WormBase Tree Display for Gene: WBGene00000097
expand all nodes | collapse all nodes | view schema
WBGene00000097 | SMap | S_parent | Sequence | F58E10 | |||
---|---|---|---|---|---|---|---|
Identity (6) | |||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | aip | ||||||
Allele (11) | |||||||
Strain | WBStrain00035638 | ||||||
WBStrain00036456 | |||||||
RNASeq_FPKM (74) | |||||||
GO_annotation | 00102182 | ||||||
00102183 | |||||||
00102184 | |||||||
00102185 | |||||||
00102186 | |||||||
00102187 | |||||||
00102188 | |||||||
00102189 | |||||||
00102190 | |||||||
00106777 | |||||||
Ortholog (39) | |||||||
Structured_description | Concise_description | aip-1 encodes an AN-1-like zinc finger-containing protein homologous to arsenite-inducible RNA-associated protein (AIRAP), conserved among C. elegans, Drosophila, and mammals; like AIRAP itself, AIP-1 protects cells from arsenite toxicity; AIP-1 is a predicted RNA binding protein that may function in ubiquitin-mediated proteolysis following arsenite treatment; AIP-1 does not appear to be essential for viability, but is expressed at high levels in hypodermal and intestinal cells following such treatment. | Paper_evidence | WBPaper00004641 | |||
Curator_confirmed | WBPerson1843 | ||||||
Date_last_updated | 17 Jun 2004 00:00:00 | ||||||
Automated_description | Predicted to enable zinc ion binding activity. Involved in cellular response to misfolded protein and response to arsenic-containing substance. Located in cytoplasm and nucleus. Expressed in body wall musculature; excretory cell; pharynx; and somatic gonad. Is an ortholog of human ZFAND2A (zinc finger AN1-type containing 2A) and ZFAND2B (zinc finger AN1-type containing 2B). | 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 | ||||||
Modifies_disease | DOID:10652 | ||||||
Modifies_disease_in_annotation | WBDOannot00000387 | ||||||
Molecular_info | Corresponding_CDS | F58E10.4 | |||||
Corresponding_transcript | F58E10.4.1 | ||||||
Other_sequence (14) | |||||||
Associated_feature | WBsf216751 | ||||||
WBsf216752 | |||||||
WBsf647506 | |||||||
WBsf661074 | |||||||
WBsf982036 | |||||||
WBsf1001915 | |||||||
WBsf232857 | |||||||
Experimental_info (9) | |||||||
Map_info | Map | V | Position | 5.91965 | Error | 0.0241 | |
Positive | Positive_clone | F58E10 | Inferred_automatically | From CDS info | |||
From sequence, transcript, pseudogene data | |||||||
Mapping_data | Multi_point | 4149 | |||||
4287 | |||||||
4288 | |||||||
Pseudo_map_position | |||||||
Reference (14) | |||||||
Remark | Sequence connection from [Sok J, Ron D] | ||||||
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 |