WormBase Tree Display for Gene: WBGene00009002
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WBGene00009002 | SMap | S_parent | Sequence | F21C3 | |||
---|---|---|---|---|---|---|---|
Identity (6) | |||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | hint | ||||||
Allele (18) | |||||||
Strain | WBStrain00035947 | ||||||
WBStrain00055400 | |||||||
RNASeq_FPKM (74) | |||||||
GO_annotation | 00048121 | ||||||
00048122 | |||||||
00048123 | |||||||
00048124 | |||||||
00116800 | |||||||
Contained_in_operon | CEOP1384 | ||||||
Ortholog (37) | |||||||
Structured_description | Automated_description | Predicted to enable hydrolase activity. Predicted to be involved in purine ribonucleotide catabolic process. Predicted to be located in cytoplasm and nucleus. Human ortholog(s) of this gene implicated in Gamstorp-Wohlfart syndrome. Is an ortholog of human HINT1 (histidine triad nucleotide binding protein 1). | 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:0050526 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4912) | ||
Molecular_info | Corresponding_CDS | F21C3.3 | |||||
Corresponding_transcript | F21C3.3.1 | ||||||
F21C3.3.2 | |||||||
Other_sequence (56) | |||||||
Associated_feature | WBsf219727 | ||||||
WBsf219728 | |||||||
Experimental_info (7) | |||||||
Map_info | Map | I | Position | 1.87133 | Error | 0.000432 | |
Positive | Positive_clone | F21C3 | Inferred_automatically | From sequence, transcript, pseudogene data | |||
Mapping_data | Multi_point | 4953 | |||||
5056 | |||||||
5087 | |||||||
Pseudo_map_position | |||||||
Reference | WBPaper00038491 | ||||||
WBPaper00055090 | |||||||
WBPaper00064339 | |||||||
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 |