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WormBase Tree Display for Gene: WBGene00016539

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Name Class

WBGene00016539SMapS_parentSequenceC39F7
IdentityVersion6
NameCGC_namemadd-2Person_evidenceWBPerson1820
Sequence_nameC39F7.2
Molecular_nameC39F7.2a
C39F7.2a.1
CE27581
C39F7.2b
CE42345
C39F7.2c
CE51042
C39F7.2b.1
C39F7.2c.1
Other_namerax-1Person_evidenceWBPerson160
trim-9Person_evidenceWBPerson232
WBPerson11460
WBPerson274
Y50D4A.aCurator_confirmedWBPerson1983
RemarkOld cosmid naming mapped via unique overlapping PCR_product on CDSs
CELE_C39F7.2Accession_evidenceNDBBX284605
Public_namemadd-2
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
230 Mar 2009 16:33:08WBPerson9133Name_changeCGC_nametrim-9
330 Apr 2010 11:15:49WBPerson2970Name_changeCGC_namemadd-2
Other_nametrim-9
403 Mar 2011 09:42:53WBPerson2970Name_changeCGC_nametrim-9
Other_namemadd-2
524 Mar 2011 10:05:31WBPerson2970EventAcquires_mergeWBGene00044993
Name_changeOther_namerax-1
628 Apr 2014 11:30:35WBPerson2970Name_changeCGC_namemadd-2
Other_nametrim-9
Acquires_mergeWBGene00044993
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmadd
AlleleWBVar00278526
WBVar00296537
WBVar00000606
WBVar02031743
WBVar00580898
WBVar02031744
WBVar00580901
WBVar00580902
WBVar00580904
WBVar00580905
WBVar00580907
WBVar00580908
WBVar01488665
WBVar00580909
WBVar02023014
WBVar01584508
WBVar01584509
WBVar01584510
WBVar01499528
WBVar01584511
WBVar01584512
WBVar01584513
WBVar01584514
WBVar01499167
WBVar01490522
WBVar02147291
WBVar00984937
WBVar00984938
WBVar00984939
WBVar00984940
WBVar00984941
WBVar00984942
WBVar00984943
WBVar00984944
WBVar01774726
WBVar00984945
WBVar00984946
WBVar01499740
WBVar01774727
WBVar00984947
WBVar01774728
WBVar00984948
WBVar01774729
WBVar01774730
WBVar00984949
WBVar01774731
WBVar00984950
WBVar01774732
WBVar00984951
WBVar01774733
WBVar00984952
WBVar01774734
WBVar00984953
WBVar01774735
WBVar00984954
WBVar00984955
WBVar01774736
WBVar01774737
WBVar02145245
WBVar00984956
WBVar00984957
WBVar00984958
WBVar00984959
WBVar00984960
WBVar00984961
WBVar00984962
WBVar00984963
WBVar00984964
WBVar00984965
WBVar00984966
WBVar00984967
WBVar00984968
WBVar00984969
WBVar00984970
WBVar00984971
WBVar00598824
WBVar00984972
WBVar00984973
WBVar01985358
WBVar00984974
WBVar01985359
WBVar00984975
WBVar01985360
WBVar00984976
WBVar00265239
WBVar00984977
WBVar00984978
WBVar00984979
WBVar01848329
WBVar00984980
WBVar00984981
WBVar00984982
WBVar01661151
WBVar00984983
WBVar01457965
WBVar01457966
WBVar00984984
WBVar01457967
WBVar00984985
WBVar01457968
WBVar00984986
WBVar00984987
WBVar01457970
WBVar00984988
WBVar01457972
WBVar01457973
WBVar00984989
WBVar00984990
WBVar01499784
WBVar00260101
WBVar01457974
WBVar00984991
WBVar01457975
WBVar01457976
WBVar00984992
WBVar01457977
WBVar00984993
WBVar00984994
WBVar00984995
WBVar00984996
WBVar00984997
WBVar00984998
WBVar01521383
WBVar00984999
WBVar01521384
WBVar00985000
WBVar01521385
WBVar00985001
WBVar01521386
WBVar00449547
WBVar01970867
WBVar01521387
WBVar00985002
WBVar00449548
WBVar00985003
WBVar01970868
WBVar01521388
WBVar00449549
WBVar00449550
WBVar01521389
WBVar01970869
WBVar00985004
WBVar00985005
WBVar00449551
WBVar01970870
WBVar00985006
WBVar01970871
WBVar02008804
WBVar00449552
WBVar00449553
WBVar01970872
WBVar00985007
WBVar01970873
WBVar00449554
WBVar00985008
WBVar00449555
WBVar01970874
WBVar00985009
WBVar00449556
WBVar00985010
WBVar01970875
WBVar00985011
WBVar00449557
WBVar00449558
WBVar00985012
WBVar00449559
WBVar00985013
WBVar00449560
WBVar00256629
WBVar00985014
WBVar00449561
WBVar00985015
WBVar00278513
WBVar00449562
WBVar00278514
WBVar00256631
WBVar00985016
WBVar00449563
WBVar00278515
WBVar00985017
WBVar00278516
WBVar00449564
WBVar00985018
WBVar00985019
WBVar00278517
WBVar00449565
WBVar00985020
WBVar00449566
WBVar00278518
WBVar00278519
WBVar00449567
WBVar00985021
WBVar00449568
WBVar00278520
WBVar00985022
WBVar00449569
WBVar00985023
WBVar00278521
WBVar00985024
WBVar00278522
WBVar00449570
WBVar00449571
WBVar00278523
WBVar00985025
WBVar00449572
WBVar01737635
WBVar00278524
WBVar00278525
WBVar00449573
WBVar00449574
WBVar00449575
WBVar01924640
WBVar00449576
WBVar01924641
WBVar00449577
WBVar02051822
WBVar00449578
WBVar00449579
WBVar02051823
WBVar02051824
WBVar00449580
WBVar00449581
WBVar02051825
WBVar00449582
WBVar02051826
WBVar00449583
WBVar00000610
WBVar00449584
WBVar00449585
WBVar00202601
WBVar00449586
WBVar00202602
WBVar00449587
WBVar00202603
WBVar00449588
WBVar00202604
WBVar00449589
WBVar00449590
WBVar00202605
WBVar00202606
WBVar00449591
WBVar02135684
WBVar00202607
WBVar00449592
WBVar02135685
WBVar00449593
WBVar00202608
WBVar00202609
WBVar02135686
WBVar00316761
WBVar00316762
WBVar01483472
WBVar00260174
WBVar00093390
WBVar01499496
WBVar01833775
WBVar01833776
WBVar01833777
WBVar01833778
WBVar01833779
WBVar01833780
WBVar01833781
WBVar01674162
WBVar02031740
WBVar02031741
WBVar01500066
WBVar02031742
WBVar00580897
StrainWBStrain00032432
WBStrain00033425
WBStrain00033426
WBStrain00007190
RNASeq_FPKM (74)
GO_annotation (26)
Ortholog (58)
Paralog (19)
Structured_descriptionConcise_descriptionmadd-2 encodes a protein containing RBCC/TRIM, fibronectin type III, and SPRY domains that is the sole C. elegans member of the C1 subfamily of tripartite motif (TRIM) proteins and is homologous to mammalian TRIM9, TRIM67, and MID1/TRIM18, mutations in which result in Opitz G/BBB syndrome, a congenital malformation disorder affecting ventral midline structures and resulting in mental retardation; in C. elegans, MADD-2 functions cell autonomously as a specificity factor in an UNC-6/Netrin, and UNC-40/DCC-mediated pathway that regulates axon branch formation and attractive axon guidance in multiple neuronal types by potentiating UNC-40 activity; in addition, MADD-2 is required for ventral recruitment of MIG-10/Lamellopodin in the HSNs during outgrowth; MADD-2 also functions cell autonomously in body wall muscle in an UNC-40/DCC and UNC-73/Rho-GEF-mediated pathway to regulate muscle arm extension to ventral midline motor axons; MADD-2 exhibits E3 ubiquitin ligase activity in vitro, physically interacts with both UNC-40 and UNC-73, and may potentiate the in vivo interaction between UNC-40 and UNC-73; a MADD-2::GFP fusion protein is expressed in neurons, hypodermis, and muscle cells; expression is also seen in the anchor cell, the ventral uterine precursor cells and in the ray precursors and descendants in males; in neurons, MADD-2 colocalizes with UNC-40 to the ventral axon branches that require its function; in body wall muscle, MADD-2 localizes to the dense bodies and colocalizes to the muscle arm termini with UNC-40 and UNC-73.Paper_evidenceWBPaper00032907
WBPaper00036484
WBPaper00036485
WBPaper00038152
Curator_confirmedWBPerson1843
Date_last_updated02 Apr 2014 00:00:00
Automated_descriptionEnables protein homodimerization activity; signaling receptor binding activity; and ubiquitin-protein transferase activity. Involved in cell projection organization; protein ubiquitination; and regulation of protein localization. Located in several cellular components, including cell leading edge; neuronal cell body; and striated muscle dense body. Expressed in several structures, including anchor cell; intestinal cell; muscle cell; neurons; and ray precursor cell. Used to study Opitz GBBB syndrome. Human ortholog(s) of this gene implicated in Opitz GBBB syndrome; anencephaly; and non-syndromic X-linked intellectual disability 101. Is an ortholog of human TRIM67 (tripartite motif containing 67) and TRIM9 (tripartite motif containing 9).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:0080697Homo sapiensPaper_evidenceWBPaper00036485
Curator_confirmedWBPerson324
Date_last_updated16 Feb 2021 00:00:00
Potential_modelDOID:0060668Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:16280)
DOID:0112048Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7096)
DOID:0080697Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:7095)
Models_disease_assertedWBDOannot00000855
WBDOannot00000856
WBDOannot00000857
Molecular_infoCorresponding_CDSC39F7.2a
C39F7.2b
C39F7.2c
Corresponding_CDS_historyC39F7.2:wp188
Corresponding_transcriptC39F7.2a.1
C39F7.2b.1
C39F7.2c.1
Other_sequence (20)
Associated_feature (21)
Experimental_infoRNAi_resultWBRNAi00011797Inferred_automaticallyRNAi_primary
WBRNAi00065292Inferred_automaticallyRNAi_primary
WBRNAi00076206Inferred_automaticallyRNAi_primary
WBRNAi00042229Inferred_automaticallyRNAi_primary
WBRNAi00011796Inferred_automaticallyRNAi_primary
WBRNAi00020824Inferred_automaticallyRNAi_primary
WBRNAi00080808Inferred_automaticallyRNAi_primary
Expr_pattern (15)
Drives_constructWBCnstr00002505
WBCnstr00007149
WBCnstr00007634
WBCnstr00017575
Construct_product (13)
Microarray_results (26)
Expression_cluster (158)
Interaction (28)
Anatomy_functionWBbtf0412
WBbtf0413
WBbtf0598
Map_infoMapVPosition-19.8476Error0.000552
PositivePositive_cloneC39F7Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataPos_neg_data10757
Pseudo_map_position
Reference (15)
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