WormBase Tree Display for Gene: WBGene00008132
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WBGene00008132 | SMap | S_parent | Sequence | C47B2 | |||
---|---|---|---|---|---|---|---|
Identity | Version | 2 | |||||
Name | CGC_name | gale-1 | Person_evidence | WBPerson2629 | |||
WBPerson1805 | |||||||
Sequence_name | C47B2.6 | ||||||
Molecular_name | C47B2.6a | ||||||
C47B2.6a.1 | |||||||
CE17566 | |||||||
C47B2.6b | |||||||
CE38295 | |||||||
C47B2.6a.2 | |||||||
C47B2.6b.1 | |||||||
C47B2.6b.2 | |||||||
Other_name | CELE_C47B2.6 | Accession_evidence | NDB | BX284601 | |||
Public_name | gale-1 | ||||||
DB_info | Database (12) | ||||||
Species | Caenorhabditis elegans | ||||||
History | Version_change (2) | ||||||
Status | Live | ||||||
Gene_info | Biotype | SO:0001217 | |||||
Gene_class | gale | ||||||
Allele (158) | |||||||
Strain | WBStrain00002441 | ||||||
WBStrain00001620 | |||||||
RNASeq_FPKM (74) | |||||||
GO_annotation (29) | |||||||
Contained_in_operon | CEOP1786 | ||||||
Ortholog (38) | |||||||
Paralog (13) | |||||||
Structured_description (2) | |||||||
Disease_info | Experimental_model | DOID:9870 | Homo sapiens | Paper_evidence | WBPaper00045849 | ||
Accession_evidence | OMIM | 230350 | |||||
Curator_confirmed | WBPerson324 | ||||||
Date_last_updated | 03 Oct 2018 00:00:00 | ||||||
Potential_model | DOID:0111458 | Homo sapiens | Inferred_automatically | Inferred by orthology to human genes with DO annotation (HGNC:4116) | |||
Disease_relevance | Mutations 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 intermediates | Homo sapiens | Paper_evidence | WBPaper00045849 | |||
Accession_evidence | OMIM | 606953 | |||||
Curator_confirmed | WBPerson324 | ||||||
Models_disease_in_annotation | WBDOannot00000322 | ||||||
Molecular_info | Corresponding_CDS | C47B2.6a | |||||
C47B2.6b | |||||||
Corresponding_transcript | C47B2.6a.1 | ||||||
C47B2.6a.2 | |||||||
C47B2.6b.1 | |||||||
C47B2.6b.2 | |||||||
Other_sequence (191) | |||||||
Associated_feature | WBsf657001 | ||||||
WBsf657002 | |||||||
WBsf218666 | |||||||
WBsf218667 | |||||||
WBsf218668 | |||||||
WBsf218669 | |||||||
Experimental_info | RNAi_result | WBRNAi00042653 | Inferred_automatically | RNAi_primary | |||
WBRNAi00003176 | Inferred_automatically | RNAi_primary | |||||
WBRNAi00029897 | Inferred_automatically | RNAi_primary | |||||
Expr_pattern | Expr5525 | ||||||
Expr5526 | |||||||
Expr1017938 | |||||||
Expr1033529 | |||||||
Expr1146641 | |||||||
Expr2011938 | |||||||
Expr2030175 | |||||||
Drives_construct | WBCnstr00002459 | ||||||
WBCnstr00004348 | |||||||
Construct_product | WBCnstr00019730 | ||||||
Microarray_results (25) | |||||||
Expression_cluster (209) | |||||||
Interaction (62) | |||||||
WBProcess | WBbiopr:00000046 | ||||||
Map_info | Map | I | Position | 16.8109 | Error | 0.002729 | |
Positive | Positive_clone | C47B2 | Inferred_automatically | From sequence, transcript, pseudogene data | |||
Pseudo_map_position | |||||||
Reference | WBPaper00027024 | ||||||
WBPaper00028564 | |||||||
WBPaper00029024 | |||||||
WBPaper00036792 | |||||||
WBPaper00038491 | |||||||
WBPaper00045849 | |||||||
WBPaper00055090 | |||||||
WBPaper00062922 | |||||||
WBPaper00064651 | |||||||
Remark | 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 | |||||
Method | Gene |