WormBase Tree Display for Gene: WBGene00000951
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| WBGene00000951 | SMap | S_parent | Sequence | K03B8 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 1 | |||||||
| Name | CGC_name | deg-3 | Person_evidence | WBPerson95 | |||||
| Sequence_name | K03B8.9 | ||||||||
| Molecular_name | K03B8.9 | ||||||||
| K03B8.9.1 | |||||||||
| CE06083 | |||||||||
| K03B8.9.2 | |||||||||
| Other_name | CELE_K03B8.9 | Accession_evidence | NDB | BX284605 | |||||
| Public_name | deg-3 | ||||||||
| DB_info | Database | AceView | gene | 5L894 | |||||
| WormQTL | gene | WBGene00000951 | |||||||
| WormFlux | gene | WBGene00000951 | |||||||
| NDB | locus_tag | CELE_K03B8.9 | |||||||
| Panther | gene | CAEEL|WormBase=WBGene00000951|UniProtKB=P54244 | |||||||
| family | PTHR18945 | ||||||||
| NCBI | gene | 3565200 | |||||||
| RefSeq | protein | NM_001392614.1 | |||||||
| SwissProt | UniProtAcc | P54244 | |||||||
| UniProt_GCRP | UniProtAcc | P54244 | |||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 07 Apr 2004 11:29:22 | WBPerson1971 | Event | Imported | Initial conversion from geneace | ||
| Status | Live | ||||||||
| Gene_info (11) | |||||||||
| Disease_info | Experimental_model | DOID:1289 | Homo sapiens | Paper_evidence | WBPaper00002167 | ||||
| WBPaper00032364 | |||||||||
| Curator_confirmed | WBPerson324 | ||||||||
| WBPerson38202 | |||||||||
| Date_last_updated | 22 May 2018 00:00:00 | ||||||||
| Disease_relevance | Defects in human sodium channel proteins cause several disorders including hyperkalemic periodic paralysis and paramyotonia congenita; Chloride channel defects produce cystic fibrosis and acetylcholine receptor defects underlie the congenital myasthenic syndromes. | Homo sapiens | Curator_confirmed | WBPerson324 | |||||
| Date_last_updated | 25 Nov 2014 00:00:00 | ||||||||
| Models_disease_asserted | WBDOannot00000334 | ||||||||
| WBDOannot00000526 | |||||||||
| Molecular_info | Corresponding_CDS | K03B8.9 | |||||||
| Corresponding_transcript | K03B8.9.1 | ||||||||
| K03B8.9.2 | |||||||||
| Other_sequence (22) | |||||||||
| Associated_feature | WBsf234533 | ||||||||
| Experimental_info | RNAi_result | WBRNAi00102749 | Inferred_automatically | RNAi_primary | |||||
| WBRNAi00016526 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00066377 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00049804 | Inferred_automatically | RNAi_primary | |||||||
| WBRNAi00027652 | Inferred_automatically | RNAi_primary | |||||||
| Expr_pattern | Expr224 | ||||||||
| Expr9315 | |||||||||
| Expr1013101 | |||||||||
| Expr1030591 | |||||||||
| Expr1153524 | |||||||||
| Expr2010844 | |||||||||
| Expr2029082 | |||||||||
| Drives_construct | WBCnstr00010719 | ||||||||
| WBCnstr00013896 | |||||||||
| WBCnstr00037183 | |||||||||
| Construct_product | WBCnstr00014763 | ||||||||
| WBCnstr00037183 | |||||||||
| Antibody | WBAntibody00001595 | ||||||||
| Microarray_results (20) | |||||||||
| Expression_cluster (150) | |||||||||
| Interaction (43) | |||||||||
| Map_info | Map | V | Position | 3.08425 | Error | 0.002323 | |||
| Well_ordered | |||||||||
| Positive | Positive_clone | K03B8 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| T21D1 | |||||||||
| Mapping_data | 2_point | 6220 | |||||||
| 7052 | |||||||||
| Multi_point | 2781 | ||||||||
| 2782 | |||||||||
| 3788 | |||||||||
| 3971 | |||||||||
| 4255 | |||||||||
| 4230 | |||||||||
| Reference (90) | |||||||||
| Remark | mutation isolated from 'nT1(dm)', a dominant unc and recessive lethal derivative of nT1. u662 is not recessive lethal. | ||||||||
| In an operon with des-2. email 20 from wen chen | |||||||||
| Method | Gene |
