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WormBase Tree Display for Gene: WBGene00003654

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Name Class

WBGene00003654EvidencePaper_evidenceWBPaper00003416
SMapS_parentSequenceC45E1
IdentityVersion1
NameCGC_namenhr-64Person_evidenceWBPerson600
Sequence_nameC45E1.1
Molecular_nameC45E1.1a
C45E1.1a.1
CE39696
C45E1.1b
CE39697
C45E1.1c
CE52156
C45E1.1a.2
C45E1.1b.1
C45E1.1c.1
Other_nameCELE_C45E1.1Accession_evidenceNDBBX284601
Public_namenhr-64
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classnhr
Allele (197)
StrainWBStrain00032288
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (44)
Paralog (42)
Structured_descriptionConcise_descriptionnhr-64 encodes a conserved nuclear receptor that is a member of the NR2 subfamily of nuclear receptors that contains Drosophila and human HNF4 (OMIM:600281, mutations in human HNF4A are associated with Type I MODY (maturity-onset diabetes of the young)); by homology, NHR-64 is predicted to function as a transcription factor that may activate or repress transcription in response to a hormonal signal; however, as loss of nhr-64 activity via RNAi does not result in any obvious abnormalities, the precise role of NHR-64 in C. elegans development and/or behavior is not yet known; nhr-64 is broadly expressed and detected in anterior and posterior neurons, the ventral nerve cord, the pharynx, gut, and hypodermis.Paper_evidenceWBPaper00006412
Curator_confirmedWBPerson1843
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionPredicted to enable RNA polymerase II cis-regulatory region sequence-specific DNA binding activity and nuclear receptor activity. Predicted to be involved in cell differentiation and regulation of transcription by RNA polymerase II. Predicted to be located in nucleus. Expressed in hypodermis; intestine; neurons; and pharynx. Human ortholog(s) of this gene implicated in several diseases, including Fanconi renotubular syndrome 4; glucose metabolism disease (multiple); and liver disease (multiple). Is an ortholog of human HNF4A (hepatocyte nuclear factor 4 alpha) and HNF4G (hepatocyte nuclear factor 4 gamma).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:0111099Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5024)
DOID:13809Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5024)
DOID:9993Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5024)
DOID:9352Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5024)
DOID:1686Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5024)
DOID:5082Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5024)
DOID:684Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5024)
DOID:0080760Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:5024)
Molecular_infoCorresponding_CDSC45E1.1a
C45E1.1b
C45E1.1c
Corresponding_CDS_historyC45E1.1a:wp154
C45E1.1b:wp154
Corresponding_transcriptC45E1.1a.1
C45E1.1a.2
C45E1.1b.1
C45E1.1c.1
Other_sequence (44)
Associated_featureWBsf656104
WBsf716912
WBsf717472
WBsf983060
WBsf983061
WBsf983062
WBsf983063
WBsf1009453
WBsf1009454
WBsf217365
Transcription_factorWBTranscriptionFactor000193
Experimental_infoRNAi_result (21)
Expr_patternExpr2866
Expr1017257
Expr1031695
Expr1146511
Expr2014215
Expr2032456
Drives_constructWBCnstr00010996
Construct_productWBCnstr00016569
Microarray_results (25)
Expression_cluster (94)
Interaction (35)
Map_infoMapIPosition-4.47689Error0.002016
PositivePositive_cloneC45E1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4749
Pseudo_map_position
ReferenceWBPaper00006412
WBPaper00027288
WBPaper00027309
WBPaper00036075
WBPaper00038491
WBPaper00044077
WBPaper00055090
WBPaper00059191
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