WormBase Tree Display for Gene: WBGene00012950
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WBGene00012950 | SMap | S_parent | Sequence | Y47H9C | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | CGC_name | eif-2Bbeta | Person_evidence | WBPerson2266 | |||||
Sequence_name | Y47H9C.7 | ||||||||
Molecular_name | Y47H9C.7 | ||||||||
Y47H9C.7.1 | |||||||||
CE20267 | |||||||||
Other_name | CELE_Y47H9C.7 | Accession_evidence | NDB | BX284601 | |||||
Public_name | eif-2Bbeta | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 26 May 2004 16:54:54 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
2 | 09 Jan 2017 15:00:31 | WBPerson2970 | Name_change | CGC_name | eif-2Bbeta | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Gene_class | eif | ||||||||
Allele (61) | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation | 00103346 | ||||||||
00103347 | |||||||||
00103348 | |||||||||
00103349 | |||||||||
00103350 | |||||||||
00103351 | |||||||||
00119917 | |||||||||
Ortholog (37) | |||||||||
Paralog | WBGene00007236 | Caenorhabditis elegans | From_analysis | WormBase-Compara | |||||
WBGene00008670 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
WBGene00014221 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||||
Structured_description | Concise_description | Y47H9C.7 is orthologous to the human gene EUKARYOTIC TRANSLATION INITIATION FACTOR 2B, SUBUNIT 2 (BETA, 39KD) (EIF2B2; OMIM:606454), which when mutated leads to disease. | Curator_confirmed | WBPerson1823 | |||||
WBPerson567 | |||||||||
Date_last_updated | 06 Aug 2004 00:00:00 | ||||||||
Automated_description | Predicted to enable translation initiation factor activity. Predicted to contribute to guanyl-nucleotide exchange factor activity. Predicted to be involved in translational initiation. Predicted to be part of eukaryotic translation initiation factor 2B complex. Human ortholog(s) of this gene implicated in leukoencephalopathy with vanishing white matter 2. Is an ortholog of human EIF2B2 (eukaryotic translation initiation factor 2B subunit beta). | 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:0070373 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3258) | ||||
DOID:0060868 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:3258) | ||||||
Molecular_info | Corresponding_CDS | Y47H9C.7 | |||||||
Corresponding_transcript | Y47H9C.7.1 | ||||||||
Other_sequence | MH07180 | ||||||||
HBC04511_1 | |||||||||
ES408816.1 | |||||||||
Hbac_isotig02304 | |||||||||
Oden_isotig10408 | |||||||||
Acan_isotig15230 | |||||||||
Oden_isotig10407 | |||||||||
FK800800.1 | |||||||||
Tcol_isotig10627 | |||||||||
CBC10110_1 | |||||||||
Associated_feature | WBsf649638 | ||||||||
WBsf220374 | |||||||||
Experimental_info | RNAi_result (26) | ||||||||
Expr_pattern | Expr1014092 | ||||||||
Expr1035743 | |||||||||
Expr1160303 | |||||||||
Expr2011244 | |||||||||
Expr2029480 | |||||||||
Microarray_results (19) | |||||||||
Expression_cluster (98) | |||||||||
Interaction (87) | |||||||||
Map_info | Positive | Positive_clone | Y47H9C | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
Interpolated_map_position | I | 12.9065 | |||||||
Reference | WBPaper00027281 | ||||||||
WBPaper00038491 | |||||||||
WBPaper00055090 | |||||||||
WBPaper00064339 | |||||||||
Method | Gene |