Genomics
Gene Ontology Displayer
Homologue Displayer
Mod Mine G Browse Displayer
Overlapping Features Displayer
Regulatory Regions Displayer
5 Alleles
DB identifier | Symbol | Allele Class | Organism |
---|---|---|---|
FBal0259023 | CG2543[KK101788] | Drosophila melanogaster | |
FBal0131536 | CG2543[PG44] | Drosophila melanogaster | |
FBal0202315 | CG2543[GD9789] | Drosophila melanogaster | |
FBal0221885 | CG2543[EY00581] | Drosophila melanogaster | |
FBal0273143 | CG2543[NIG.2543R] | Drosophila melanogaster |
16 Clones
5 Exons
DB identifier | Symbol |
---|---|
FBgn0030407:1 | CG2543:1 |
FBgn0030407:2 | CG2543:2 |
FBgn0030407:3 | CG2543:3 |
FBgn0030407:4 | CG2543:4 |
FBgn0030407:5 | CG2543:5 |
2 UTRs
Class | DB identifier |
Organism . Name |
---|---|---|
FivePrimeUTR | FBtr0073655-5-prime-utr | Drosophila melanogaster |
ThreePrimeUTR | FBtr0073655-3-prime-utr | Drosophila melanogaster |
Other
23 Pathways
- Metabolism of water-soluble vitamins and cofactors,
- Defective CD320 causes methylmalonic aciduria,
- Metabolism,
- Metabolism of folate and pterines,
- Defective BTD causes biotidinase deficiency,
- Defective GIF causes intrinsic factor deficiency,
- Defective MMAA causes methylmalonic aciduria type cblA,
- Defects in biotin (Btn) metabolism,
- Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD,
- Defective MMAB causes methylmalonic aciduria type cblB,
- Metabolism of vitamins and cofactors,
- Defects in cobalamin (B12) metabolism,
- Defects in vitamin and cofactor metabolism,
- Defective CUBN causes hereditary megaloblastic anemia 1,
- Defective MUT causes methylmalonic aciduria mut type,
- Defective MTR causes methylmalonic aciduria and homocystinuria type cblG,
- Defective HLCS causes multiple carboxylase deficiency,
- Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE,
- Disease,
- Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC,
- Defective AMN causes hereditary megaloblastic anemia 1,
- Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF,
- Defective TCN2 causes hereditary megaloblastic anemia
1 Cross References
Identifier |
Source . Name |
Subject . Primary Identifier |
---|---|---|
32212 | NCBI Entrez Gene identifiers | FBgn0030407 |
9 Data Sets
Name | URL |
---|---|
FlyBase data set for Drosophila melanogaster | |
TrEMBL data set | http://www.ebi.ac.uk/trembl/ |
Drosophila 12 Genomes Consortium homology | |
GenomeRNAi data set | |
TreeFam data set | |
Panther data set | |
GO Annotation from FlyBase | |
FlyBase fasta data set for Drosophila melanogaster | |
Drosophila Cell Line and Developmental Stage Gene and Exon Scores |
55 Expression Scores
12 RNAi Results
Screen | Gene | Phenotype | Score | Conditions | PubMed ID |
---|---|---|---|---|---|
Lipid storage | CG2543 | none | -0.027052385 | 19067489 | |
Lipid storage | CG2543 | none | -0.237785425 | 19067489 | |
Lipid storage | CG2543 | none | -0.524307797 | 19067489 | |
Cell size and cell-cycle regulation (1) | CG2543 | none | sp | 16496002 | |
Muscle morphogenesis and function (1) | CG2543 | none | np | 20220848 | |
Heat nociception (1) | CG2543 | none | -0.67 | 21074052 | |
Heart development and function (1) | CG2543 | none | 0.75 | 20371351 | |
Heart development and function (2) | CG2543 | none | 2.89 | 20371351 | |
Serratia marcescens infection (1) | CG2543 | none | 0.175 | 19520911 | |
Notch pathway regulation (4) | CG2543 | none | 0 | 19363474 | |
Adiposity regulation (1) | CG2543 | none | -0.078 | 20074523 | |
Glycosylation regulation (1) | CG2543 | none | sp | 21203496 |