WormBase Tree Display for Gene: WBGene00000440
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WBGene00000440 | SMap | S_parent | Sequence | D1007 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 1 | |||||||
Name | CGC_name | ceh-17 | Person_evidence | WBPerson83 | |||||
Sequence_name | D1007.1 | ||||||||
Molecular_name | D1007.1 | ||||||||
D1007.1.1 | |||||||||
CE09036 | |||||||||
Other_name | ceh-42 | ||||||||
CELE_D1007.1 | Accession_evidence | NDB | BX284601 | ||||||
Public_name | ceh-17 | ||||||||
DB_info | Database (12) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 07 Apr 2004 11:29:20 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | ceh | ||||||||
Allele (25) | |||||||||
Legacy_information | Phox2/Arix1/smox-3 family homeobox gene [info from Burglin 03/98] | ||||||||
Strain | WBStrain00035300 | ||||||||
WBStrain00035301 | |||||||||
WBStrain00035312 | |||||||||
WBStrain00008608 | |||||||||
WBStrain00052001 | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation (18) | |||||||||
Ortholog (26) | |||||||||
Paralog (20) | |||||||||
Structured_description | Concise_description | ceh-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_evidence | WBPaper00004283 | |||||
WBPaper00015614 | |||||||||
Curator_confirmed | WBPerson48 | ||||||||
WBPerson324 | |||||||||
Date_last_updated | 17 Jun 2004 00:00:00 | ||||||||
Automated_description | Enables 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_evidence | WBPaper00065943 | ||||||
Curator_confirmed | WBPerson324 | ||||||||
WBPerson37462 | |||||||||
Inferred_automatically | This description was generated automatically by a script based on data from the WS291 version of WormBase | ||||||||
Date_last_updated | 29 Nov 2023 00:00:00 | ||||||||
Disease_info | Potential_model | DOID:9256 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9143) | ||||
DOID:0060731 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9143) | ||||||
DOID:769 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:9143) | ||||||
DOID:0081016 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:691) | ||||||
Molecular_info | Corresponding_CDS | D1007.1 | |||||||
Corresponding_transcript | D1007.1.1 | ||||||||
Other_sequence (16) | |||||||||
Associated_feature | WBsf978409 | ||||||||
Transcription_factor | WBTranscriptionFactor000388 | ||||||||
Experimental_info | RNAi_result | WBRNAi00084772 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00003251 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00030301 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00043320 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Chronogram57 | ||||||||
Chronogram86 | |||||||||
Chronogram88 | |||||||||
Expr1039 | |||||||||
Expr7489 | |||||||||
Expr15566 | |||||||||
Expr1017681 | |||||||||
Expr1147298 | |||||||||
Expr2009863 | |||||||||
Expr2028103 | |||||||||
Drives_construct | WBCnstr00001110 | ||||||||
WBCnstr00001111 | |||||||||
WBCnstr00001122 | |||||||||
WBCnstr00006931 | |||||||||
WBCnstr00010043 | |||||||||
WBCnstr00012633 | |||||||||
WBCnstr00037537 | |||||||||
WBCnstr00042410 | |||||||||
Construct_product | WBCnstr00010043 | ||||||||
WBCnstr00037537 | |||||||||
WBCnstr00039986 | |||||||||
WBCnstr00039998 | |||||||||
WBCnstr00042410 | |||||||||
Antibody | WBAntibody00000299 | ||||||||
Microarray_results (18) | |||||||||
Expression_cluster (69) | |||||||||
Interaction (72) | |||||||||
WBProcess | WBbiopr:00000044 | ||||||||
Map_info | Map | I | Position | -1.0462 | Error | 0.001888 | |||
Positive | Positive_clone | D1007 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
Mapping_data | Multi_point | 4204 | |||||||
5492 | |||||||||
Pseudo_map_position | |||||||||
Reference (43) | |||||||||
Remark | renamed 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 | ||||||||
Method | Gene |