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WormBase Tree Display for Gene: WBGene00007635

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Name Class

WBGene00007635SMapS_parentSequenceCHROMOSOME_X
IdentityVersion2
NameCGC_namenpr-4Paper_evidenceWBPaper00033064
Person_evidenceWBPerson2136
Sequence_nameC16D6.2
Molecular_name (14)
Other_nameCELE_C16D6.2Accession_evidenceNDBBX284606
Public_namenpr-4
DB_infoDatabaseAceViewgeneXN154
WormQTLgeneWBGene00007635
WormFluxgeneWBGene00007635
NDBlocus_tagCELE_C16D6.2
PanthergeneCAEEL|WormBase=C16D6.2b|UniProtKB=A0A0K3AYF5
familyPTHR45695
NCBIgene182684
RefSeqproteinNM_001313375.3
NM_001307873.3
NM_077700.7
NM_001307874.4
TrEMBLUniProtAccA0A0K3AYF5
A0A078BS36
A0A078BTK0
O62062
UniProt_GCRPUniProtAccA0A0K3AYF5
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
220 Dec 2011 16:46:04WBPerson2970Name_changeCGC_namenpr-4
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnpr
Allele (213)
RNASeq_FPKM (74)
GO_annotation (17)
Ortholog (34)
Paralog (19)
Structured_descriptionAutomated_descriptionPredicted to enable G protein-coupled receptor activity. Involved in regulation of muscle contraction. Predicted to be located in membrane. Expressed in several structures, including PQR; coelomocyte; interneuron; nerve ring; and rectal gland cell. Used to study Parkinson's disease. Human ortholog(s) of this gene implicated in hypertension. Is an ortholog of human PRLHR (prolactin releasing hormone receptor).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:14330Homo sapiensPaper_evidenceWBPaper00041253
Curator_confirmedWBPerson324
Date_last_updated18 Nov 2013 00:00:00
Potential_modelDOID:10763Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4464)
Disease_relevanceIn elegans, alpha-synuclein (alpha-syn) toxicity, implicated in Parkinson''s disease and other synucleinopathies, is modeled by expressing it from the dopamine transporter (dat-1) gene promotor in transgenic GFP worms, resulting in an age-dependent progressive loss of dopaminergic neurons; using this system, it was seen that the knock-down of specific candidate genes in elegans, that interact with catp-6/ATP13A2, resulted in significant enhancement of alpha-syn-induced dopaminergic neurodegeneration; these catp-6/ATP13A2 interactors include the elegans ortholog of neuropeptide Y receptor Y1 (npr-4), AP2 associated kinase 1 (AAK1; sel-5), coagulation factor II (thrombin) receptor (dop-2 and npr-24), histone deacetylase 6 (hda-6), and YIP1 interacting factor homolog A (yif-1).Homo sapiensPaper_evidenceWBPaper00041253
Curator_confirmedWBPerson324
Date_last_updated19 Nov 2013 00:00:00
Models_disease_in_annotationWBDOannot00000246
Molecular_infoCorresponding_CDSC16D6.2a
C16D6.2b
C16D6.2c
C16D6.2d
Corresponding_CDS_historyC16D6.2:wp131
Corresponding_transcriptC16D6.2a.1
C16D6.2b.1
C16D6.2b.2
C16D6.2c.1
C16D6.2c.2
C16D6.2d.1
Other_sequenceMI03769
AI438264.1
JI171599.1
MI01326
MIC00702_1
AY882441.1
OVC02861_1
Associated_feature (23)
Experimental_infoRNAi_resultWBRNAi00028971Inferred_automaticallyRNAi_primary
WBRNAi00010863Inferred_automaticallyRNAi_primary
WBRNAi00040729Inferred_automaticallyRNAi_primary
WBRNAi00075424Inferred_automaticallyRNAi_primary
Expr_patternExpr8975
Expr12804
Expr1013004
Expr1144774
Expr2014424
Expr2032665
Drives_constructWBCnstr00013648
WBCnstr00018592
WBCnstr00022791
WBCnstr00033589
Construct_productWBCnstr00022791
WBCnstr00033589
Microarray_results (20)
Expression_cluster (125)
Interaction (27)
Map_infoMapXPosition7.17548
PositivePositive_cloneC16D6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (17)
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