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WormBase Tree Display for Gene: WBGene00002179

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Name Class

WBGene00002179EvidencePaper_evidenceWBPaper00005001
SMapS_parentSequenceT22C1
IdentityVersion1
NameCGC_namejph-1Person_evidenceWBPerson459
Sequence_nameT22C1.7
Molecular_nameT22C1.7
T22C1.7.1
CE30566
Other_nameJP
CELE_T22C1.7Accession_evidenceNDBBX284601
Public_namejph-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:26WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classjph
Allele (72)
StrainWBStrain00037229
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (51)
Structured_descriptionConcise_descriptionjph-1 encodes a junctophilin, a protein that belongs to a transmembrane family of proteins implicated in the formation of the junctional membrane complex that forms between the plasma membrane and the endoplasmic reticulum in excitable cells; this complex facilitates cross-talk between the cell surface and intracellular ionic channels; RNA interference of jph-1 results in a locomotion defect suggesting impaired body-wall muscle function; a jph-1 promoter-gfp fusion reporter is expressed in all muscle cells and certain neurons of the nerve ring.Paper_evidenceWBPaper00005001
Curator_confirmedWBPerson324
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable structural molecule activity. Involved in locomotion and positive regulation of engulfment of apoptotic cell. Predicted to be located in endoplasmic reticulum membrane and plasma membrane. Predicted to be part of junctional membrane complex. Expressed in body wall musculature; muscle cell; and nerve ring. Human ortholog(s) of this gene implicated in Charcot-Marie-Tooth disease axonal type 2K; Huntington's disease-like 2; and intrinsic cardiomyopathy (multiple). Is an ortholog of human JPH3 (junctophilin 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:0110323Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14202)
DOID:0090104Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14203)
DOID:0081161Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14202)
DOID:0110167Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14201)
Molecular_infoCorresponding_CDST22C1.7
Corresponding_CDS_historyT22C1.7:wp77
Corresponding_transcriptT22C1.7.1
Other_sequence (22)
Associated_feature (14)
Experimental_infoRNAi_resultWBRNAi00053811Inferred_automaticallyRNAi_primary
WBRNAi00116592Inferred_automaticallyRNAi_primary
WBRNAi00097815Inferred_automaticallyRNAi_primary
WBRNAi00026354Inferred_automaticallyRNAi_primary
WBRNAi00065168Inferred_automaticallyRNAi_primary
WBRNAi00026355Inferred_automaticallyRNAi_primary
WBRNAi00004263Inferred_automaticallyRNAi_primary
Expr_patternExpr1724
Expr1935
Expr3200
Expr15971
Expr15972
Expr1019027
Expr1031274
Expr1157358
Expr2012895
Expr2031129
Drives_constructWBCnstr00010417
WBCnstr00010527
WBCnstr00011213
WBCnstr00036406
WBCnstr00042623
Construct_productWBCnstr00036406
WBCnstr00042623
Microarray_results (25)
Expression_cluster (161)
Interaction (51)
Map_infoMapIPosition2.41451Error0.001218
PositivePositive_cloneT22C1Inferred_automaticallyFrom CDS info
From sequence, transcript, pseudogene data
Pseudo_map_position
Reference (13)
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