WormBase Tree Display for Gene: WBGene00017770
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WBGene00017770 | SMap | S_parent | Sequence | F25B4 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 1 | |||||||
Name | Sequence_name | F25B4.7 | |||||||
Molecular_name | F25B4.7 | ||||||||
F25B4.7.1 | |||||||||
CE35287 | |||||||||
Other_name | CELE_F25B4.7 | Accession_evidence | NDB | BX284605 | |||||
Public_name | F25B4.7 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 28 May 2004 13:30:59 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Allele (24) | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation (14) | |||||||||
Ortholog (50) | |||||||||
Paralog (35) | |||||||||
Structured_description | Automated_description | Predicted to enable ATP:ADP antiporter activity. Predicted to be involved in negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in Alzheimer's disease; autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 2; facioscapulohumeral muscular dystrophy; intrinsic cardiomyopathy (multiple); and mitochondrial DNA depletion syndrome (multiple). Is an ortholog of human SLC25A4 (solute carrier family 25 member 4); SLC25A5 (solute carrier family 25 member 5); and SLC25A6 (solute carrier family 25 member 6). | 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:10652 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||
DOID:0110429 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||||
DOID:0080335 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||||
DOID:699 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||||
DOID:11984 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||||
DOID:11727 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||||
DOID:0111517 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||||
DOID:12558 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||||
DOID:0080130 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:10990) | ||||||
Molecular_info (5) | |||||||||
Experimental_info | RNAi_result | WBRNAi00013849 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00045470 | Inferred_automatically | RNAi_primary | |||||||
Expr_pattern | Expr1011362 | ||||||||
Expr1037634 | |||||||||
Expr1149389 | |||||||||
Expr2002945 | |||||||||
Expr2021161 | |||||||||
Drives_construct | WBCnstr00027033 | ||||||||
Construct_product | WBCnstr00027033 | ||||||||
Microarray_results (26) | |||||||||
Expression_cluster (99) | |||||||||
Interaction (14) | |||||||||
Map_info | Positive | Positive_clone | F25B4 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
Interpolated_map_position | V | -1.24052 | |||||||
Reference | WBPaper00038491 | ||||||||
WBPaper00055090 | |||||||||
WBPaper00062301 | |||||||||
Method | Gene |