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WormBase Tree Display for Gene: WBGene00020693

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Name Class

WBGene00020693SMapS_parentSequenceCHROMOSOME_I
IdentityVersion2
NameCGC_namelron-8Person_evidenceWBPerson637
Sequence_nameT22E7.1
Molecular_nameT22E7.1a
T22E7.1a.1
CE31368
T22E7.1b
CE33189
T22E7.1b.1
Other_nameCELE_T22E7.1Accession_evidenceNDBBX284601
Public_namelron-8
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:03WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
209 Dec 2011 15:47:23WBPerson2970Name_changeCGC_namelron-8
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classlron
Allele (49)
StrainWBStrain00047619
RNASeq_FPKM (74)
GO_annotation00083597
00083598
00095371
Ortholog (49)
ParalogWBGene00004854Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00007261Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013542Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00022129Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to be located in extracellular matrix and extracellular space. Expressed in body wall musculature; head muscle; pharynx; and rectal gland cell. Human ortholog(s) of this gene implicated in several diseases, including autosomal recessive intellectual developmental disorder 64; congenital stationary night blindness 1A; and stomach cancer. Is an ortholog of several human genes including LRRN1 (leucine rich repeat neuronal 1); LRRN2 (leucine rich repeat neuronal 2); and LRRN3 (leucine rich repeat neuronal 3).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:0110870Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8082)
DOID:1686Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:21205)
DOID:0081225Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:21205)
DOID:10534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20980)
DOID:8499Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:8082)
Molecular_infoCorresponding_CDST22E7.1a
T22E7.1b
Corresponding_transcriptT22E7.1a.1
T22E7.1b.1
Other_sequenceFD517495.1
CSC02279_1
Associated_featureWBsf643311
WBsf983767
WBsf217708
Experimental_infoRNAi_resultWBRNAi00028132Inferred_automaticallyRNAi_primary
WBRNAi00002855Inferred_automaticallyRNAi_primary
WBRNAi00053838Inferred_automaticallyRNAi_primary
WBRNAi00019030Inferred_automaticallyRNAi_primary
WBRNAi00053839Inferred_automaticallyRNAi_primary
Expr_patternExpr9904
Expr1025304
Expr1039013
Expr1157389
Expr2013281
Expr2031512
Drives_constructWBCnstr00014390
WBCnstr00024955
Construct_productWBCnstr00014390
WBCnstr00024955
Microarray_results (27)
Expression_cluster (149)
InteractionWBInteraction000566467
WBInteraction000566746
Map_infoMapIPosition0.445629
PositivePositive_cloneT22E7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
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