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WormBase Tree Display for Gene: WBGene00016191

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Name Class

WBGene00016191SMapS_parentSequenceC28G1
IdentityVersion1
NameSequence_nameC28G1.6
Molecular_nameC28G1.6
C28G1.6.1
CE30885
Other_nameCELE_C28G1.6Accession_evidenceNDBBX284606
Public_nameC28G1.6
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
StatusLive
Gene_infoBiotypeSO:0001217
Allele (27)
StrainWBStrain00055379
RNASeq_FPKM (74)
GO_annotation00084528
00121873
Ortholog (204)
Paralog (22)
Structured_descriptionAutomated_descriptionPredicted to enable zinc ion binding activity. Human ortholog(s) of this gene implicated in several diseases, including Henoch-Schoenlein purpura; Sweet syndrome; and hematologic cancer (multiple). Is an ortholog of several human genes including MEFV (MEFV innate immunity regulator, pyrin); TRIM21 (tripartite motif containing 21); and TRIM27 (tripartite motif containing 27).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:4947Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:18064)
DOID:850Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
DOID:2987Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
DOID:9952Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
DOID:0050908Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
DOID:0080746Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
DOID:2841Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
DOID:11123Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
DOID:9538Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
DOID:9119Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6998)
Molecular_infoCorresponding_CDSC28G1.6
Corresponding_transcriptC28G1.6.1
Associated_featureWBsf654240
WBsf237726
Transcription_factorWBTranscriptionFactor000411
Experimental_infoRNAi_resultWBRNAi00041424Inferred_automaticallyRNAi_primary
Expr_patternExpr1012035
Expr1145454
Expr2001203
Expr2019425
Drives_constructWBCnstr00028257
Construct_productWBCnstr00028257
Microarray_results (12)
Expression_cluster (121)
Interaction (14)
Map_infoPositivePositive_cloneC28G1Inferred_automaticallyFrom sequence, transcript, pseudogene data
Interpolated_map_positionX0.417489
ReferenceWBPaper00027309
WBPaper00027315
WBPaper00038491
WBPaper00055090
MethodGene