WormBase Tree Display for Gene: WBGene00002192
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WBGene00002192 | SMap | S_parent | Sequence | CHROMOSOME_IV | |||
---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||
Name | CGC_name | kin-4 | |||||
Sequence_name | C10C6.1 | ||||||
Molecular_name (29) | |||||||
Other_name | CELE_C10C6.1 | Accession_evidence | NDB | BX284604 | |||
Public_name | kin-4 | ||||||
DB_info | Database (14) | ||||||
Species | Caenorhabditis elegans | ||||||
History | Version_change (2) | ||||||
Acquires_merge | WBGene00009040 | ||||||
Status | Live | ||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | kin | ||||||
Allele (245) | |||||||
Legacy_information | [C.elegansII] NMK. Encodes two protein kinase L isoforms, PKL1 (1528 aa, ST kinase, low in embryos, increases 5-fold on hatching) andPKL2 (1377 aa, different C-term, maximal in embryos, absent in L1). [CR] | ||||||
RNASeq_FPKM (74) | |||||||
GO_annotation (12) | |||||||
Ortholog (56) | |||||||
Paralog (15) | |||||||
Structured_description | Automated_description | Predicted to enable protein serine/threonine kinase activity. Predicted to be involved in intracellular signal transduction. Predicted to be located in cytoplasm. Expressed in head neurons; intestine; and tail neurons. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 108; female breast cancer; and mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations. Is an ortholog of human MAST1 (microtubule associated serine/threonine kinase 1) and MAST3 (microtubule associated serine/threonine kinase 3). | 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:0111403 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:19034) | ||
DOID:0070394 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:19036) | ||||
DOID:0050671 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:19034) | ||||
Molecular_info | Corresponding_CDS | C10C6.1a | |||||
C10C6.1b | |||||||
C10C6.1c | |||||||
C10C6.1d | |||||||
C10C6.1e | |||||||
C10C6.1f | |||||||
C10C6.1g | |||||||
C10C6.1h | |||||||
C10C6.1i | |||||||
Corresponding_CDS_history | C10C6.1:wp149 | ||||||
Corresponding_transcript (11) | |||||||
Other_sequence (45) | |||||||
Associated_feature (23) | |||||||
Experimental_info | RNAi_result | WBRNAi00113413 | Inferred_automatically | RNAi_primary | |||
WBRNAi00113414 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00000907 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00040289 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00113415 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00064529 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00010589 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00002004 | Inferred_automatically | RNAi_primary | |||||
Expr_pattern | Expr14620 | ||||||
Expr14621 | |||||||
Expr14622 | |||||||
Expr14623 | |||||||
Expr1015031 | |||||||
Expr1031285 | |||||||
Expr1144362 | |||||||
Expr2012943 | |||||||
Expr2031175 | |||||||
Drives_construct | WBCnstr00036398 | ||||||
WBCnstr00041179 | |||||||
WBCnstr00041180 | |||||||
WBCnstr00041181 | |||||||
Construct_product | WBCnstr00036398 | ||||||
WBCnstr00041179 | |||||||
WBCnstr00041180 | |||||||
Microarray_results (33) | |||||||
Expression_cluster (159) | |||||||
Interaction (100) | |||||||
Map_info | Map | IV | Position | 4.98015 | Error | 0.00152 | |
Positive | Positive_clone | C10C6 | Inferred_automatically | From sequence, transcript, pseudogene data | |||
CR#KIN4 | |||||||
Mapping_data | Multi_point | 5044 | |||||
Pseudo_map_position | |||||||
Reference (16) | |||||||
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 |