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WormBase Tree Display for Gene: WBGene00000776

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Name Class

WBGene00000776EvidencePaper_evidenceWBPaper00004821
SMapS_parentSequenceT03E6
IdentityVersion1
Name (5)
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcpl
Allele (188)
StrainWBStrain00035678
RNASeq_FPKM (74)
GO_annotation00035097
00035098
00035099
00035100
00035101
00035102
00035103
00035104
00035105
00035106
00035107
00035108
00035109
00035110
00035111
00035112
00035113
00035114
00035115
00035116
00035117
00035118
00035119
00035120
00035121
00035122
00035123
00035124
00035125
00035126
00035127
00035128
00107780
00107781
Ortholog (69)
Paralog (28)
Structured_descriptionConcise_descriptioncpl-1 encodes a member of the cathepsin L-like cysteine protease family required for embryonic viability and normal growth; expressed in eggshells and throughout early embryos, accumulates in intestinal cells during late embryogenesis, and expressed in the cuticle, gonad, and pharynx later in development.Paper_evidenceWBPaper00005099
WBPaper00005654
WBPaper00011657
WBPaper00023209
Curator_confirmedWBPerson48
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable cysteine-type endopeptidase activity. Involved in several processes, including lipid droplet disassembly; positive regulation of vitellogenesis; and regulation of apoptosis involved in tissue homeostasis. Located in several cellular components, including lysosome; vesicle lumen; and yolk granule. Expressed in several structures, including cuticle; eggshell; hermaphrodite gonad; pharynx; and vulva. Human ortholog(s) of this gene implicated in hypertrophic cardiomyopathy and type 2 diabetes mellitus. Is an ortholog of human CTSL (cathepsin L).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:11984Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2537)
DOID:9352Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:2537)
Molecular_infoCorresponding_CDST03E6.7a
T03E6.7b
Corresponding_transcriptT03E6.7a.1
T03E6.7b.1
Other_sequence (287)
Associated_feature (13)
Experimental_infoRNAi_result (20)
Expr_pattern (17)
Drives_constructWBCnstr00002531
WBCnstr00010433
WBCnstr00010434
WBCnstr00019401
WBCnstr00037285
Construct_productWBCnstr00010434
WBCnstr00015512
WBCnstr00016652
WBCnstr00018463
WBCnstr00018464
WBCnstr00019401
WBCnstr00037285
Regulate_expr_clusterWBPaper00064728:cpl-1(W32AY35A)_upregulated
AntibodyWBAntibody00000451
WBAntibody00000800
WBAntibody00000801
WBAntibody00000802
WBAntibody00000803
WBAntibody00002885
WBAntibody00002910
Microarray_results (23)
Expression_cluster (236)
Interaction (107)
Map_infoMapVPosition10.72
PositivePositive_cloneT03E6Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Mapping_dataMulti_point4236
Pseudo_map_position
Reference (37)
RemarkSequence connection from [Hashmi S, Britton C, Lustigman S], 02/06/13 krb.
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
[200225 pad] Modified Map position as it was a reverse physical that could not be fixed by automated methods. (10.5333)
MethodGene