WormBase Tree Display for Gene: WBGene00017282
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WBGene00017282 | SMap | S_parent | Sequence | F09E5 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | algn-2 | Person_evidence | WBPerson261 | |||||
Sequence_name | F09E5.2 | ||||||||
Molecular_name | F09E5.2 | ||||||||
F09E5.2.1 | |||||||||
CE32364 | |||||||||
Other_name | CELE_F09E5.2 | Accession_evidence | NDB | BX284602 | |||||
Public_name | algn-2 | ||||||||
DB_info | Database (13) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 28 May 2004 13:30:58 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
2 | 29 Apr 2015 12:07:40 | WBPerson2970 | Name_change | CGC_name | algn-2 | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | algn | ||||||||
Allele (22) | |||||||||
Strain | WBStrain00051274 | ||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation (15) | |||||||||
Contained_in_operon | CEOP2168 | ||||||||
Ortholog (41) | |||||||||
Paralog | WBGene00044623 | Caenorhabditis elegans | From_analysis | Panther | |||||
WormBase-Compara | |||||||||
WBGene00008431 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
WBGene00015162 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
Structured_description | Automated_description | Predicted to enable alpha-1,3-mannosyltransferase activity. Predicted to be involved in oligosaccharide-lipid intermediate biosynthetic process. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation Ii and congenital myasthenic syndrome 14. Is an ortholog of human ALG2 (ALG2 alpha-1,3/1,6-mannosyltransferase). | 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:0110669 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:23159) | ||||
DOID:0080561 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:23159) | ||||||
Molecular_info | Corresponding_CDS | F09E5.2 | |||||||
Corresponding_CDS_history | F09E5.2:wp88 | ||||||||
Corresponding_transcript | F09E5.2.1 | ||||||||
Other_sequence | MPC00358_1 | ||||||||
HBC11388_1 | |||||||||
Dviv_isotig15133 | |||||||||
EX011322.1 | |||||||||
MP01369 | |||||||||
CBC05573_1 | |||||||||
RSC04390_1 | |||||||||
CGC00667_1 | |||||||||
Associated_feature | WBsf657588 | ||||||||
WBsf221264 | |||||||||
Experimental_info | RNAi_result (16) | ||||||||
Expr_pattern | Expr1025065 | ||||||||
Expr1037424 | |||||||||
Expr1148095 | |||||||||
Expr2009297 | |||||||||
Expr2027534 | |||||||||
Drives_construct | WBCnstr00027427 | ||||||||
WBCnstr00042151 | |||||||||
Construct_product | WBCnstr00027427 | ||||||||
WBCnstr00042151 | |||||||||
Microarray_results (15) | |||||||||
Expression_cluster (59) | |||||||||
Interaction (41) | |||||||||
Map_info | Map | II | Position | -1.78634 | |||||
Positive | Positive_clone | F09E5 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
Pseudo_map_position | |||||||||
Reference | WBPaper00038491 | ||||||||
WBPaper00045573 | |||||||||
WBPaper00048289 | |||||||||
WBPaper00048382 | |||||||||
WBPaper00055090 | |||||||||
WBPaper00060662 | |||||||||
WBPaper00062737 | |||||||||
Remark | 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 |