Questions, Feedback & Help
Send us an email and we'll get back to you ASAP. Or you can read our Frequently Asked Questions.

WormBase Tree Display for Gene: WBGene00001650

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00001650SMapS_parentSequenceCHROMOSOME_IV
IdentityVersion1
NameCGC_namegon-1Person_evidenceWBPerson261
Sequence_nameF25H8.3
Molecular_nameF25H8.3a
F25H8.3a.1
CE42668
F25H8.3b
CE46622
F25H8.3a.2
F25H8.3b.1
F25H8.3c
Other_nameCELE_F25H8.3Accession_evidenceNDBBX284604
Public_namegon-1
DB_infoDatabase (14)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:25WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgon
Allele (221)
Legacy_information[C.elegansII] e1254 : defective formation of somatic gonad primordium; much germ line proliferation, almost no gamete maturation, variable vulval induction, no uterus. e1254/Df similar.ES3. ME0 (male somatic gonad also abnormal). OA4:e2547, e2551, q517, q518 (similar). [Hodgkin et al. 1989; CB; JK]
StrainWBStrain00022578
WBStrain00022613
WBStrain00004564
WBStrain00050795
WBStrain00054932
WBStrain00054931
RNASeq_FPKM (74)
GO_annotation (30)
Ortholog (56)
ParalogWBGene00000082Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00000083Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00086562Caenorhabditis elegansFrom_analysisPanther
WBGene00003242Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00009958Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020567Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00021171Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00003248Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptiongon-1 encodes a functional metalloprotease that defines a new sub-family of secreted proteases known as MPT (metalloprotease with thrombospondin type 1 repeats); the other two members of this family are the bovine procollagen I N-protease ( PINP ) and the murine enzyme ADAMTS-1; gon-1 is essential for hermaphrodite gonadal morphogenesis and sequence homology with other metalloproteases suggests that it functions by remodeling the extracellular matrix; gon-1 is also required for protein transport from the endoplasmic reticulum (ER) to the Golgi, a function dependent on its C-terminal GON domain; GON-1 is expressed at high levels within the gonadal distal tip cell during migration and also in body wall muscle cells; in the distal tip cell, reporter fusion constructs expressing the GON domain localize to the endoplasmic reticulum, suggesting that GON-1 functions both intra- and extracellularly.Paper_evidenceWBPaper00003556
WBPaper00003841
WBPaper00040883
Curator_confirmedWBPerson1843
WBPerson324
Date_last_updated16 Mar 2012 00:00:00
Automated_descriptionEnables metallopeptidase activity. Involved in several processes, including endoplasmic reticulum to Golgi vesicle-mediated transport; muscle organ morphogenesis; and negative regulation of presynapse assembly. Predicted to be located in extracellular matrix. Expressed in amphid neurons; excretory cell; gonad; motor neurons; and muscle cell. Used to study obesity and type 2 diabetes mellitus. Human ortholog(s) of this gene implicated in rheumatoid arthritis. Is an ortholog of human ADAMTS20 (ADAM metallopeptidase with thrombospondin type 1 motif 20) and ADAMTS9 (ADAM metallopeptidase with thrombospondin type 1 motif 9).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_infoExperimental_modelDOID:9352Homo sapiensPaper_evidenceWBPaper00048391
Curator_confirmedWBPerson324
Date_last_updated28 Oct 2015 00:00:00
DOID:9970Homo sapiensPaper_evidenceWBPaper00061889
Curator_confirmedWBPerson324
Date_last_updated28 Jun 2022 00:00:00
Potential_modelDOID:7148Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:220)
Models_disease_in_annotationWBDOannot00000381
WBDOannot00001255
Molecular_infoCorresponding_CDSF25H8.3a
F25H8.3b
Corresponding_CDS_historyF25H8.3:wp191
Corresponding_transcriptF25H8.3c
F25H8.3a.1
F25H8.3a.2
F25H8.3b.1
Other_sequenceJI164015.1
Dviv_isotig32909
MP00069
CBC09661_1
Dviv_isotig16135
Oden_isotig19638
Hbac_isotig07485
Associated_feature (17)
Experimental_infoRNAi_result (23)
Expr_pattern (11)
Drives_constructWBCnstr00003119
WBCnstr00010223
WBCnstr00021147
WBCnstr00021148
WBCnstr00036796
Construct_productWBCnstr00016199
WBCnstr00020015
WBCnstr00036796
Microarray_results (23)
Expression_cluster (151)
Interaction (36)
Map_infoMapIVPosition4.4533Error0.0006
Well_ordered
PositivePositive_cloneF25H8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point1611
3732
3733
3734
Pos_neg_data4643
4644
Reference (59)
MethodGene