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WormBase Tree Display for Gene: WBGene00000440

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Name Class

WBGene00000440SMapS_parentSequenceD1007
IdentityVersion1
NameCGC_nameceh-17Person_evidenceWBPerson83
Sequence_nameD1007.1
Molecular_nameD1007.1
D1007.1.1
CE09036
Other_nameceh-42
CELE_D1007.1Accession_evidenceNDBBX284601
Public_nameceh-17
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:20WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classceh
Allele (25)
Legacy_informationPhox2/Arix1/smox-3 family homeobox gene [info from Burglin 03/98]
StrainWBStrain00035300
WBStrain00035301
WBStrain00035312
WBStrain00008608
WBStrain00052001
RNASeq_FPKM (74)
GO_annotation (18)
Ortholog (26)
Paralog (20)
Structured_descriptionConcise_descriptionceh-17 encodes a phox-2-like homeodomain protein that is a member of the Q50 paired-like class of homeobox proteins and the vertebrate orthologue of Phox2a and Phox2b; that affects ALA and SIA axonal development; ceh-17 affects ALA and SIA antero-posterior axonal growth and navigation, and is expressed in five neurons of the ring ganglia (ALA and the 4 SIAs) with strongest expression in embryos and in L1 stage larvae.Paper_evidenceWBPaper00004283
WBPaper00015614
Curator_confirmedWBPerson48
WBPerson324
Date_last_updated17 Jun 2004 00:00:00
Automated_descriptionEnables DNA-binding transcription activator activity, RNA polymerase II-specific. Involved in axon guidance; positive regulation of transcription by RNA polymerase II; and regulation of axon extension. Located in nucleus. Expressed in DA8; head muscle; head neurons; and somatic nervous system. Human ortholog(s) of this gene implicated in several diseases, including congenital central hypoventilation syndrome; congenital fibrosis of the extraocular muscles 2; and neuroblastoma. Is an ortholog of human PHOX2A (paired like homeobox 2A).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:9256Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9143)
DOID:0060731Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9143)
DOID:769Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:9143)
DOID:0081016Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:691)
Molecular_infoCorresponding_CDSD1007.1
Corresponding_transcriptD1007.1.1
Other_sequence (16)
Associated_featureWBsf978409
Transcription_factorWBTranscriptionFactor000388
Experimental_infoRNAi_resultWBRNAi00084772Inferred_automaticallyRNAi_primary
WBRNAi00003251Inferred_automaticallyRNAi_primary
WBRNAi00030301Inferred_automaticallyRNAi_primary
WBRNAi00043320Inferred_automaticallyRNAi_primary
Expr_patternChronogram57
Chronogram86
Chronogram88
Expr1039
Expr7489
Expr15566
Expr1017681
Expr1147298
Expr2009863
Expr2028103
Drives_constructWBCnstr00001110
WBCnstr00001111
WBCnstr00001122
WBCnstr00006931
WBCnstr00010043
WBCnstr00012633
WBCnstr00037537
WBCnstr00042410
Construct_productWBCnstr00010043
WBCnstr00037537
WBCnstr00039986
WBCnstr00039998
WBCnstr00042410
AntibodyWBAntibody00000299
Microarray_results (18)
Expression_cluster (69)
Interaction (72)
WBProcessWBbiopr:00000044
Map_infoMapIPosition-1.0462Error0.001888
PositivePositive_cloneD1007Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4204
5492
Pseudo_map_position
Reference (43)
Remarkrenamed by T.Burglin 1/99. See also wbg15.5p29 [030204 ck1]
Map 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