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 | TreeFam | |||||
Inparanoid_8 | |||||||||
WormBase-Compara | |||||||||
WBGene00009113 | Caenorhabditis elegans | From_analysis | Inparanoid_8 | ||||||
WormBase-Compara | |||||||||
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 (6) | |||||||||
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 (3) | |||||||||
Reference | WBPaper00029395 | ||||||||
WBPaper00038491 | |||||||||
WBPaper00049959 | |||||||||
WBPaper00055090 | |||||||||
WBPaper00059214 | |||||||||
WBPaper00059548 | |||||||||
WBPaper00060754 | |||||||||
WBPaper00062248 | |||||||||
WBPaper00064789 | |||||||||
WBPaper00065165 | |||||||||
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 |