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WormBase Tree Display for Gene: WBGene00010867

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Name Class

WBGene00010867SMapS_parentSequenceM04G12
IdentityVersion3
NameCGC_nameifbp-1
Sequence_nameM04G12.1
Molecular_name (30)
Other_nametag-260
CELE_M04G12.1Accession_evidenceNDBBX284605
Public_nameifbp-1
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:51WBPerson1971EventImportedInitial conversion from CDS class of WS125
222 Apr 2005 11:55:18WBPerson2970Name_changeCGC_nametag-260
310 Sep 2020 13:47:56WBPerson1983Name_changeCGC_nameifbp-1
Other_nametag-260
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classifbp
Allele (166)
StrainWBStrain00031982
WBStrain00036086
RNASeq_FPKM (74)
GO_annotation00003496
00003497
00051747
00051748
00051749
00051750
00051751
00051752
00051753
00051754
Ortholog (43)
ParalogWBGene00009939Caenorhabditis elegansFrom_analysisWormBase-Compara
Structured_descriptionAutomated_descriptionPredicted to be located in nucleus. Human ortholog(s) of this gene implicated in common variable immunodeficiency 14 and neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures. Is an ortholog of human IRF2BP2 (interferon regulatory factor 2 binding protein 2) and IRF2BPL (interferon regulatory factor 2 binding protein like).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:0081327Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:14282)
DOID:0081156Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:21729)
Molecular_infoCorresponding_CDSM04G12.1a
M04G12.1b
M04G12.1c
M04G12.1d
M04G12.1e
M04G12.1f
M04G12.1g
M04G12.1h
M04G12.1i
M04G12.1j
Corresponding_CDS_historyM04G12.1a:wp90
Corresponding_transcript (10)
Other_sequenceCR07359
SS00835
Oden_isotig12801
JI460334.1
FG347839.1
HGC04002_1
HCC07234_1
FG348012.1
MIC04144_1
EX538912.1
HG08756
BMC17207_1
HC05525
ACC06251_1
JI165734.1
MIC06126_1
FG582668.1
TS00326
Dviv_isotig16045
FG353846.1
BUC02069_1
FD514548.1
FG354105.1
Oden_isotig12803
SSC00470_1
FG350686.1
EX543405.1
SRC00622_1
FG350721.1
FC815099.1
JI484046.1
CSC01677_1
Tcir_isotig19816
JI483126.1
JI473548.1
MI05582
TSC00239_1
ES567960.1
MI00300
Acan_isotig09662
FK803357.1
GO239586.1
FG586013.1
JI216442.1
CRC00389_1
FG588016.1
EY472641.1
Dviv_isotig16044
FK801577.1
AS12058
ASC04161_1
Associated_feature (25)
Experimental_infoRNAi_resultWBRNAi00050916Inferred_automaticallyRNAi_primary
WBRNAi00034431Inferred_automaticallyRNAi_primary
WBRNAi00046174Inferred_automaticallyRNAi_primary
WBRNAi00017183Inferred_automaticallyRNAi_primary
WBRNAi00073227Inferred_automaticallyRNAi_primary
WBRNAi00076576Inferred_automaticallyRNAi_primary
Expr_patternExpr1018818
Expr1034761
Expr1154614
Expr2017250
Expr2035386
Drives_constructWBCnstr00031098
Construct_productWBCnstr00031098
Microarray_results (36)
Expression_cluster (151)
Interaction (148)
Map_infoMapVPosition5.20783Error0.004132
PositivePositive_cloneM04G12Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point5214
4908
5548
Pseudo_map_position
ReferenceWBPaper00029058
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