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WormBase Tree Display for Gene: WBGene00016144

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Name Class

WBGene00016144SMapS_parentSequenceC26E6
IdentityVersion3
Name (5)
DB_infoDatabase (11)
SpeciesCaenorhabditis elegans
HistoryVersion_change128 May 2004 13:30:57WBPerson1971EventImportedInitial conversion from CDS class of stlace from WS125
221 Jun 2005 09:45:25WBPerson2970Name_changeCGC_nametag-339
316 Jan 2006 17:59:10WBPerson2970Name_changeCGC_namemmab-1
Other_nametag-339
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classmmab
Allele (18)
RNASeq_FPKM (74)
GO_annotation00060522
00060523
00060524
00060525
00060526
00060527
Contained_in_operonCEOP3240
Ortholog (32)
Structured_descriptionConcise_descriptionmmab-1 encodes an ortholog of human co(I)balamin adenosyltransferase (MMAB); mmab-1 deletion mutants incorporate abnormally low levels of 1-[(14)C]-propionate into proteins; mmab-1 mutants and mmab-1(RNAi) animals excrete abnormally high levels of methylmalonic acid into their culture medium when challenged with propionic acid; these data are consistent with the hypothesis that MMAB-1 participates in the conversion of propionyl-CoA to succinyl-CoA.Paper_evidenceWBPaper00027754
Curator_confirmedWBPerson567
Date_last_updated02 Oct 2006 00:00:00
Automated_descriptionPredicted to enable corrinoid adenosyltransferase activity. Used to study methylmalonic acidemia. Human ortholog(s) of this gene implicated in methylmalonic acidemia cblB type. Is an ortholog of human MMAB (metabolism of cobalamin associated B).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:14749Homo sapiensPaper_evidenceWBPaper00027754
Accession_evidenceOMIM251000
251100
Curator_confirmedWBPerson324
Date_last_updated29 May 2014 00:00:00
Potential_modelDOID:0060743Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19331)
DOID:655Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:19331)
Disease_relevanceMethylmalonic aciduria is a genetically heterogeneous disorder of methylmalonate and cobalamin (vitamin B12) metabolism; the metabolism of propionyl-CoA to succinyl-CoA via the formation and isomerization of methylmalonyl-CoA is a critical metabolic pathway in humans; the defective conversion of L-methylmalonyl-CoA to succinyl-CoA in the mitochondrial matrix causes hereditary methylmalonic acidemias, characterized by the accumulation of methylmalonic acid in tissues and secondary metabolic perturbations such as hyperglycinemia and hyperammonemia; affected individuals may suffer from developmental delay, renal disease, pancreatitis and metabolic infarction of the basal ganglia; C.elegans expresses the full complement of mammalian homologues for the conversion of propionyl-CoA to succinyl-CoA, including propionyl-CoA carboxylase subunits A and B (pcca-1,pccb-1), methylmalonic acidemia cobalamin A complementation group (mmaa-1), co(I)balaminadenosyltransferase (mmab-1), MMACHC (cblc-1), methylmalonyl-CoA epimerase (mce-1) and methylmalonyl-CoA mutase (mmcm-1); deletion mutants of mmcm-1(ok1637), mmab-1(ok1484 and ok1493) and mce-1(ok243) displayed reduced 1-[14C]-propionate incorporation into macromolecules and produced increased amounts of methylmalonic acid in the culture medium, proving that a functional block in the pathway caused metabolite accumulation; lentiviral delivery of the C. elegans mmcm-1 into fibroblasts derived from a patient with mut class methylmalonic acidemia could partially restore propionate flux; the C. elegans mce-1 deletion mutant demonstrates for the first time that a lesion at the epimerase step of methylmalonyl-CoA metabolism can functionally impair flux through the methylmalonyl-CoA mutase pathway and suggests that malfunction of MCEE may cause methylmalonic acidemia in humans.Homo sapiensPaper_evidenceWBPaper00027754
Accession_evidenceOMIM251000
251100
607568
Curator_confirmedWBPerson324
Date_last_updated29 May 2014 00:00:00
Models_disease_in_annotationWBDOannot00000285
Molecular_infoCorresponding_CDSC26E6.11
Corresponding_CDS_historyC26E6.11:wp152
Corresponding_transcriptC26E6.11.1
C26E6.11.2
Other_sequence (31)
Associated_featureWBsf651018
WBsf666834
WBsf666835
WBsf666836
WBsf666837
WBsf226609
WBsf226610
Experimental_infoRNAi_resultWBRNAi00067760Inferred_automaticallyRNAi_primary
WBRNAi00076161Inferred_automaticallyRNAi_primary
WBRNAi00011212Inferred_automaticallyRNAi_primary
WBRNAi00002187Inferred_automaticallyRNAi_primary
WBRNAi00078225Inferred_automaticallyRNAi_primary
WBRNAi00005233Inferred_automaticallyRNAi_primary
WBRNAi00007907Inferred_automaticallyRNAi_primary
WBRNAi00041267Inferred_automaticallyRNAi_primary
Expr_patternExpr1020305
Expr1036905
Expr1145309
Expr2013625
Expr2031859
Drives_constructWBCnstr00028295
Construct_productWBCnstr00028295
Microarray_results (20)
Expression_clusterWBPaper00031040:TGF-beta_adult_downregulated
WBPaper00032031:DConiospora_upregulated_cDNA_24h
WBPaper00033065:cyc-1(RNAi)_downregulated
WBPaper00033065:isp-1-1(qm150)_upregulated
WBPaper00037950:all-neurons_L2-larva_expressed
WBPaper00037950:bodywall-muscle_L2-larva_expressed
WBPaper00037950:CEP-sheath-cells_Day1-adult_expressed
WBPaper00037950:coelomocytes_L2-larva_expressed
WBPaper00037950:dopaminergic-neurons_L3-L4-larva_expressed
WBPaper00037950:excretory-cell_L2-larva_expressed
WBPaper00037950:GABAergic-motor-neurons_L2-larva_expressed
WBPaper00037950:hypodermis_L3-L4-larva_expressed
WBPaper00037950:hypodermis_larva_enriched
WBPaper00037950:intestine_L1-larva_expressed
WBPaper00037950:intestine_L2-larva_expressed
WBPaper00037950:PVD-OLL-neurons_L3-L4-larva_expressed
WBPaper00040560:hpl-2_embryo_downregulated
WBPaper00044426:rotenone_24h_upregulated
WBPaper00044501:gld-1_let-7_regulated
WBPaper00044736:flat_dev_expression
WBPaper00045521:Gender_Neutral
WBPaper00045729:gld-2(RNAi)_downregulated
WBPaper00048988:neuron_expressed
WBPaper00049545:jmjd-3.1(+)_downregulated
WBPaper00050344:PLM-neuron_enriched
WBPaper00050488:20C_vs_25C_regulated_mir-34(OverExpression)_adult
WBPaper00050488:20C_vs_25C_regulated_N2_adult
WBPaper00050488:adult_vs_dauer_regulated_N2_20C
WBPaper00050488:mir-34(gk437)_vs_mir-34(OverExpression)_regulated_dauer_20C
WBPaper00050488:N2_vs_mir-34(gk437)_regulated_dauer_20C
WBPaper00050726:OsmoticStress_regulated_Food
WBPaper00050726:OsmoticStress_regulated_NoFood
WBPaper00050859:downregulated_P-granule(-)GFP(+)_vs_control_day2-adult
WBPaper00050990:GABAergic-neuron_expressed
WBPaper00050990:hypodermis_expressed
WBPaper00050990:intestine_expressed
WBPaper00050990:seam_expressed
WBPaper00053184:sma-2(rax5)_downregulated
WBPaper00053184:sma-4(rax3)_downregulated
WBPaper00053302:zidovudine_72h_regulated
WBPaper00053321:nos-1(gv5)nos-2(RNAi)_downregulated_L1_SMARTseq
WBPaper00053321:PGCs_enriched_NuGen
WBPaper00053388:dauer_regulated_Cluster5
WBPaper00053810:daf-2(e1370)_downregulated
WBPaper00055648:germline_expressed
WBPaper00055862:antimycin_damt-1(gk961032)_regulated
WBPaper00056090:E.faecalis_downregulated_N2
WBPaper00056161:male_enriched_siRNA
WBPaper00056471:S.aureus-4h_downregulated_N2
WBPaper00057288:iff-1(RNAi)_downregulated_transcript
WBPaper00059328:mrps-5(RNAi)_upregulated_mRNA
WBPaper00059356:BAZ-2_SET-6_interacting
WBPaper00060014:set-2(tm1630)_upregulated
WBPaper00060100:SiNP_downregulated_mRNA
WBPaper00061340:RID_parent
WBPaper00061527:F31C3.4_6048-cutc-1_15804
WBPaper00062325:muscle_enriched_coding-RNA
WBPaper00062345:bortezomib_4h_upregulated_N2
WBPaper00062498:PPM-1.D_interacting
WBPaper00062554:MAGU-2_interacting
WBPaper00064071:NHR-49_interacting
WBPaper00064716:paraquat_upregulated
cgc4386_cluster_3_5
cgc4489_group_4
WBPaper00025032:cluster_8
WBPaper00025141:N2_Expressed_Genes
WBPaper00025141:unc-4::GFP_Expressed_Genes
WBPaper00026929:Resveratrol_regulated_daf-16
WBPaper00026929:sir-2.1_overexpression_regulated
WBPaper00026980:intestine_enriched
WBPaper00031003:24hr_muscle_enriched
WBPaper00031003:total_muscle_enriched
WBPaper00035084:embryo_enriched_AIN-2_IP
WBPaper00035905:FBF-1_Associated
WBPaper00036123:Fluoranthene_regulated
WBPaper00037147:heatshock_upregulated
WBPaper00040858:eQTL_age_regulated_developing
WBPaper00041606:CE_X.nematophila_regulated
WBPaper00041939:EtBr-exposed_vs_UVC-exposed_48h
WBPaper00041939:UVC-EtBr-exposed_vs_UVC-exposed_51h
WBPaper00045263:0.1mM-paraquat_upregulated
WBPaper00045263:isp-1(qm150)_upregulated
WBPaper00045263:nuo-6(qm200)_upregulated
WBPaper00045263:ProLongevity-mtROS_upregulated
WBPaper00045960:L1-L4-lethargus_downregulated
WBPaper00045960:L4-lethargus_downregulated
WBPaper00048989:eat-2(ad465)_rapamycin_upregulated
WBPaper00048989:N2_allantoin_upregulated
WBPaper00053236:Starvation_regulated_GR1307
[cgc5767]:cluster_6
[cgc5767]:expression_class_M
[cgc5767]:expression_class_MD
[cgc5767]:expression_class_MD_pd(23_min)
[cgc5767]:expression_class_SM
[cgc5767]:expression_class_SMD
[cgc6390]:mixed_oogenesis-somatic
InteractionWBInteraction000007214
WBInteraction000173906
WBInteraction000552627
WBInteraction000553755
Map_infoMapIIIPosition-2.35895Error0.002868
PositivePositive_cloneC26E6Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027754
WBPaper00038491
WBPaper00045654
WBPaper00049923
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