WormBase Tree Display for Gene: WBGene00009330
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WBGene00009330 | SMap | S_parent | Sequence | F32D8 | ||
---|---|---|---|---|---|---|
Identity (6) | ||||||
Gene_info | Biotype | SO:0001217 | ||||
Allele | WBVar01743227 | |||||
WBVar01045493 | ||||||
WBVar01045494 | ||||||
WBVar00469606 | ||||||
WBVar00469607 | ||||||
WBVar01500208 | ||||||
WBVar01500209 | ||||||
WBVar01499316 | ||||||
RNASeq_FPKM (74) | ||||||
GO_annotation | 00066488 | |||||
00066489 | ||||||
00066490 | ||||||
Ortholog (35) | ||||||
Structured_description | Automated_description | Predicted to be involved in mitochondrial proton-transporting ATP synthase complex assembly. Predicted to be located in membrane and mitochondrion. Human ortholog(s) of this gene implicated in mitochondrial complex V (ATP synthase) deficiency nuclear type 2. Is an ortholog of human TMEM70 (transmembrane protein 70). | 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:0060331 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:26050) | |
Molecular_info | Corresponding_CDS | F32D8.5a | ||||
F32D8.5b | ||||||
Corresponding_transcript | F32D8.5a.1 | |||||
F32D8.5b.1 | ||||||
Other_sequence | GW407258.1 | |||||
PSC03624_1 | ||||||
Associated_feature | WBsf647205 | |||||
WBsf647206 | ||||||
WBsf232425 | ||||||
WBsf232426 | ||||||
Experimental_info (7) | ||||||
Map_info | Positive | Positive_clone | F32D8 | Inferred_automatically | From sequence, transcript, pseudogene data | |
Interpolated_map_position | V | 2.8275 | ||||
Reference | WBPaper00041771 | |||||
Method | Gene |