Genomics
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3 Alleles
| DB identifier | Symbol | Allele Class | Organism |
|---|---|---|---|
| FBal0146769 | sut3[KG10160] | Drosophila melanogaster | |
| FBal0210711 | sut3[GD1865] | Drosophila melanogaster | |
| FBal0272761 | sut3[NIG.17976R] | Drosophila melanogaster |
9 Clones
| Secondary Identifier | DB identifier |
|---|---|
| AT01738 | FBcl0030043 |
| AT29994 | FBcl0030047 |
| AT02183 | FBcl0030049 |
| AT27196 | FBcl0030051 |
| AT31196 | FBcl0030055 |
| AT05475 | FBcl0030059 |
| EC35236 | FBcl0069323 |
| EK184507 | FBcl0134944 |
| FI08437 | FBcl0474901 |
6 Exons
| DB identifier | Symbol |
|---|---|
| FBgn0028561:1 | sut3:1 |
| FBgn0028561:2 | sut3:2 |
| FBgn0028561:4 | sut3:4 |
| FBgn0028561:5 | sut3:5 |
| FBgn0028561:6 | sut3:6 |
| FBgn0028561:3 | sut3:3 |
4 UTRs
| Class | DB identifier |
Organism . Name |
|---|---|---|
| FivePrimeUTR | FBtr0088779-5-prime-utr | Drosophila melanogaster |
| FivePrimeUTR | FBtr0332247-5-prime-utr | Drosophila melanogaster |
| ThreePrimeUTR | FBtr0088779-3-prime-utr | Drosophila melanogaster |
| ThreePrimeUTR | FBtr0332247-3-prime-utr | Drosophila melanogaster |
Other
37 Pathways
- Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF,
- Defects in vitamin and cofactor metabolism,
- Defective MTR causes methylmalonic aciduria and homocystinuria type cblG,
- Metabolism of vitamins and cofactors,
- Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC,
- Integration of energy metabolism,
- Hexose uptake,
- Transmembrane transport of small molecules,
- Defective AMN causes hereditary megaloblastic anemia 1,
- Defective BTD causes biotidinase deficiency,
- Facilitative Na+-independent glucose transporters,
- Defective TCN2 causes hereditary megaloblastic anemia,
- Regulation of gene expression in beta cells,
- Developmental Biology,
- Class II GLUTs,
- Defective GIF causes intrinsic factor deficiency,
- Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds,
- SLC-mediated transmembrane transport,
- Defective CUBN causes hereditary megaloblastic anemia 1,
- Disease,
- Metabolism of water-soluble vitamins and cofactors,
- Vitamin C (ascorbate) metabolism,
- Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD,
- Regulation of Insulin Secretion,
- Defective HLCS causes multiple carboxylase deficiency,
- Metabolism,
- Carbohydrate metabolism,
- Defective MMAA causes methylmalonic aciduria type cblA,
- Defective CD320 causes methylmalonic aciduria,
- Transcriptional Regulation of White Adipocyte Differentiation,
- Defects in cobalamin (B12) metabolism,
- Glucose transport,
- Defective MMAB causes methylmalonic aciduria type cblB,
- Defective MUT causes methylmalonic aciduria mut type,
- Defects in biotin (Btn) metabolism,
- Regulation of beta-cell development,
- Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
1 Cross References
| Identifier |
Source . Name |
Subject . Primary Identifier |
|---|---|---|
| 44268 | NCBI Entrez Gene identifiers | FBgn0028561 |
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
6 Introns
15 RNAi Results
| Screen | Gene | Phenotype | Score | Conditions | PubMed ID |
|---|---|---|---|---|---|
| Lipid storage | sut3 | none | -0.806521104 | 19067489 | |
| Lipid storage | sut3 | none | 1.266336745 | 19067489 | |
| Constitutive protein secretion and Golgi organization (1) | sut3 | Decreased horseradish peroxidase protein expression | sp | 16452979 | |
| Cell size and cell-cycle regulation (1) | sut3 | none | sp | 16496002 | |
| Mutant human huntingtin aggregation | sut3 | Increased mutant human huntingtin aggregation | 1.5 - 2 | 19789644 | |
| Muscle morphogenesis and function (1) | sut3 | none | np | 20220848 | |
| Heat nociception (1) | sut3 | none | -1.17 | 21074052 | |
| Heart development and function (1) | sut3 | none | 1 | 20371351 | |
| Serratia marcescens infection (1) | sut3 | none | -0.205882352941176 | 19520911 | |
| Notch pathway regulation (4) | sut3 | none | 0 | 19363474 | |
| Adiposity regulation (1) | sut3 | none | -0.405 | 20074523 | |
| Blood cell homeostasis regulation (1) | sut3 | none | np | 20540764 | |
| Blood cell homeostasis regulation (2) | sut3 | none | np | 20540764 | |
| Hippo pathway regulation | sut3 | none | 0.83 | 23263283 | |
| Glycosylation regulation (1) | sut3 | none | sp | 21203496 |
