01499298
WBVar01498939
WBVar00353383
WBVar00353384
WBVar00353385
WBVar00353386
WBVar00353387
WBVar00353388
WBVar00353389
WBVar00353390
WBVar00353391
WBVar00353392
WBVar00353393
WBVar00353394
WBVar01496935
WBVar01496936
RNASeq_FPKM (74)
GO_annotation (23)
Ortholog (48)
ParalogWBGene00007966Caenorhabditis elegansFrom_analysisTreeFam
Inparanoid_8
WormBase-Compara
WBGene00009113Caenorhabditis elegansFrom_analysisInparanoid_8
WormBase-Compara
WBGene00018325Caenorhabditis elegansFrom_analysismodENCODE_Pseudogenes
Structured_descriptionAutomated_descriptionPredicted to enable actin binding activity and microtubule binding activity. Predicted to be involved in microtubule cytoskeleton organization; neuron projection development; and regulation of microtubule depolymerization. Located in microtubule cytoskeleton. Expressed in body wall musculature; egg-laying apparatus; hypodermis; intestinal cell; and neurons. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness and periventricular nodular heterotopia. Is an ortholog of human MAP1A (microtubule associated protein 1A); MAP1B (microtubule associated protein 1B); and MAP1S (microtubule associated protein 1S).Paper_evidenceWBPaper00065943
Curator_confirmed (2)
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:0050454Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6836)
DOID:0050564Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6836)
Molecular_infoCorresponding_CDSF32A7.5a
F32A7.5b
F32A7.5c
F32A7.5d
Corresponding_transcriptF32A7.5a.1
F32A7.5b.1
F32A7.5c.1
F32A7.5d.1
Other_sequenceCJC09850_1
CRC06312_1
CR00627
CRC10472_1
CR01632
Associated_featureWBsf657122
WBsf657123
WBsf717609
WBsf986244
WBsf1011301
WBsf218840
Experimental_infoRNAi_result (41)
Expr_patternExpr13645
Expr1025913
Expr1034067
Expr1149977
Expr2013376
Expr2031608
Drives_constructWBCnstr00032296
Construct_productWBCnstr00032296
Microarray_results (30)
Expression_cluster (175)
Interaction (116)
Map_infoMapIPosition27.956
PositivePositive_cloneF32A7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00029395
WBPaper00038491
WBPaper00049959
WBPaper00055090
WBPaper00059214
WBPaper00059548
WBPaper00060754
WBPaper00062248
WBPaper00064789
WBPaper00065165
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