WormBase Tree Display for Gene: WBGene00009306
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| WBGene00009306 | SMap | S_parent | Sequence | F32A7 | |||||
|---|---|---|---|---|---|---|---|---|---|
| Identity | Version | 2 | |||||||
| Name | CGC_name | maph-1.1 | Person_evidence | WBPerson805 | |||||
| Sequence_name | F32A7.5 | ||||||||
| Molecular_name (12) | |||||||||
| Other_name | CELE_F32A7.5 | Accession_evidence | NDB | BX284601 | |||||
| Public_name | maph-1.1 | ||||||||
| DB_info | Database (11) | ||||||||
| Species | Caenorhabditis elegans | ||||||||
| History | Version_change | 1 | 26 May 2004 16:54:50 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of WS125 | ||
| 2 | 03 Jul 2015 12:05:46 | WBPerson2970 | Name_change | CGC_name | maph-1.1 | ||||
| Status | Live | ||||||||
| Gene_info | Biotype | SO:0001217 | |||||||
| Gene_class | maph | ||||||||
| Allele (77) | |||||||||
| RNASeq_FPKM (74) | |||||||||
| GO_annotation (23) | |||||||||
| Ortholog (48) | |||||||||
| Paralog | WBGene00007966 | Caenorhabditis elegans | From_analysis (3) | ||||||
| WBGene00009113 | Caenorhabditis elegans | From_analysis (2) | |||||||
| WBGene00018325 | Caenorhabditis elegans | From_analysis | modENCODE_Pseudogenes | ||||||
| Structured_description | Automated_description | Predicted to enable actin binding activity and microtubule binding activity. Predicted to be involved in microtubule cytoskeleton organization; neuron projection development; and regulation of microtubule depolymerization. Located in microtubule cytoskeleton. Expressed in body wall musculature; egg-laying apparatus; hypodermis; intestinal cell; and neurons. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness and periventricular nodular heterotopia. Is an ortholog of human MAP1A (microtubule associated protein 1A); MAP1B (microtubule associated protein 1B); and MAP1S (microtubule associated protein 1S). | 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:0050454 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6836) | ||||
| DOID:0050564 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6836) | ||||||
| Molecular_info | Corresponding_CDS | F32A7.5a | |||||||
| F32A7.5b | |||||||||
| F32A7.5c | |||||||||
| F32A7.5d | |||||||||
| Corresponding_transcript | F32A7.5a.1 | ||||||||
| F32A7.5b.1 | |||||||||
| F32A7.5c.1 | |||||||||
| F32A7.5d.1 | |||||||||
| Other_sequence | CJC09850_1 | ||||||||
| CRC06312_1 | |||||||||
| CR00627 | |||||||||
| CRC10472_1 | |||||||||
| CR01632 | |||||||||
| Associated_feature | WBsf657122 | ||||||||
| WBsf657123 | |||||||||
| WBsf717609 | |||||||||
| WBsf986244 | |||||||||
| WBsf1011301 | |||||||||
| WBsf218840 | |||||||||
| Experimental_info | RNAi_result (41) | ||||||||
| Expr_pattern | Expr13645 | ||||||||
| Expr1025913 | |||||||||
| Expr1034067 | |||||||||
| Expr1149977 | |||||||||
| Expr2013376 | |||||||||
| Expr2031608 | |||||||||
| Drives_construct | WBCnstr00032296 | ||||||||
| Construct_product | WBCnstr00032296 | ||||||||
| Microarray_results (30) | |||||||||
| Expression_cluster (175) | |||||||||
| Interaction (116) | |||||||||
| Map_info | Map | I | Position | 27.956 | |||||
| Positive | Positive_clone | F32A7 | Inferred_automatically | From sequence, transcript, pseudogene data | |||||
| Pseudo_map_position | |||||||||
| Reference (10) | |||||||||
| 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 |
