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WormBase Tree Display for Gene: WBGene00003509

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Name Class

WBGene00003509SMapS_parentSequenceT19B10
IdentityVersion1
NameCGC_namemxl-1
Sequence_nameT19B10.11
Molecular_nameT19B10.11
T19B10.11.1
CE16417
Other_nameCELE_T19B10.11Accession_evidenceNDBBX284605
Public_namemxl-1
DB_infoDatabaseAceViewgene5L725
WormQTLgeneWBGene00003509
WormFluxgeneWBGene00003509
NDBlocus_tagCELE_T19B10.11
PanthergeneCAEEL|WormBase=WBGene00003509|UniProtKB=G5EEH5
familyPTHR10328
NCBIgene179557
RefSeqproteinNM_073455.7
SwissProtUniProtAccG5EEH5
UniProt_GCRPUniProtAccG5EEH5
OMIMgene154950
SpeciesCaenorhabditis elegans
HistoryVersion_change107 Apr 2004 11:29:32WBPerson1971EventImportedInitial conversion from geneace
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmxl
Allele (17)
Legacy_information[Yuan J, Cole MD] No mutations known. Related to vertebrate MAX transcription factor, MXL-1 can form DNA-binding heterodimer with MDL-1 in vitro. mxl-1::GFP expression strongest in intestinal cells. Predicted gene T19B10.11.
RNASeq_FPKM (74)
GO_annotation (18)
Contained_in_operonCEOP5280
Ortholog (28)
ParalogWBGene00003511Caenorhabditis elegansFrom_analysisPanther
WormBase-Compara
Structured_descriptionConcise_descriptionmxl-1 encodes a basic helix-loop-helix protein similar to the vertebrate MAX transcriptional regulators; in vitro, MXL-1 can heterodimerize, and bind an E-box DNA sequence, with MDL-1, a C. elegans MAD-like bHLH protein; mxl-1::gfp reporter fusions are expressed in the posterior intestine and in head and tail neurons.Paper_evidenceWBPaper00003190
Curator_confirmedWBPerson1843
Date_last_updated11 Sep 2007 00:00:00
Automated_descriptionEnables protein domain specific binding activity and protein heterodimerization activity. Contributes to sequence-specific DNA binding activity. Involved in determination of adult lifespan. Located in nucleus. Part of transcription regulator complex. Expressed in tail neurons. Human ortholog(s) of this gene implicated in lung small cell carcinoma and pheochromocytoma. Is an ortholog of human MAX (MYC associated factor X).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:5409Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6913)
DOID:0050771Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:6913)
Molecular_infoCorresponding_CDST19B10.11
Corresponding_transcriptT19B10.11.1
Other_sequence (22)
Associated_featureWBsf647243
WBsf978665
WBsf232485
WBsf232486
Transcription_factorWBTranscriptionFactor000088
WBTranscriptionFactor000087
Experimental_infoRNAi_resultWBRNAi00018816Inferred_automaticallyRNAi_primary
WBRNAi00061886Inferred_automaticallyRNAi_primary
WBRNAi00115841Inferred_automaticallyRNAi_primary
WBRNAi00027699Inferred_automaticallyRNAi_primary
WBRNAi00115664Inferred_automaticallyRNAi_primary
WBRNAi00053490Inferred_automaticallyRNAi_primary
WBRNAi00090663Inferred_automaticallyRNAi_primary
Expr_patternExpr701
Expr1019202
Expr1031605
Expr1157055
Expr2013837
Expr2032077
Drives_constructWBCnstr00012497
WBCnstr00036082
Construct_productWBCnstr00021771
WBCnstr00036082
Microarray_results (20)
Expression_cluster (116)
SAGE_tagSAGE:ctcgagaacaStrandSense
Unambiguously_mapped
SAGE:taaataatatStrandAntisense
SAGE:catacacggtagttattStrandAntisense
SAGE:catacacggtStrandAntisense
SAGE:ctcgagaacagcacaacStrandSense
Unambiguously_mapped
SAGE:ctcaataatgtaatgtaStrandSense
Unambiguously_mapped
SAGE:ctcaataatgStrandSense
Unambiguously_mapped
SAGE:taaaataactStrandAntisense
SAGE:ccgcttcggaStrandAntisense
Interaction (12)
Map_infoMapVPosition3.0135Error0.004779
PositivePositive_cloneT19B10Author_evidenceYuan JY
Cole MD
Inferred_automaticallyFrom sequence, transcript, pseudogene data
Mapping_dataMulti_point4855
4822
4225
4437
Pseudo_map_position
Reference (15)
RemarkData extracted from Yuan et al. (1998)
Old name connection to max-1 removed according to [Huang X, Jin Y]. [krb 020614]
Map 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