Genomics
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13 Alleles
DB identifier | Symbol | Allele Class | Organism |
---|---|---|---|
FBal0154376 | v(2)k05816[EY01808] | Drosophila melanogaster | |
FBal0177272 | v(2)k05816[f02758] | Drosophila melanogaster | |
FBal0177275 | v(2)k05816[d04154] | Drosophila melanogaster | |
FBal0177273 | v(2)k05816[f02757] | Drosophila melanogaster | |
FBal0118032 | v(2)k05816[k05816] | Drosophila melanogaster | |
FBal0177274 | v(2)k05816[e00126] | Drosophila melanogaster | |
FBal0177276 | v(2)k05816[c07138] | Drosophila melanogaster | |
FBal0128970 | v(2)k05816[EP695] | Drosophila melanogaster | |
FBal0247758 | v(2)k05816[MI01528] | Drosophila melanogaster | |
FBal0210849 | v(2)k05816[GD1555] | Drosophila melanogaster | |
FBal0222113 | v(2)k05816[NP0131] | Drosophila melanogaster | |
FBal0234243 | v(2)k05816[KK106426] | Drosophila melanogaster | |
FBal0273854 | v(2)k05816[NIG.3524R] | Drosophila melanogaster |
7 Clones
Secondary Identifier | DB identifier |
---|---|
GH22259 | FBcl0110023 |
GH05495 | FBcl0132543 |
GH02912 | FBcl0135245 |
GH16082 | FBcl0135249 |
LP13874 | FBcl0190486 |
SD03777 | FBcl0275242 |
AT10488 | FBcl0296976 |
10 Exons
DB identifier | Symbol |
---|---|
FBgn0042627:2 | v(2)k05816:2 |
FBgn0042627:3 | v(2)k05816:3 |
FBgn0042627:4 | v(2)k05816:4 |
FBgn0042627:5 | v(2)k05816:5 |
FBgn0042627:7 | v(2)k05816:7 |
FBgn0042627:8 | v(2)k05816:8 |
FBgn0042627:9 | v(2)k05816:9 |
FBgn0042627:1 | v(2)k05816:1 |
FBgn0042627:6 | v(2)k05816:6 |
FBgn0042627:10 | v(2)k05816:10 |
4 UTRs
Class | DB identifier |
Organism . Name |
---|---|---|
FivePrimeUTR | FBtr0077657-5-prime-utr | Drosophila melanogaster |
FivePrimeUTR | FBtr0335386-5-prime-utr | Drosophila melanogaster |
ThreePrimeUTR | FBtr0077657-3-prime-utr | Drosophila melanogaster |
ThreePrimeUTR | FBtr0335386-3-prime-utr | Drosophila melanogaster |
Other
46 Pathways
- Metabolism of water-soluble vitamins and cofactors,
- Fructose catabolism,
- Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF,
- ChREBP activates metabolic gene expression,
- Carbohydrate metabolism,
- Regulation of gene expression in beta cells,
- Defective MTR causes methylmalonic aciduria and homocystinuria type cblG,
- Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD,
- Defective CD320 causes methylmalonic aciduria,
- SLC-mediated transmembrane transport,
- Activation of Gene Expression by SREBP (SREBF),
- Metabolism of lipids and lipoproteins,
- Glucose metabolism,
- Coenzyme A biosynthesis,
- Defects in biotin (Btn) metabolism,
- Defective GIF causes intrinsic factor deficiency,
- Pentose phosphate pathway (hexose monophosphate shunt),
- Defective AMN causes hereditary megaloblastic anemia 1,
- Transmembrane transport of small molecules,
- Defective MUT causes methylmalonic aciduria mut type,
- Metabolism,
- Defective HLCS causes multiple carboxylase deficiency,
- Metabolism of vitamins and cofactors,
- Regulation of beta-cell development,
- Vitamin B5 (pantothenate) metabolism,
- Defective TCN2 causes hereditary megaloblastic anemia,
- Glucose transport,
- Defective MMAA causes methylmalonic aciduria type cblA,
- Fatty Acyl-CoA Biosynthesis,
- Regulation of Cholesterol Biosynthesis by SREBP (SREBF),
- Hexose uptake,
- Developmental Biology,
- Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC,
- Defective CUBN causes hereditary megaloblastic anemia 1,
- PP2A-mediated dephosphorylation of key metabolic factors,
- Triglyceride Biosynthesis,
- Defective BTD causes biotidinase deficiency,
- Glycolysis,
- Integration of energy metabolism,
- Disease,
- Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE,
- Insulin effects increased synthesis of Xylulose-5-Phosphate,
- Defects in vitamin and cofactor metabolism,
- Defects in cobalamin (B12) metabolism,
- Defective MMAB causes methylmalonic aciduria type cblB,
- Fatty acid, triacylglycerol, and ketone body metabolism
2 Cross References
Identifier |
Source . Name |
Subject . Primary Identifier |
---|---|---|
117361 | NCBI Entrez Gene identifiers | FBgn0042627 |
72883 | BioGRID | FBgn0042627 |
11 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 | |
IntAct interactions data set | |
BioGRID interaction data set | http://www.thebiogrid.org/downloads.php |
GO Annotation from FlyBase | |
FlyBase fasta data set for Drosophila melanogaster | |
Drosophila Cell Line and Developmental Stage Gene and Exon Scores |
55 Expression Scores
10 Introns
17 RNAi Results
Screen | Gene | Phenotype | Score | Conditions | PubMed ID |
---|---|---|---|---|---|
Lipid storage | v(2)k05816 | none | 1.033021216 | 19067489 | |
Lipid storage | v(2)k05816 | none | -0.020776512 | 19067489 | |
Lipid storage | v(2)k05816 | none | -0.009244328 | 19067489 | |
Lipid storage | v(2)k05816 | none | 0.200747201 | 19067489 | |
Cell size and cell-cycle regulation (1) | v(2)k05816 | none | sp | 16496002 | |
Muscle morphogenesis and function (1) | v(2)k05816 | none | np | 20220848 | |
Muscle morphogenesis and function (1) | v(2)k05816 | none | np | 20220848 | |
Heat nociception (1) | v(2)k05816 | none | -0.92 | 21074052 | |
Heart development and function (1) | v(2)k05816 | none | 1 | 20371351 | |
Heart development and function (1) | v(2)k05816 | none | 1 | 20371351 | |
Serratia marcescens infection (1) | v(2)k05816 | none | 0.6 | 19520911 | |
Notch pathway regulation (4) | v(2)k05816 | none | 0 | 19363474 | |
Notch pathway regulation (4) | v(2)k05816 | none | 0 | 19363474 | |
PGN-induced dJNK phosphorylation | v(2)k05816 | Increased P-JNK protein expression with PGN | 2.34 | 15 min PGN induction | 19893628 |
Adiposity regulation (1) | v(2)k05816 | none | -0.292 | 20074523 | |
Hippo pathway regulation | v(2)k05816 | none | 0.05 | 23263283 | |
Glycosylation regulation (1) | v(2)k05816 | none | sp | 21203496 |