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WormBase Tree Display for Gene: WBGene00007591

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Name Class

WBGene00007591SMapS_parentSequenceC14H10
IdentityVersion2
NameCGC_namezipt-13Person_evidenceWBPerson341
Sequence_nameC14H10.1
Molecular_nameC14H10.1
C14H10.1.1
CE41296
Other_nameCELE_C14H10.1Accession_evidenceNDBBX284606
Public_namezipt-13
DB_infoDatabaseAceViewgeneXK854
WormQTLgeneWBGene00007591
WormFluxgeneWBGene00007591
NDBlocus_tagCELE_C14H10.1
PanthergeneCAEEL|WormBase=WBGene00007591|UniProtKB=Q17996
familyPTHR16950
NCBIgene181233
RefSeqproteinNM_077318.8
TrEMBLUniProtAccQ17996
UniProt_GCRPUniProtAccQ17996
OMIMgene608735
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
229 Nov 2016 11:06:21WBPerson2970Name_changeCGC_namezipt-13
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classzipt
Allele (80)
StrainWBStrain00037861
RNASeq_FPKM (74)
GO_annotation00059884
00059885
00059886
00059887
00059888
00115680
00115681
00115682
00115683
Ortholog (32)
ParalogWBGene00006487Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00006494Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
WBGene00044067Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to enable zinc ion transmembrane transporter activity. Predicted to be involved in intracellular zinc ion homeostasis and zinc ion transmembrane transport. Predicted to be located in membrane. Human ortholog(s) of this gene implicated in Ehlers-Danlos syndrome spondylodysplastic type 3. Is an ortholog of human SLC39A13 (solute carrier family 39 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
Disease_infoPotential_modelDOID:0080739Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20859)
DOID:13359Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:20859)
Molecular_infoCorresponding_CDSC14H10.1
Corresponding_CDS_historyC14H10.1:wp178
Corresponding_transcriptC14H10.1.1
Other_sequence (14)
Associated_featureWBsf654322
WBsf654323
WBsf1006659
WBsf1006660
WBsf1023691
WBsf237847
WBsf237848
WBsf237849
Experimental_infoRNAi_resultWBRNAi00010769Inferred_automaticallyRNAi_primary
WBRNAi00040568Inferred_automaticallyRNAi_primary
WBRNAi00000842Inferred_automaticallyRNAi_primary
Expr_patternExpr1014061
Expr1033271
Expr1144622
Expr2018165
Expr2036302
Drives_constructWBCnstr00033626
Construct_productWBCnstr00033626
Microarray_results (18)
Expression_cluster (162)
Interaction (11)
Map_infoMapXPosition1.90327
PositivePositive_cloneC14H10Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00038491
WBPaper00042629
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