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WormBase Tree Display for Gene: WBGene00022296

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Name Class

WBGene00022296SMapS_parentSequenceY76B12C
IdentityVersion2
NameCGC_namexpc-1Person_evidenceWBPerson2696
Sequence_nameY76B12C.2
Molecular_nameY76B12C.2
Y76B12C.2.1
CE31668
Other_nameCELE_Y76B12C.2Accession_evidenceNDBBX284604
Public_namexpc-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:31:05WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
219 May 2006 11:04:51WBPerson2970Name_changeCGC_namexpc-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classxpc
Allele (424)
StrainWBStrain00001746
WBStrain00001752
WBStrain00031598
WBStrain00007586
WBStrain00007587
WBStrain00007589
WBStrain00051050
RNASeq_FPKM (74)
GO_annotation (17)
Contained_in_operonCEOP4056
Ortholog (37)
Structured_descriptionAutomated_descriptionPredicted to enable damaged DNA binding activity and single-stranded DNA binding activity. Involved in response to UV. Predicted to be located in cytoplasm. Predicted to be part of XPC complex and nucleotide-excision repair factor 2 complex. Used to study xeroderma pigmentosum. Human ortholog(s) of this gene implicated in pancreatic cancer; serous cystadenocarcinoma; and xeroderma pigmentosum group C. Is an ortholog of human XPC (XPC complex subunit, DNA damage recognition and repair factor).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_infoExperimental_modelDOID:0050427Homo sapiensPaper_evidenceWBPaper00036260
Accession_evidenceOMIM278720
Curator_confirmedWBPerson324
Date_last_updated12 Dec 2013 00:00:00
Potential_modelDOID:0110844Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12816)
DOID:1793Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12816)
DOID:3114Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12816)
DOID:0050427Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:12816)
Models_disease_assertedWBDOannot00000255
Molecular_infoCorresponding_CDSY76B12C.2
Corresponding_CDS_historyY76B12C.2:wp82
Corresponding_transcriptY76B12C.2.1
Other_sequence (34)
Associated_featureWBsf034296
WBsf659960
WBsf995608
WBsf995609
WBsf227994
WBsf227995
Experimental_infoRNAi_resultWBRNAi00103083Inferred_automaticallyRNAi_primary
WBRNAi00103084Inferred_automaticallyRNAi_primary
WBRNAi00021476Inferred_automaticallyRNAi_primary
WBRNAi00103082Inferred_automaticallyRNAi_primary
WBRNAi00058496Inferred_automaticallyRNAi_primary
Expr_patternChronogram266
Expr7130
Expr14697
Expr1023363
Expr1039840
Expr1161905
Expr2018102
Expr2036240
Drives_constructWBCnstr00002561
WBCnstr00002567
Microarray_results (21)
Expression_cluster (128)
InteractionWBInteraction000037916
WBInteraction000040723
WBInteraction000043436
WBInteraction000043512
WBInteraction000520209
WBInteraction000539768
WBInteraction000549470
WBInteraction000551021
WBInteraction000575496
WBInteraction000582515
Map_infoMapIVPosition-12.3288Error0.148893
PositivePositive_cloneY76B12CInferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
Reference (18)
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