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: WBGene00000561

expand all nodes | collapse all nodes | view schema

Name Class

WBGene00000561EvidencePaper_evidenceWBPaper00004409
SMapS_parentSequenceC34E10
IdentityVersion1
NameCGC_namecnd-1Person_evidenceWBPerson105
WBPerson293
Sequence_nameC34E10.7
Molecular_nameC34E10.7
C34E10.7.1
CE01187
Other_namehlh-5Person_evidenceWBPerson346
C34E10.dCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
C34E10Paper_evidenceWBPaper00027608
CeNDPaper_evidenceWBPaper00027608
CELE_C34E10.7Accession_evidenceNDBBX284603
Public_namecnd-1
DB_infoDatabaseAceViewgene3G328
WormQTLgeneWBGene00000561
WormFluxgeneWBGene00000561
OMIMdisease125853
606394
gene601724
601725
NDBlocus_tagCELE_C34E10.7
PanthergeneCAEEL|WormBase=WBGene00000561|UniProtKB=P46581
familyPTHR19290
NCBIgene183212
RefSeqproteinNM_001392092.1
SwissProtUniProtAccP46581
UniProt_GCRPUniProtAccP46581
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:21WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classcnd
Allele (58)
StrainWBStrain00029627
WBStrain00029628
WBStrain00036693
WBStrain00036763
WBStrain00005364
WBStrain00029967
RNASeq_FPKM (74)
GO_annotation (17)
Ortholog (57)
ParalogWBGene00001957Caenorhabditis elegansFrom_analysisTreeFam
WBGene00003595Caenorhabditis elegansFrom_analysisTreeFam
WormBase-Compara
WBGene00001953Caenorhabditis elegansFrom_analysisTreeFam
WBGene00001960Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00001961Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00003018Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00009540Caenorhabditis elegansFrom_analysisWormBase-Compara
WBGene00013665Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionConcise_descriptioncnd-1 encodes a basic helix-loop-helix protein that is most closely related to the vertebrate NeuroD transcription factors; during development, CND-1 is predicted to function as a transcriptional regulator whose activity is required for several aspects of motor neuron fate specification, including cell division patterns, proper spatiotemporal expression of fate-specific markers, and normal axonal morphology and pathfinding; CND-1::GFP expression begins in early embryogenesis (<20 cells) in four AB descendants and then continues in mitotically active AB-derived neuronal precursors, unidentified nuclei during gastrulation and enclosure, and postmitotic neurons in the head and ventral cord; at hatching CND-1::GFP expression is visible in ventral cord neurons, but this expression disappears completely by the end of the first larval stage; CND-1::GFP does not appear to be expressed in any non-neuronal ectodermal cells, as its expression does not overlap with that of LIN-26.Paper_evidenceWBPaper00004409
Curator_confirmedWBPerson1843
WBPerson1823
WBPerson567
Date_last_updated11 May 2006 00:00:00
Automated_descriptionPredicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and E-box binding activity. Involved in axonal fasciculation and negative regulation of gliogenesis. Located in nucleus. Expressed in several structures, including ABalpapaa; ABalppapa; motor neurons; neuroblasts; and somatic nervous system. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 72; glucose metabolism disease (multiple); and obesity. Is an ortholog of several human genes including NEUROD1 (neuronal differentiation 1); NEUROD2 (neuronal differentiation 2); and NEUROD4 (neuronal differentiation 4).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:9744Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7762)
DOID:4195Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7762)
DOID:10603Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7762)
DOID:9970Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7762)
DOID:9352Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7762)
DOID:0111104Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7762)
DOID:0112208Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7763)
Disease_relevanceIn humans, mutations in Neurogenic Differentiation 1 (NeuroD1) have been implicated in Diabetes Mellitus, Type II and Maturity-onset diabetes of the young, type VI; in elegans, cnd-1, seems to have combined the function of several vertebrate neurogenic bHLH proteins, and is required for the proper fate specification and terminal differentiation of motor neurons.Homo sapiensPaper_evidenceWBPaper00004409
Accession_evidenceOMIM606394
125853
601724
Curator_confirmedWBPerson324
Date_last_updated06 Sep 2013 00:00:00
Molecular_infoCorresponding_CDSC34E10.7
Corresponding_transcriptC34E10.7.1
Other_sequenceDviv_isotig35392
Dviv_isotig31167
JI178639.1
Tcol_isotig15910
Associated_featureWBsf651039
WBsf666900
WBsf978355
WBsf992340
WBsf992341
WBsf226653
Transcription_factorWBTranscriptionFactor000076
WBTranscriptionFactor000060
Experimental_infoRNAi_resultWBRNAi00107382Inferred_automaticallyRNAi_primary
WBRNAi00041895Inferred_automaticallyRNAi_primary
WBRNAi00029528Inferred_automaticallyRNAi_primary
WBRNAi00005521Inferred_automaticallyRNAi_primary
WBRNAi00066068Inferred_automaticallyRNAi_primary
WBRNAi00011606Inferred_automaticallyRNAi_primary
Expr_pattern (18)
Drives_constructWBCnstr00004609
WBCnstr00004610
WBCnstr00004611
WBCnstr00013822
WBCnstr00015211
WBCnstr00015212
WBCnstr00015213
WBCnstr00037451
WBCnstr00042892
WBCnstr00042894
Construct_productWBCnstr00013822
WBCnstr00015371
WBCnstr00015372
WBCnstr00016754
WBCnstr00016967
WBCnstr00021504
WBCnstr00037451
Regulate_expr_clusterWBPaper00059932:cnd-1(ju29)_downregulated
WBPaper00059932:cnd-1(ju29)_upregulated
Microarray_results (18)
Expression_cluster (159)
Interaction (102)
Map_infoMapIIIPosition-1.85688Error0.001135
PositivePositive_cloneC34E10Inferred_automaticallyFrom sequence, transcript, pseudogene data
ZC129
Mapping_data2_point7160
Multi_point4094
Pos_neg_data10730
ReferenceWBPaper00004409
WBPaper00005455
WBPaper00006120
WBPaper00006397
WBPaper00015656
WBPaper00017088
WBPaper00017224
WBPaper00017459
WBPaper00018453
WBPaper00019775
WBPaper00022122
WBPaper00022152
WBPaper00022794
WBPaper00024719
WBPaper00027299
WBPaper00027309
WBPaper00027608
WBPaper00028150
WBPaper00028984
WBPaper00031983
WBPaper00034710
WBPaper00034761
WBPaper00037020
WBPaper00038491
WBPaper00039730
WBPaper00043594
WBPaper00047143
WBPaper00047936
WBPaper00052395
WBPaper00052430
WBPaper00052496
WBPaper00052676
WBPaper00055090
WBPaper00057866
WBPaper00059932
WBPaper00059989
WBPaper00061738
WBPaper00064339
RemarkPostitive method is cosmid rescuePaper_evidenceWBPaper00004409
MethodGene