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WormBase Tree Display for Gene: WBGene00010811

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Name Class

WBGene00010811SMapS_parentSequenceM01F1
IdentityVersion2
NameCGC_namehmit-1.3Person_evidenceWBPerson353
Sequence_nameM01F1.5
Molecular_nameM01F1.5
M01F1.5.1
CE33672
M01F1.5.2
Other_nameCELE_M01F1.5Accession_evidenceNDBBX284603
Public_namehmit-1.3
DB_infoDatabaseAceViewgene3E602
WormQTLgeneWBGene00010811
WormFluxgeneWBGene00010811
NDBlocus_tagCELE_M01F1.5
PanthergeneCAEEL|WormBase=WBGene00010811|UniProtKB=Q21455
familyPTHR48020
NCBIgene175458
RefSeqproteinNM_065324.7
SwissProtUniProtAccQ21455
TREEFAMTREEFAM_IDTF314916
UniProt_GCRPUniProtAccQ21455
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
216 Feb 2007 14:39:36WBPerson2970Name_changeCGC_namehmit-1.3
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhmit
Allele (150)
StrainWBStrain00001545
RNASeq_FPKM (74)
GO_annotation (12)
Ortholog (31)
Paralog (25)
Structured_descriptionConcise_descriptionhmit-1.3 encodes one of three C. elegans proton (H+)-dependent myo-inositol transporters; loss of hmit-1.3 activity via large-scale RNAi result in no obvious abnormalities but by homology, HMIT-1.3 is predicted to function as a plasma membrane protein required for the regulated uptake of myo-inositol and thus potentially for regulation of cell signaling and intracellular osmolarity.Curator_confirmedWBPerson1843
Date_last_updated25 Apr 2007 00:00:00
Automated_descriptionPredicted to enable myo-inositol:proton symporter activity. Predicted to be involved in myo-inositol transport and transmembrane transport. Located in apical plasma membrane. Expressed in amphid sheath cell; head; and phasmid sheath cell. Is an ortholog of human SLC2A13 (solute carrier family 2 member 13).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
Molecular_infoCorresponding_CDSM01F1.5
Corresponding_CDS_historyM01F1.5:wp98
Corresponding_transcriptM01F1.5.1
M01F1.5.2
Other_sequence (66)
Associated_featureWBsf650911
WBsf666424
WBsf666650
WBsf716728
WBsf991795
WBsf1014577
WBsf226358
Experimental_infoRNAi_resultWBRNAi00006197Inferred_automaticallyRNAi_primary
WBRNAi00034362Inferred_automaticallyRNAi_primary
WBRNAi00050771Inferred_automaticallyRNAi_primary
WBRNAi00017104Inferred_automaticallyRNAi_primary
Expr_patternChronogram559
Expr6405
Expr9310
Expr9313
Expr1012926
Expr1034738
Expr1154466
Expr2012528
Expr2030767
Drives_constructWBCnstr00002387
WBCnstr00008841
WBCnstr00013891
WBCnstr00013894
Construct_productWBCnstr00013894
Microarray_results (19)
Expression_cluster (167)
Interaction (58)
Map_infoMapIIIPosition-6.13586Error0.06541
PositivePositive_cloneM01F1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00038529
WBPaper00055090
WBPaper00065331
WBPaper00065341
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