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WormBase Tree Display for Gene: WBGene00001651

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Name Class

WBGene00001651SMapS_parentSequenceCHROMOSOME_I
IdentityVersion1
NameCGC_namegon-2Person_evidenceWBPerson261
Sequence_nameT01H8.5
Molecular_name (16)
Other_nameCELE_T01H8.5Accession_evidenceNDBBX284601
Public_namegon-2
DB_infoDatabaseWormQTLgeneWBGene00001651
WormFluxgeneWBGene00001651
NDBlocus_tagCELE_T01H8.5
PanthergeneCAEEL|WormBase=WBGene00001651|UniProtKB=Q93971
familyPTHR13800
NCBIgene172646
RefSeqproteinNM_001129034.3
NM_059914.8
NM_001129033.3
NM_001373178.2
NM_001136316.4
SwissProtUniProtAccQ93971
TrEMBLUniProtAccG5EE91
A5JYU8
G5EGP7
G5EGJ6
UniProt_GCRPUniProtAccQ93971
OMIMgene603576
605692
607009
608961
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:25WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgon
Allele (294)
Legacy_information[C.elegansII] q362 :partial maternal effect gonadless (Z1 and Z4 often fail to divide). OA3: q388ts (zygotic sterile at 25C, fertile 15C, upshift gives Gon progeny), dx12, dx13. Cloned : cosmid rescue (T01H8)[EJ]
[Lambie EJ] q362 is partial maternal-effect gonadless (Z1, Z4 often fail to divide). q388 is ts allele, fertile at 15C, zygotic sterile at 25C, upshift gives Gon progeny.
StrainWBStrain00036616
WBStrain00007128
WBStrain00007130
WBStrain00007119
WBStrain00007123
WBStrain00007124
WBStrain00049840
WBStrain00049841
RNASeq_FPKM (74)
GO_annotation (20)
Ortholog (58)
ParalogWBGene00001796Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00001795Caenorhabditis elegansFrom_analysisTreeFam
Panther
WormBase-Compara
WBGene00000425Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00004149Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00008731Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00020972Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021404Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00021408Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptiongon-2 encodes a predicted transmembrane cation channel homologous to the long transient receptor potential channel (LTRPC) subfamily of TRP channels including Drosophila DLTRP and mammalian melastatin and LTRPC7; GON-2 regulates the onset and continuation of post-embryonic mitotic cell divisions in the somatic gonad precursor cells perhaps by mediating an increase in intracellular calcium in response to activating signals.Paper_evidenceWBPaper00004159
WBPaper00004647
WBPaper00018419
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable monoatomic cation channel activity. Involved in defecation; gonad development; and mitotic cell cycle. Predicted to be located in plasma membrane. Expressed in gonad and intestine. Human ortholog(s) of this gene implicated in several diseases, including amyotrophic lateral sclerosis-parkinsonism/dementia complex 1; congenital stationary night blindness 1C; and intestinal hypomagnesemia 1. Is an ortholog of human TRPM3 (transient receptor potential cation channel subfamily M member 3) and TRPM7 (transient receptor potential cation channel subfamily M member 7).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:0110867Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7146)
DOID:0050534Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7146)
DOID:0111246Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17994)
DOID:0060883Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17995)
DOID:896Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17995)
DOID:83Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:17992)
Molecular_infoCorresponding_CDST01H8.5a
T01H8.5b
T01H8.5c
T01H8.5d
T01H8.5e
Corresponding_CDS_historyT01H8.5:wp74
Corresponding_transcriptT01H8.5a.1
T01H8.5b.1
T01H8.5c.1
T01H8.5d.1
T01H8.5d.2
T01H8.5e.1
Other_sequence (30)
Associated_feature (15)
Experimental_infoRNAi_resultWBRNAi00004102Inferred_automaticallyRNAi_primary
WBRNAi00026161Inferred_automaticallyRNAi_primary
WBRNAi00052180Inferred_automaticallyRNAi_primary
WBRNAi00052181Inferred_automaticallyRNAi_primary
WBRNAi00083926Inferred_automaticallyRNAi_primary
WBRNAi00083925Inferred_automaticallyRNAi_primary
WBRNAi00116718Inferred_automaticallyRNAi_primary
WBRNAi00035042Inferred_automaticallyRNAi_primary
WBRNAi00026160Inferred_automaticallyRNAi_primary
Expr_patternExpr3712
Expr6568
Expr10982
Expr1027590
Expr1030991
Expr1155811
Expr2012171
Expr2030407
Drives_constructWBCnstr00003790
WBCnstr00006319
WBCnstr00007206
WBCnstr00011621
WBCnstr00042687
Construct_productWBCnstr00006319
WBCnstr00011621
WBCnstr00042687
WBCnstr00042688
Microarray_results (29)
Expression_cluster (115)
Interaction (56)
Map_infoMapIPosition2.95114Error0.007035
Well_ordered
PositiveInside_rearrdxDf1
Positive_cloneT01H8Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point3674
3675
4381
Pos_neg_data9323
Reference (58)
Remarksequence from Pinar Kondu.0105
T01H8.3 and T01H8.4 removed. email from JAH 0109
MethodGene