WormBase Tree Display for Gene: WBGene00001432
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WBGene00001432 | SMap | S_parent | Sequence | CHROMOSOME_I | |||
---|---|---|---|---|---|---|---|
Identity (6) | |||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | fkb | ||||||
Allele (38) | |||||||
Legacy_information | [Page AP] B0511.1 No mutants known. | ||||||
RNASeq_FPKM (74) | |||||||
GO_annotation | 00036419 | ||||||
00036420 | |||||||
00036421 | |||||||
00036422 | |||||||
00036423 | |||||||
00036424 | |||||||
00108698 | |||||||
Ortholog (43) | |||||||
Paralog | WBGene00001426 | Caenorhabditis elegans | From_analysis | WormBase-Compara | |||
WBGene00001427 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
WBGene00001428 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
WBGene00001429 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
WBGene00001430 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
WBGene00001431 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
WBGene00001433 | Caenorhabditis elegans | From_analysis | WormBase-Compara | ||||
Structured_description | Concise_description | fkb-7 encodes a peptidylprolyl cis/trans isomerase homologous to mammalian FK506-binding proteins; by homology, FKB-7 could function in a number of different processes including protein folding, signal transduction, and regulation of muscle contraction; however, as loss of fkb-7 function via RNA-mediated interference (RNAi) does not result in any obvious abnormalities, the precise role of FKB-7 in C. elegans development and/or behavior is not yet known. | Paper_evidence | WBPaper00004285 | |||
WBPaper00004402 | |||||||
Curator_confirmed | WBPerson1843 | ||||||
Date_last_updated | 17 Jun 2004 00:00:00 | ||||||
Automated_description | Predicted to enable peptidyl-prolyl cis-trans isomerase activity. Human ortholog(s) of this gene implicated in Ehlers-Danlos syndrome kyphoscoliotic type 2. Is an ortholog of human FKBP14 (FKBP prolyl isomerase 14) and FKBP7 (FKBP prolyl isomerase 7). | 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:0080735 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:18625) | ||
Molecular_info | Corresponding_CDS | B0511.1 | |||||
Corresponding_transcript | B0511.1.1 | ||||||
Other_sequence (27) | |||||||
Associated_feature | WBsf643705 | ||||||
WBsf656893 | |||||||
WBsf985054 | |||||||
WBsf218472 | |||||||
Experimental_info | RNAi_result | WBRNAi00003073 | Inferred_automatically | RNAi_primary | |||
WBRNAi00116495 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00115760 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00002859 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00076058 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00039137 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00115895 | Inferred_automatically | RNAi_primary | |||||
Expr_pattern | Expr16139 | ||||||
Expr1022076 | |||||||
Expr1030857 | |||||||
Expr1143294 | |||||||
Expr2011801 | |||||||
Expr2030039 | |||||||
Drives_construct | WBCnstr00036953 | ||||||
Construct_product | WBCnstr00036953 | ||||||
Microarray_results (20) | |||||||
Expression_cluster (248) | |||||||
Interaction (36) | |||||||
Map_info | Map | I | Position | 5.06033 | Error | 0.000114 | |
Positive | Positive_clone | B0511 | Inferred_automatically | From sequence, transcript, pseudogene data | |||
Pseudo_map_position | |||||||
Reference | WBPaper00004285 | ||||||
WBPaper00026884 | |||||||
WBPaper00038491 | |||||||
WBPaper00055090 | |||||||
WBPaper00062388 | |||||||
WBPaper00064339 | |||||||
Remark | ACeDB prediction of first exon is incorrect -- see intronerator entry g-I-1963 | ||||||
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 |