WormBase Tree Display for Gene: WBGene00012967
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WBGene00012967 | SMap | S_parent | Sequence | Y48A6B | |||
---|---|---|---|---|---|---|---|
Identity (6) | |||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | kvs | ||||||
Allele (189) | |||||||
Strain | WBStrain00055287 | ||||||
RNASeq_FPKM (74) | |||||||
GO_annotation (27) | |||||||
Contained_in_operon | CEOP3712 | ||||||
Ortholog (54) | |||||||
Paralog (13) | |||||||
Structured_description | Automated_description | Predicted to enable delayed rectifier potassium channel activity. Predicted to be involved in potassium ion transmembrane transport. Predicted to be located in axon; plasma membrane; and somatodendritic compartment. Predicted to be part of voltage-gated potassium channel complex. Expressed in AVA and nervous system. Human ortholog(s) of this gene implicated in developmental and epileptic encephalopathy 26. Is an ortholog of human KCNF1 (potassium voltage-gated channel modifier subfamily F member 1) and KCNS2 (potassium voltage-gated channel modifier subfamily S member 2). | 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:0080461 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6231) | ||
DOID:1826 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:6231) | ||||
Molecular_info (5) | |||||||
Experimental_info | RNAi_result | WBRNAi00006209 | Inferred_automatically | RNAi_primary | |||
WBRNAi00037221 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00006717 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00056866 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00020727 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00056865 | Inferred_automatically | RNAi_primary | |||||
Expr_pattern | Expr12745 | ||||||
Expr12746 | |||||||
Expr15545 | |||||||
Expr1024741 | |||||||
Expr1160318 | |||||||
Expr2012987 | |||||||
Expr2031219 | |||||||
Drives_construct | WBCnstr00022466 | ||||||
Construct_product | WBCnstr00022463 | ||||||
WBCnstr00022727 | |||||||
Microarray_results (24) | |||||||
Expression_cluster (104) | |||||||
Interaction (17) | |||||||
Map_info | Map | III | Position | 5.85665 | Error | 0.005556 | |
Positive | Positive_clone | Y48A6B | Inferred_automatically | From sequence, transcript, pseudogene data | |||
Pseudo_map_position | |||||||
Reference | WBPaper00027009 | ||||||
WBPaper00038491 | |||||||
WBPaper00049107 | |||||||
WBPaper00055090 | |||||||
WBPaper00062255 | |||||||
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 |