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WormBase Tree Display for Gene: WBGene00014092

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Name Class

WBGene00014092SMapS_parentSequenceZK822
IdentityVersion2
NameCGC_nameslc-5A12Author_evidenceWBPerson555
Sequence_nameZK822.5
Molecular_nameZK822.5
ZK822.5.1
CE18466
Other_nameCELE_ZK822.5Accession_evidenceNDBBX284604
Public_nameslc-5A12
DB_infoDatabaseAceViewgene4M703
WormQTLgeneWBGene00014092
WormFluxgeneWBGene00014092
NDBlocus_tagCELE_ZK822.5
PanthergeneCAEEL|WormBase=WBGene00014092|UniProtKB=Q23616
familyPTHR42985
NCBIgene178127
RefSeqproteinNM_001047602.6
TrEMBLUniProtAccQ23616
UniProt_GCRPUniProtAccQ23616
OMIMgene601843
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:55WBPerson1971EventImportedInitial conversion from CDS class of WS125
210 Jul 2023 23:47:10WBPerson51134Name_changeCGC_nameslc-5A12
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classslc
Allele (41)
StrainWBStrain00001221
WBStrain00032464
RNASeq_FPKM (74)
GO_annotation00057527
00057528
00057529
00057530
00057531
00057532
00120820
00120821
00120822
Ortholog (65)
ParalogWBGene00018716Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00000501Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable symporter activity. Predicted to be involved in sodium ion transport. Predicted to be located in membrane. Expressed in several structures, including intestine; nervous system; non-striated muscle; pharynx; and rectal gland cell. Human ortholog(s) of this gene implicated in thyroid dyshormonogenesis 1. Is an ortholog of human SLC5A12 (solute carrier family 5 member 12) and SLC5A8 (solute carrier family 5 member 8).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:0112185Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11040)
DOID:0050328Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:11040)
Molecular_infoCorresponding_CDSZK822.5
Corresponding_CDS_historyZK822.5b:wp288
Corresponding_transcriptZK822.5.1
Other_sequence (23)
Associated_featureWBsf646436
WBsf660772
WBsf997993
WBsf229223
Experimental_infoRNAi_resultWBRNAi00081182Inferred_automaticallyRNAi_primary
WBRNAi00022181Inferred_automaticallyRNAi_primary
WBRNAi00059746Inferred_automaticallyRNAi_primary
WBRNAi00038452Inferred_automaticallyRNAi_primary
WBRNAi00059745Inferred_automaticallyRNAi_primary
Expr_patternChronogram1396
Expr7257
Expr7258
Expr1019115
Expr1036312
Expr1163169
Expr2008982
Expr2027218
Drives_constructWBCnstr00002114
WBCnstr00004223
WBCnstr00029316
Construct_productWBCnstr00029316
Microarray_results (27)
Expression_cluster (150)
Interaction (15)
Map_infoMapIVPosition5.43389
PositivePositive_cloneZK822Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00034662
WBPaper00038491
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