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WormBase Tree Display for Gene: WBGene00008132

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Name Class

WBGene00008132SMapS_parentSequenceC47B2
IdentityVersion2
NameCGC_namegale-1Person_evidenceWBPerson2629
WBPerson1805
Sequence_nameC47B2.6
Molecular_nameC47B2.6a
C47B2.6a.1
CE17566
C47B2.6b
CE38295
C47B2.6a.2
C47B2.6b.1
C47B2.6b.2
Other_nameCELE_C47B2.6Accession_evidenceNDBBX284601
Public_namegale-1
DB_infoDatabase (12)
SpeciesCaenorhabditis elegans
HistoryVersion_change126 May 2004 16:54:48WBPerson1971EventImportedInitial conversion from CDS class of WS125
202 Feb 2007 17:11:41WBPerson2970Name_changeCGC_namegale-1
StatusLive
Gene_infoBiotypeSO:0001217
Gene_classgale
Allele (158)
StrainWBStrain00002441
WBStrain00001620
RNASeq_FPKM (74)
GO_annotation (29)
Contained_in_operonCEOP1786
Ortholog (38)
Paralog (13)
Structured_descriptionConcise_descriptiongale-1 encodes a putative UDP-galactose-4-epimerase, orthologous tohuman GALE (OMIM:606953, mutated in galactose epimerase deficiency);GALE-1 is thought to interconvert UDP-N-acetylglucosamine andUDP-N-acetylgalactosamine at the end of the hexosamine pathway; gale-1is expressed in neurons, intestine and the developing reproductivesystem, but has no observed function in mass RNAi assays.Paper_evidenceWBPaper00006525
WBPaper00028588
Curator_confirmedWBPerson1823
WBPerson567
Date_last_updated07 Apr 2007 00:00:00
Automated_descriptionEnables UDP-N-acetylglucosamine 4-epimerase activity and UDP-glucose 4-epimerase activity. Involved in several processes, including gonad morphogenesis; negative regulation of endoplasmic reticulum unfolded protein response; and positive regulation of vulval development. Predicted to be located in cytosol. Expressed in head. Used to study galactosemia. Human ortholog(s) of this gene implicated in galactose epimerase deficiency. Is an ortholog of human GALE (UDP-galactose-4-epimerase).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:9870Homo sapiensPaper_evidenceWBPaper00045849
Accession_evidenceOMIM230350
Curator_confirmedWBPerson324
Date_last_updated03 Oct 2018 00:00:00
Potential_modelDOID:0111458Homo sapiensInferred_automaticallyInferred by orthology to human genes with DO annotation (HGNC:4116)
Disease_relevanceMutations in human GALE (UDP-galactose-4-prime-epimerase) are implicated in the autosomal recessive disorder, type III galactosemia; GALE participates in the galactose metabolism pathway, catalyzing the interconversion of UDP-galactose (UDP-gal) and UDP-glucose (UDP-glc) and in some species, including humans, also the interconversion of UDP-N-acetylgalactosamine (UDP-galNAc) and UDP-N-acetylglucosamine (UDP-glcNAc; one of the symptoms of galactosemia is intolerance to a galactose-rich diet, attributed to the accumulation of toxic galactose metabolism intermediatesHomo sapiensPaper_evidenceWBPaper00045849
Accession_evidenceOMIM606953
Curator_confirmedWBPerson324
Models_disease_in_annotationWBDOannot00000322
Molecular_infoCorresponding_CDSC47B2.6a
C47B2.6b
Corresponding_transcriptC47B2.6a.1
C47B2.6a.2
C47B2.6b.1
C47B2.6b.2
Other_sequence (191)
Associated_featureWBsf657001
WBsf657002
WBsf218666
WBsf218667
WBsf218668
WBsf218669
Experimental_infoRNAi_resultWBRNAi00042653Inferred_automaticallyRNAi_primary
WBRNAi00003176Inferred_automaticallyRNAi_primary
WBRNAi00029897Inferred_automaticallyRNAi_primary
Expr_patternExpr5525
Expr5526
Expr1017938
Expr1033529
Expr1146641
Expr2011938
Expr2030175
Drives_constructWBCnstr00002459
WBCnstr00004348
Construct_productWBCnstr00019730
Microarray_results (25)
Expression_cluster (209)
InteractionWBInteraction000032028
WBInteraction000048528
WBInteraction000103922
WBInteraction000104244
WBInteraction000172107
WBInteraction000190697
WBInteraction000191337
WBInteraction000214949
WBInteraction000232566
WBInteraction000234449
WBInteraction000240917
WBInteraction000241126
WBInteraction000241127
WBInteraction000258492
WBInteraction000261930
WBInteraction000276140
WBInteraction000300279
WBInteraction000305542
WBInteraction000305543
WBInteraction000305544
WBInteraction000305545
WBInteraction000309168
WBInteraction000337700
WBInteraction000337701
WBInteraction000340511
WBInteraction000342286
WBInteraction000349035
WBInteraction000358863
WBInteraction000364322
WBInteraction000377846
WBInteraction000378653
WBInteraction000396852
WBInteraction000401536
WBInteraction000416351
WBInteraction000416927
WBInteraction000429806
WBInteraction000429807
WBInteraction000433172
WBInteraction000458081
WBInteraction000458927
WBInteraction000458928
WBInteraction000462871
WBInteraction000466977
WBInteraction000467574
WBInteraction000468361
WBInteraction000468362
WBInteraction000468363
WBInteraction000469211
WBInteraction000470086
WBInteraction000471526
WBInteraction000471527
WBInteraction000471528
WBInteraction000474028
WBInteraction000514717
WBInteraction000550084
WBInteraction000551775
WBInteraction000563121
WBInteraction000563891
WBInteraction000574885
WBInteraction000579723
WBInteraction000582767
WBInteraction000583186
WBProcessWBbiopr:00000046
Map_infoMapIPosition16.8109Error0.002729
PositivePositive_cloneC47B2Inferred_automaticallyFrom sequence, transcript, pseudogene data
Pseudo_map_position
ReferenceWBPaper00027024
WBPaper00028564
WBPaper00029024
WBPaper00036792
WBPaper00038491
WBPaper00045849
WBPaper00055090
WBPaper00062922
WBPaper00064651
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