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WormBase Tree Display for Gene: WBGene00002247

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Name Class

WBGene00002247SMapS_parentSequenceW03F8
IdentityVersion2
NameCGC_namelam-1Person_evidenceWBPerson1052
Sequence_nameW03F8.5
Molecular_nameW03F8.5a
W03F8.5a.1
CE47338
W03F8.5b
CE49160
W03F8.5b.1
Other_nameLAMB/1
CELE_W03F8.5Accession_evidenceNDBBX284604
Public_namelam-1
DB_infoDatabaseAceViewgene4F943
WormQTLgeneWBGene00002247
WormFluxgeneWBGene00002247
NDBlocus_tagCELE_W03F8.5
PanthergeneCAEEL|WormBase=WBGene00002247|UniProtKB=O44565
familyPTHR10574
NCBIgene177292
RefSeqproteinNM_068333.6
NM_001380214.1
TrEMBLUniProtAccV6CIX7
O44565
UniProt_GCRPUniProtAccO44565
OMIMgene150240
150310
150325
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:27WBPerson1971EventImportedInitial conversion from geneace
230 Jan 2012 16:23:16WBPerson1867EventAcquires_mergeWBGene00020998
Acquires_mergeWBGene00020998
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlam
Allele (90)
Legacy_information[C.elegansII] rh219 : resembles Epi-1, basal lamina missing or defective in epidermis, gonad, intestine;abnormal excretory canals, muscle cell positions, sheath cells, proximal gonad, basement membranes, ray morphology. rh219/Df is larval lethal. Cloned: rescued by cosmid C24D10, encodes lamininbeta chain. [NJ]
StrainWBStrain00037319
WBStrain00037470
RNASeq_FPKM (74)
GO_annotation00032878
00032879
00032880
00032881
00032882
00032883
00032884
00032885
00032886
Contained_in_operonCEOP4156
Ortholog (53)
ParalogWBGene00001328Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006787Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00002248Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00018304Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006432Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006746Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00016913Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020581Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptionlam-1 encodes a laminin beta that affects degenerin-induced cell death and is required redundantly with lam-2 for morphogenesis.Paper_evidenceWBPaper00015206
WBPaper00023289
Curator_confirmedWBPerson48
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionInvolved in pharynx development and positive regulation of locomotion. Located in basement membrane. Expressed in intestine. Human ortholog(s) of this gene implicated in several diseases, including Pierson syndrome; amelogenesis imperfecta type 1A; and lung carcinoma (multiple). Is an ortholog of human LAMB1 (laminin subunit beta 1) and LAMB2 (laminin subunit beta 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_modelDOID:5409Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6490)
DOID:3908Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6490)
DOID:0080380Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6487)
DOID:1070Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6487)
DOID:12849Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6486)
DOID:3209Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6490)
DOID:0110054Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6490)
DOID:0112230Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6486)
DOID:0060852Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6487)
Molecular_infoCorresponding_CDSW03F8.5a
W03F8.5b
Corresponding_CDS_historyW03F8.5:wp101
W03F8.5:wp230
Corresponding_transcriptW03F8.5a.1
W03F8.5b.1
Other_sequence (45)
Associated_feature (11)
Experimental_infoRNAi_result (20)
Expr_patternExpr3984
Expr10827
Expr1019727
Expr1031321
Expr1158236
Expr1158240
Expr2013007
Expr2031239
Drives_constructWBCnstr00005458
WBCnstr00005751
WBCnstr00006684
WBCnstr00008702
WBCnstr00008703
WBCnstr00008704
WBCnstr00008752
WBCnstr00022483
WBCnstr00024738
Construct_productWBCnstr00005458
WBCnstr00005751
WBCnstr00008752
WBCnstr00017755
WBCnstr00022483
WBCnstr00022851
WBCnstr00024738
Microarray_results (37)
Expression_cluster (203)
Interaction (39)
Anatomy_functionWBbtf0735
WBbtf0736
Map_infoMapIVPosition1.55302Error0.001128
PositivePositive_clone (3)
Mapping_dataMulti_point4471
5450
Pseudo_map_position
Reference (28)
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