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Protein : FBpp0085319 D. melanogaster

Primary Accession  ? Q0IGX4 Organism . Name  Drosophila melanogaster
MD5 Checksum  cce8f0e2525a6135f0f288bafe588f95 UniProt Accession  Q0IGX4
UniProt Name  Q0IGX4_DROME GenBank Identifier  AAF57300
Is UniProt Canonical  true Is Fragment  false
Length  516 Molecular Weight  56786
Name  IP16073p Secondary Identifier  FBpp0085319

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0033047 CG7882 CG7882 FlyBase D. melanogaster


Protein --> Gene + chromosomal location and length of the gene.


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0 Components

3 Cross References

Source . Name

Subject . Primary Identifier
Dm.17874 UniGene FBpp0085319
NP_610189.2 RefSeq FBpp0085319
NP_724438.1 RefSeq FBpp0085319

3 Data Sets

Name URL
FlyBase data set for Drosophila melanogaster  
TrEMBL data set
Reactome data set  

0 Ec Numbers

2 Locations

Located On . Primary Identifier
Start End Strand
2R 1845378 1847222 1
2R 1845378 1847222 1

37 Pathways

Identifier Name
87602 Regulation of Insulin Secretion
89538 Integration of energy metabolism
106046 Carbohydrate metabolism
112201 Metabolism
96904 Metabolism of vitamins and cofactors
99870 Metabolism of water-soluble vitamins and cofactors
108418 Vitamin C (ascorbate) metabolism
113552 Developmental Biology
172141 Defective HLCS causes multiple carboxylase deficiency
170704 Defective BTD causes biotidinase deficiency
170877 Defective MMAA causes methylmalonic aciduria type cblA
171816 Defective MUT causes methylmalonic aciduria mut type
170863 Defective CD320 causes methylmalonic aciduria
170480 Defects in biotin (Btn) metabolism
170427 Defective MTRR causes methylmalonic aciduria and homocystinuria type cblE
170479 Defective MTR causes methylmalonic aciduria and homocystinuria type cblG
170421 Defective MMAB causes methylmalonic aciduria type cblB
172030 Defective MMACHC causes methylmalonic aciduria and homocystinuria type cblC
172052 Defective MMADHC causes methylmalonic aciduria and homocystinuria type cblD
172351 Defective LMBRD1 causes methylmalonic aciduria and homocystinuria type cblF
171186 Defective GIF causes intrinsic factor deficiency
172253 Defective CUBN causes hereditary megaloblastic anemia 1
172121 Defective TCN2 causes hereditary megaloblastic anemia
172488 Defects in cobalamin (B12) metabolism
172146 Defective AMN causes hereditary megaloblastic anemia 1
170642 Defects in vitamin and cofactor metabolism
93479 Regulation of beta-cell development
97083 Regulation of gene expression in beta cells
84551 Transcriptional Regulation of White Adipocyte Differentiation
118381 Disease

4 Protein Domains

DB identifier Name Short Name Type
IPR020846 Major facilitator superfamily domain MFS_dom Domain
IPR016196 Major facilitator superfamily domain, general substrate transporter MFS_dom_general_subst_transpt Domain
IPR005828 General substrate transporter Sub_transporter Family
IPR003663 Sugar/inositol transporter Sugar/inositol_transpt Family

2 Transcripts

DB identifier Gene
FBtr0085966 CG7882
FBtr0335266 CG7882