WormBase Tree Display for Gene: WBGene00019207
expand all nodes | collapse all nodes | view schema
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 | 1 | 28 May 2004 13:31:01 | WBPerson1971 | Event | Imported | Initial conversion from CDS class of stlace from WS125 | ||
2 | 14 Oct 2011 15:24:19 | WBPerson2970 | Name_change | CGC_name | fgt-1 | ||||
3 | 12 Jan 2023 20:48:33 | WBPerson51134 | Name_change | CGC_name | fdgt-1 | ||||
Other_name | fgt-1 | ||||||||
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 |