WormBase Tree Display for Gene: WBGene00019207
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WBGene00019207 | SMap | S_parent | Sequence | H17B01 | |||
---|---|---|---|---|---|---|---|
Identity | Version | 3 | |||||
Name | CGC_name | fdgt-1 | Person_evidence | WBPerson697 | |||
Sequence_name | H17B01.1 | ||||||
Molecular_name | H17B01.1a | ||||||
H17B01.1a.1 | |||||||
CE27184 | |||||||
H17B01.1b | |||||||
CE27185 | |||||||
H17B01.1b.1 | |||||||
Other_name | Y51H7BL.a | Curator_confirmed | WBPerson1983 | ||||
Remark | Old cosmid naming mapped via unique overlapping PCR_product on CDSs | ||||||
Y51H7BL.b | Curator_confirmed | WBPerson1983 | |||||
Remark | Old cosmid naming mapped via unique overlapping PCR_product on CDSs | ||||||
fgt-1 | Person_evidence | WBPerson697 | |||||
CELE_H17B01.1 | Accession_evidence | NDB | BX284602 | ||||
Public_name | fdgt-1 | ||||||
DB_info | Database | AceView | gene | 2B799 | |||
WormQTL | gene | WBGene00019207 | |||||
WormFlux | gene | WBGene00019207 | |||||
NDB | locus_tag | CELE_H17B01.1 | |||||
Panther | gene | CAEEL|WormBase=WBGene00019207|UniProtKB=O44827 | |||||
family | PTHR23503 | ||||||
NCBI | gene | 173525 | |||||
RefSeq | protein | NM_061580.7 | |||||
NM_061581.4 | |||||||
SwissProt | UniProtAcc | O44827 | |||||
UniProt_GCRP | UniProtAcc | O44827 | |||||
OMIM | gene | 138140 | |||||
138160 | |||||||
Species | Caenorhabditis elegans | ||||||
History | Version_change (3) | ||||||
Status | Live | ||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | fdgt | ||||||
Allele (135) | |||||||
Strain | WBStrain00054894 | ||||||
WBStrain00054929 | |||||||
RNASeq_FPKM (74) | |||||||
GO_annotation (12) | |||||||
Ortholog (58) | |||||||
Paralog (25) | |||||||
Structured_description | Automated_description | Predicted to enable hexose transmembrane transporter activity. Involved in glucose transmembrane transport. Predicted to be located in membrane. Expressed in hypodermis; intestinal cell; muscle cell; neurons; and pharynx. Human ortholog(s) of this gene implicated in several diseases, including Alzheimer's disease; Hirschsprung's disease; artery disease (multiple); and brain disease (multiple). Is an ortholog of human SLC2A14 (solute carrier family 2 member 14) and SLC2A3 (solute carrier family 2 member 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 (21) | ||||||
Molecular_info | Corresponding_CDS | H17B01.1a | |||||
H17B01.1b | |||||||
Corresponding_transcript | H17B01.1a.1 | ||||||
H17B01.1b.1 | |||||||
Other_sequence (87) | |||||||
Associated_feature | WBsf657341 | ||||||
WBsf657342 | |||||||
WBsf716971 | |||||||
WBsf986720 | |||||||
WBsf986721 | |||||||
WBsf986722 | |||||||
WBsf1011577 | |||||||
WBsf1011578 | |||||||
WBsf1011579 | |||||||
WBsf220848 | |||||||
Experimental_info | RNAi_result (11) | ||||||
Expr_pattern | Expr1684 | ||||||
Expr11125 | |||||||
Expr1020052 | |||||||
Expr1038294 | |||||||
Expr1153151 | |||||||
Expr2011755 | |||||||
Expr2029993 | |||||||
Drives_construct | WBCnstr00010374 | ||||||
WBCnstr00018173 | |||||||
Construct_product | WBCnstr00010374 | ||||||
WBCnstr00018173 | |||||||
Antibody | WBAntibody00002958 | ||||||
Microarray_results (32) | |||||||
Expression_cluster (155) | |||||||
Interaction (49) | |||||||
WBProcess | WBbiopr:00000121 | ||||||
Map_info | Map | II | Position | -15.4326 | Error | 0.001257 | |
Positive | Positive_clone | H17B01 | Inferred_automatically | From sequence, transcript, pseudogene data | |||
Pseudo_map_position | |||||||
Reference (14) | |||||||
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 |