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WormBase Tree Display for Gene: WBGene00015676

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Name Class

WBGene00015676SMapS_parentSequenceC10E2
IdentityVersion2
NameCGC_namemct-6Paper_evidenceWBPaper00041876
Person_evidenceWBPerson3620
Sequence_nameC10E2.6
Molecular_nameC10E2.6
C10E2.6.1
CE29573
Other_nameCELE_C10E2.6Accession_evidenceNDBBX284606
Public_namemct-6
DB_infoDatabaseAceViewgeneXR382
WormQTLgeneWBGene00015676
WormFluxgeneWBGene00015676
NDBlocus_tagCELE_C10E2.6
PanthergeneCAEEL|WormBase=WBGene00015676|UniProtKB=O17328
familyPTHR11360
NCBIgene181724
RefSeqproteinNM_078304.8
TrEMBLUniProtAccO17328
UniProt_GCRPUniProtAccO17328
OMIMgene600682
611910
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:56WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
209 Jan 2013 14:59:12WBPerson2970Name_changeCGC_namemct-6
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmct
Allele (61)
StrainWBStrain00002867
RNASeq_FPKM (74)
GO_annotation00029632
00029633
00029634
00029635
00121480
00121481
Ortholog (72)
ParalogWBGene00003986Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00008214Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010340Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00010834Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00013353Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00015273Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00020168Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00017369Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00021227Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable monocarboxylic acid transmembrane transporter activity. Predicted to be involved in monocarboxylic acid transport. Predicted to be located in membrane. Expressed in tail. Human ortholog(s) of this gene implicated in cataract 47; familial hyperinsulinemic hypoglycemia 7; and lymphangioleiomyomatosis. Is an ortholog of several human genes including SLC16A1 (solute carrier family 16 member 1); SLC16A6 (solute carrier family 16 member 6); and SLC16A7 (solute carrier family 16 member 7).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_modelDOID:3319Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10922)
DOID:0070353Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:23094)
DOID:0070214Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:10922)
Molecular_infoCorresponding_CDSC10E2.6
Corresponding_transcriptC10E2.6.1
Other_sequence (46)
Associated_feature (14)
Experimental_infoRNAi_result (14)
Expr_patternChronogram1735
Expr5232
Expr1022754
Expr1036708
Expr1144373
Expr2013460
Expr2031694
Drives_constructWBCnstr00003387
WBCnstr00028663
Construct_productWBCnstr00028663
Microarray_results (20)
Expression_cluster (164)
Interaction (24)
Map_infoMapXPosition24.0604
PositivePositive_cloneC10E2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00055090
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