Genomics
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5 Alleles
| DB identifier | Symbol | Allele Class | Organism |
|---|---|---|---|
| FBal0160974 | CG7882[f05479] | Drosophila melanogaster | |
| FBal0259809 | CG7882[KK109827] | Drosophila melanogaster | |
| FBal0249230 | CG7882[MI01658] | Drosophila melanogaster | |
| FBal0205644 | CG7882[GD3480] | Drosophila melanogaster | |
| FBal0275758 | CG7882[NIG.7882R] | Drosophila melanogaster |
9 Clones
| Secondary Identifier | DB identifier |
|---|---|
| EP12254 | FBcl0079821 |
| LP07821 | FBcl0188635 |
| IP16073 | FBcl0303849 |
| IP16173 | FBcl0338231 |
| IP16273 | FBcl0340321 |
| IP16373 | FBcl0340322 |
| Dmel_neb_014952_0827_1090 | FBcl0375816 |
| 214247.6 | FBcl0450569 |
| 77577 | FBcl0450558 |
8 Exons
| DB identifier | Symbol |
|---|---|
| FBgn0033047:2 | CG7882:2 |
| FBgn0033047:3 | CG7882:3 |
| FBgn0033047:4 | CG7882:4 |
| FBgn0033047:5 | CG7882:5 |
| FBgn0033047:6 | CG7882:6 |
| FBgn0033047:7 | CG7882:7 |
| FBgn0033047:1 | CG7882:1 |
| FBgn0033047:8 | CG7882:8 |
4 UTRs
| Class | DB identifier |
Organism . Name |
|---|---|---|
| FivePrimeUTR | FBtr0085966-5-prime-utr | Drosophila melanogaster |
| FivePrimeUTR | FBtr0335266-5-prime-utr | Drosophila melanogaster |
| ThreePrimeUTR | FBtr0085966-3-prime-utr | Drosophila melanogaster |
| ThreePrimeUTR | FBtr0335266-3-prime-utr | Drosophila melanogaster |
Other
37 Pathways
- Defective BTD causes biotidinase deficiency,
- Regulation of Insulin Secretion,
- Class II GLUTs,
- Integration of energy metabolism,
- Defective MUT causes methylmalonic aciduria mut type,
- SLC-mediated transmembrane transport,
- Defective TCN2 causes hereditary megaloblastic anemia,
- Glucose transport,
- Metabolism,
- Disease,
- Defects in vitamin and cofactor metabolism,
- Defects in cobalamin (B12) metabolism,
- Hexose uptake,
- Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD,
- Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC,
- Defective MTR causes methylmalonic aciduria and homocystinuria type cblG,
- Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds,
- Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE,
- Defects in biotin (Btn) metabolism,
- Facilitative Na+-independent glucose transporters,
- Regulation of beta-cell development,
- Carbohydrate metabolism,
- Regulation of gene expression in beta cells,
- Defective MMAB causes methylmalonic aciduria type cblB,
- Defective CUBN causes hereditary megaloblastic anemia 1,
- Metabolism of vitamins and cofactors,
- Defective AMN causes hereditary megaloblastic anemia 1,
- Defective GIF causes intrinsic factor deficiency,
- Transmembrane transport of small molecules,
- Defective CD320 causes methylmalonic aciduria,
- Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF,
- Developmental Biology,
- Defective HLCS causes multiple carboxylase deficiency,
- Transcriptional Regulation of White Adipocyte Differentiation,
- Defective MMAA causes methylmalonic aciduria type cblA,
- Metabolism of water-soluble vitamins and cofactors,
- Vitamin C (ascorbate) metabolism
1 Cross References
| Identifier |
Source . Name |
Subject . Primary Identifier |
|---|---|---|
| 35520 | NCBI Entrez Gene identifiers | FBgn0033047 |
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
7 Introns
13 RNAi Results
| Screen | Gene | Phenotype | Score | Conditions | PubMed ID |
|---|---|---|---|---|---|
| Lipid storage | CG7882 | none | -0.242834976 | 19067489 | |
| Lipid storage | CG7882 | none | 0.018426245 | 19067489 | |
| Cell size and cell-cycle regulation (1) | CG7882 | none | sp | 16496002 | |
| Muscle morphogenesis and function (1) | CG7882 | none | np | 20220848 | |
| Muscle morphogenesis and function (1) | CG7882 | none | np | 20220848 | |
| Heat nociception (1) | CG7882 | none | -1.17 | 21074052 | |
| Heart development and function (1) | CG7882 | none | 1 | 20371351 | |
| Serratia marcescens infection (1) | CG7882 | Decreased viability after Serratia marcescens infection | -2.96052631578947 | 19520911 | |
| Notch pathway regulation (4) | CG7882 | none | 0 | 19363474 | |
| Notch pathway regulation (4) | CG7882 | none | 0 | 19363474 | |
| Adiposity regulation (1) | CG7882 | none | -0.317 | 20074523 | |
| Hippo pathway regulation | CG7882 | none | 0.89 | 23263283 | |
| Glycosylation regulation (1) | CG7882 | none | sp | 21203496 |
