WormBase Tree Display for Gene: WBGene00019061
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WBGene00019061 | SMap | S_parent | Sequence | F58F12 | |||||
---|---|---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||||
Name | Sequence_name | F58F12.1 | |||||||
Molecular_name | F58F12.1 | ||||||||
F58F12.1.1 | |||||||||
CE01976 | |||||||||
Other_name | phi-38 | Person_evidence | WBPerson2582 | ||||||
CELE_F58F12.1 | Accession_evidence | NDB | BX284602 | ||||||
Public_name | F58F12.1 | ||||||||
DB_info | Database (11) | ||||||||
Species | Caenorhabditis elegans | ||||||||
History | Version_change | 1 | 28 May 2004 13:31:01 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
2 | 17 Mar 2005 13:54:35 | WBPerson2970 | Name_change | Other_name | phi-38 | ||||
Status | Live | ||||||||
Gene_info | Biotype | SO:0001217 | |||||||
Allele (20) | |||||||||
RNASeq_FPKM (74) | |||||||||
GO_annotation (17) | |||||||||
Ortholog (38) | |||||||||
Structured_description | Concise_description | F58F12.1 encodes the delta subunit of the soluble, catalytic F1 portion of ATP synthase (mitochondrial respiratory chain [MRC] complex V); RNAi experiments indicate that F58F12.1 activity is essential for embryonic and larval development, as well as for reproduction and normal rates of growth and development. | Paper_evidence | WBPaper00005654 | |||||
WBPaper00006395 | |||||||||
WBPaper00024497 | |||||||||
WBPaper00024944 | |||||||||
WBPaper00025054 | |||||||||
Curator_confirmed | WBPerson1843 | ||||||||
Date_last_updated | 17 Jan 2007 00:00:00 | ||||||||
Automated_description | Predicted to contribute to proton-transporting ATP synthase activity, rotational mechanism. Predicted to be involved in proton motive force-driven ATP synthesis. Located in mitochondrion. Human ortholog(s) of this gene implicated in Alzheimer's disease and mitochondrial complex V (ATP synthase) deficiency nuclear type 5. Is an ortholog of human ATP5F1D (ATP synthase F1 subunit delta). | 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:0070463 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:837) | ||||
DOID:10652 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:837) | ||||||
Molecular_info | Corresponding_CDS | F58F12.1 | |||||||
Corresponding_transcript | F58F12.1.1 | ||||||||
Other_sequence (81) | |||||||||
Associated_feature | WBsf644277 | ||||||||
WBsf716695 | |||||||||
WBsf716994 | |||||||||
WBsf717681 | |||||||||
WBsf717682 | |||||||||
WBsf981209 | |||||||||
WBsf988146 | |||||||||
WBsf221434 | |||||||||
WBsf221435 | |||||||||
Experimental_info | RNAi_result (12) | ||||||||
Expr_pattern | Expr1018730 | ||||||||
Expr1038230 | |||||||||
Expr1152755 | |||||||||
Expr2004402 | |||||||||
Expr2022626 | |||||||||
Drives_construct | WBCnstr00026092 | ||||||||
Construct_product | WBCnstr00026092 | ||||||||
Microarray_results (18) | |||||||||
Expression_cluster (125) | |||||||||
Interaction (120) | |||||||||
Map_info | Positive | Positive_clone | F58F12 | Inferred_automatically | From sequence, transcript, pseudogene data | ||||
Interpolated_map_position | II | -0.365554 | |||||||
Reference | WBPaper00024944 | ||||||||
WBPaper00028999 | |||||||||
WBPaper00038491 | |||||||||
WBPaper00049828 | |||||||||
WBPaper00055090 | |||||||||
WBPaper00061870 | |||||||||
Method | Gene |