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WormBase Tree Display for Gene: WBGene00013073

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Name Class

WBGene00013073SMapS_parentSequenceY51A2D
IdentityVersion2
NameCGC_namehmit-1.1Person_evidenceWBPerson353
Sequence_nameY51A2D.4
Molecular_nameY51A2D.4
Y51A2D.4.1
CE19201
Other_nameCELE_Y51A2D.4Accession_evidenceNDBBX284605
Public_namehmit-1.1
DB_infoDatabaseAceViewgene5T3
WormQTLgeneWBGene00013073
WormFluxgeneWBGene00013073
NDBlocus_tagCELE_Y51A2D.4
PanthergeneCAEEL|WormBase=WBGene00013073|UniProtKB=Q9XXR3
familyPTHR48020
NCBIgene180205
RefSeqproteinNM_075222.5
SwissProtUniProtAccQ9XXR3
TREEFAMTREEFAM_IDTF314916
UniProt_GCRPUniProtAccQ9XXR3
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:54WBPerson1971EventImportedInitial conversion from CDS class of WS125
216 Feb 2007 14:39:36WBPerson2970Name_changeCGC_namehmit-1.1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classhmit
Allele (254)
StrainWBStrain00032845
RNASeq_FPKM (74)
GO_annotation (11)
Ortholog (40)
Paralog (25)
Structured_descriptionConcise_descriptionhmit-1.1 encodes one of three C. elegans proton (H+)-dependent myo-inositol transporters; loss of hmit-1.1 activity via large-scale RNAi result in no obvious abnormalities but by homology, HMIT-1.1 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 intestinal 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_CDSY51A2D.4
Corresponding_transcriptY51A2D.4.1
Other_sequence (21)
Associated_featureWBsf647682
WBsf1002922
WBsf1002923
WBsf1002924
Experimental_infoRNAi_resultWBRNAi00057137Inferred_automaticallyRNAi_primary
WBRNAi00097120Inferred_automaticallyRNAi_primary
WBRNAi00020873Inferred_automaticallyRNAi_primary
WBRNAi00037349Inferred_automaticallyRNAi_primary
Expr_patternExpr9308
Expr9311
Expr1016622
Expr1035802
Expr1160584
Expr2012526
Expr2030765
Drives_constructWBCnstr00008839
WBCnstr00008842
WBCnstr00008844
WBCnstr00013889
WBCnstr00013892
Construct_productWBCnstr00008842
WBCnstr00013892
Microarray_results (19)
Expression_cluster (318)
Interaction (41)
Map_infoMapVPosition16.8086Error0.020702
PositivePositive_cloneY51A2DInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00036738
WBPaper00038491
WBPaper00038529
WBPaper00055090
WBPaper00060410
WBPaper00064375
WBPaper00064435
WBPaper00065156
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