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WormBase Tree Display for Gene: WBGene00019207

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Name Class

WBGene00019207SMapS_parentSequenceH17B01
Identity (6)
Gene_infoBiotypeSO:0001217
Gene_classfdgt
Allele (135)
StrainWBStrain00054894
WBStrain00054929
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (58)
Paralog (25)
Structured_descriptionAutomated_descriptionPredicted 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_evidenceWBPaper00065943
Curator_confirmedWBPerson324
WBPerson37462
Inferred_automaticallyThis description was generated automatically by a script based on data from the WS291 version of WormBase
Date_last_updated29 Nov 2023 00:00:00
Disease_infoPotential_model (21)
Molecular_infoCorresponding_CDSH17B01.1a
H17B01.1b
Corresponding_transcriptH17B01.1a.1
H17B01.1b.1
Other_sequence (87)
Associated_featureWBsf657341
WBsf657342
WBsf716971
WBsf986720
WBsf986721
WBsf986722
WBsf1011577
WBsf1011578
WBsf1011579
WBsf220848
Experimental_infoRNAi_result (11)
Expr_patternExpr1684
Expr11125
Expr1020052
Expr1038294
Expr1153151
Expr2011755
Expr2029993
Drives_constructWBCnstr00010374
WBCnstr00018173
Construct_productWBCnstr00010374
WBCnstr00018173
AntibodyWBAntibody00002958
Microarray_results (32)
Expression_cluster (155)
Interaction (49)
WBProcessWBbiopr:00000121
Map_infoMapIIPosition-15.4326Error0.001257
PositivePositive_cloneH17B01Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (14)
RemarkMap 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
MethodGene