WormBase Tree Display for Gene: WBGene00007216
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WBGene00007216 | SMap | S_parent | Sequence | C01A2 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 1 | |||||||
Name | Sequence_name | C01A2.4 | |||||||
Molecular_name | C01A2.4 | ||||||||
C01A2.4.1 | |||||||||
CE34247 | |||||||||
Other_name | CELE_C01A2.4 | Accession_evidence | NDB | BX284601 | |||||
Public_name | C01A2.4 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 26 May 2004 16:54:47 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Allele (51) | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00026732 | ||||||||
00026733 | |||||||||
00026734 | |||||||||
00026735 | |||||||||
00026736 | |||||||||
00026737 | |||||||||
00026738 | |||||||||
00115429 | |||||||||
Contained_in_operon | CEOP1696 | ||||||||
Ortholog (30) | |||||||||
Paralog | WBGene00017735 | Caenorhabditis elegans | From_analysis | Panther | |||||
WormBase-Compara | |||||||||
WBGene00012903 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
WBGene00020866 | Caenorhabditis elegans | From_analysis | Panther | ||||||
WormBase-Compara | |||||||||
Structured_description | Automated_description | Predicted to be involved in endosome transport via multivesicular body sorting pathway; late endosome to vacuole transport; and protein transport. Predicted to be located in multivesicular body. Predicted to be part of ESCRT III complex. Human ortholog(s) of this gene implicated in amyotrophic lateral sclerosis and chromosome 3-linked frontotemporal dementia. Is an ortholog of human CHMP2B (charged multivesicular body protein 2B). | 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:0111227 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:24537) | ||||
DOID:332 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:24537) | ||||||
DOID:9255 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:24537) | ||||||
Molecular_info | Corresponding_CDS | C01A2.4 | |||||||
Corresponding_CDS_history | C01A2.4:wp103 | ||||||||
Corresponding_transcript | C01A2.4.1 | ||||||||
Other_sequence (26) | |||||||||
Associated_feature | WBsf985853 | ||||||||
WBsf1011065 | |||||||||
WBsf218724 | |||||||||
Experimental_info | RNAi_result | WBRNAi00116898 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00076063 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00002872 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00039230 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00028253 | Inferred_automatically | RNAi_primary | |||||||
WBRNAi00110711 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Expr1014765 | ||||||||
Expr1033110 | |||||||||
Expr1143371 | |||||||||
Expr2000262 | |||||||||
Expr2018483 | |||||||||
Drives_construct | WBCnstr00033914 | ||||||||
Construct_product | WBCnstr00033914 | ||||||||
Microarray_results (20) | |||||||||
Expression_cluster (131) | |||||||||
Interaction | WBInteraction000388006 | ||||||||
WBInteraction000544439 | |||||||||
WBInteraction000577242 | |||||||||
WBInteraction000584151 | |||||||||
WBInteraction000584445 | |||||||||
Map_info | Positive | Positive_clone | C01A2 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
Interpolated_map_position | I | 19.558 | |||||||
Reference | WBPaper00038491 | ||||||||
WBPaper00055090 | |||||||||
WBPaper00064339 | |||||||||
Method | Gene |