Genomics
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25 Alleles
11 Clones
Secondary Identifier | DB identifier |
---|---|
IP15954 | FBcl0001582 |
EK290464 | FBcl0090320 |
EK259958 | FBcl0090338 |
EK029310 | FBcl0090374 |
GH16403 | FBcl0114751 |
IP15654 | FBcl0355112 |
IP15754 | FBcl0355113 |
IP15854 | FBcl0355114 |
FGM223H01 | FBcl0390929 |
CK01.34C.C3 | FBcl0444960 |
156824 | FBcl0444948 |
6 Exons
DB identifier | Symbol |
---|---|
FBgn0263241:1 | Mocs1:1 |
FBgn0263241:3 | Mocs1:3 |
FBgn0263241:4 | Mocs1:4 |
FBgn0263241:6 | Mocs1:6 |
FBgn0263241:2 | Mocs1:2 |
FBgn0263241:5 | Mocs1:5 |
4 UTRs
Class | DB identifier |
Organism . Name |
---|---|---|
FivePrimeUTR | FBtr0076204-5-prime-utr | Drosophila melanogaster |
FivePrimeUTR | FBtr0076205-5-prime-utr | Drosophila melanogaster |
ThreePrimeUTR | FBtr0076204-3-prime-utr | Drosophila melanogaster |
ThreePrimeUTR | FBtr0076205-3-prime-utr | Drosophila melanogaster |
Other
23 Pathways
- Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE,
- Disease,
- Defective GIF causes intrinsic factor deficiency,
- Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC,
- Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF,
- Metabolism,
- Metabolism of vitamins and cofactors,
- Molybdenum cofactor biosynthesis,
- Defective MMAB causes methylmalonic aciduria type cblB,
- Defective MMAA causes methylmalonic aciduria type cblA,
- Metabolism of water-soluble vitamins and cofactors,
- Defects in cobalamin (B12) metabolism,
- Defective CUBN causes hereditary megaloblastic anemia 1,
- Defective MTR causes methylmalonic aciduria and homocystinuria type cblG,
- Defective CD320 causes methylmalonic aciduria,
- Defective TCN2 causes hereditary megaloblastic anemia,
- Defects in biotin (Btn) metabolism,
- Defective AMN causes hereditary megaloblastic anemia 1,
- Defective HLCS causes multiple carboxylase deficiency,
- Defective BTD causes biotidinase deficiency,
- Defective MUT causes methylmalonic aciduria mut type,
- Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD,
- Defects in vitamin and cofactor metabolism
2 Cross References
Identifier |
Source . Name |
Subject . Primary Identifier |
---|---|---|
39238 | NCBI Entrez Gene identifiers | FBgn0263241 |
64613 | BioGRID | FBgn0263241 |
9 Data Sets
Name | URL |
---|---|
FlyBase data set for Drosophila melanogaster | |
Swiss-Prot data set | http://ca.expasy.org/sprot |
Drosophila 12 Genomes Consortium homology | |
GenomeRNAi data set | |
TreeFam data set | |
Panther data set | |
BioGRID interaction data set | http://www.thebiogrid.org/downloads.php |
GO Annotation from FlyBase | |
FlyBase fasta data set for Drosophila melanogaster |
5 Introns
5 RNAi Results
Screen | Gene | Phenotype | Score | Conditions | PubMed ID |
---|---|---|---|---|---|
Lipid storage | Mocs1 | none | 0.153565547 | 19067489 | |
Lipid storage | Mocs1 | none | 1.202489645 | 19067489 | |
Mitochondrial biogenesis and function | Mocs1 | Decreased mitochondrial citrate synthase activity | 0.723 | 18042644 | |
Hippo pathway regulation | Mocs1 | none | -0.3 | 23263283 | |
Glycosylation regulation (1) | Mocs1 | none | sp | 21203496 |