Genomics
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3 Alleles
DB identifier | Symbol | Allele Class | Organism |
---|---|---|---|
FBal0201729 | CG17036[GD1105] | Drosophila melanogaster | |
FBal0234086 | CG17036[KK106227] | Drosophila melanogaster | |
FBal0272497 | CG17036[NIG.17036R] | Drosophila melanogaster |
5 Clones
Secondary Identifier | DB identifier |
---|---|
CK01.25C.C11 | FBcl0404863 |
AT31745 | FBcl0041811 |
RE26232 | FBcl0204914 |
RE51609 | FBcl0204915 |
RE23324 | FBcl0204917 |
4 Exons
DB identifier | Symbol |
---|---|
FBgn0032449:3 | CG17036:3 |
FBgn0032449:1 | CG17036:1 |
FBgn0032449:2 | CG17036:2 |
FBgn0032449:4 | CG17036:4 |
4 UTRs
Class | DB identifier |
Organism . Name |
---|---|---|
FivePrimeUTR | FBtr0080408-5-prime-utr | Drosophila melanogaster |
FivePrimeUTR | FBtr0340545-5-prime-utr | Drosophila melanogaster |
ThreePrimeUTR | FBtr0080408-3-prime-utr | Drosophila melanogaster |
ThreePrimeUTR | FBtr0340545-3-prime-utr | Drosophila melanogaster |
Other
24 Pathways
- Defective MMAA causes methylmalonic aciduria type cblA,
- Metabolism of water-soluble vitamins and cofactors,
- Vitamin B1 (thiamin) metabolism,
- Defects in biotin (Btn) metabolism,
- Disease,
- Defective BTD causes biotidinase deficiency,
- Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD,
- Defective CUBN causes hereditary megaloblastic anemia 1,
- Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF,
- Defective HLCS causes multiple carboxylase deficiency,
- Defective MUT causes methylmalonic aciduria mut type,
- Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC,
- Defective GIF causes intrinsic factor deficiency,
- Defective AMN causes hereditary megaloblastic anemia 1,
- Metabolism of vitamins and cofactors,
- Defective MTR causes methylmalonic aciduria and homocystinuria type cblG,
- Metabolism of folate and pterines,
- Defects in cobalamin (B12) metabolism,
- Defective MMAB causes methylmalonic aciduria type cblB,
- Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE,
- Defective CD320 causes methylmalonic aciduria,
- Defects in vitamin and cofactor metabolism,
- Defective TCN2 causes hereditary megaloblastic anemia,
- Metabolism
1 Cross References
Identifier |
Source . Name |
Subject . Primary Identifier |
---|---|---|
34679 | NCBI Entrez Gene identifiers | FBgn0032449 |
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
2 Introns
DB identifier |
Organism . Name |
---|---|
intron_FBgn0032449:3_FBgn0032449:1 | Drosophila melanogaster |
intron_FBgn0032449:4_FBgn0032449:2 | Drosophila melanogaster |
11 RNAi Results
Screen | Gene | Phenotype | Score | Conditions | PubMed ID |
---|---|---|---|---|---|
Lipid storage | CG17036 | none | 1.760374603 | 19067489 | |
Lipid storage | CG17036 | none | 1.525592687 | 19067489 | |
Cell size and cell-cycle regulation (1) | CG17036 | none | sp | 16496002 | |
Muscle morphogenesis and function (1) | CG17036 | none | np | 20220848 | |
Heart development and function (1) | CG17036 | none | 1 | 20371351 | |
Serratia marcescens infection (1) | CG17036 | none | -0.136986301369863 | 19520911 | |
Serratia marcescens infection (1) | CG17036 | none | 0.461538461538461 | 19520911 | |
Notch pathway regulation (4) | CG17036 | none | 0 | 19363474 | |
Adiposity regulation (1) | CG17036 | none | 0.056 | 20074523 | |
Hippo pathway regulation | CG17036 | none | -0.38 | 23263283 | |
Glycosylation regulation (1) | CG17036 | none | sp | 21203496 |