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Protein : FBpp0085211 D. melanogaster

Primary Accession  ? Q9V9S9 Organism . Name  Drosophila melanogaster
MD5 Checksum  d2f3e0df76550c32ec394f8e60cf9311 UniProt Accession  Q9V9S9
UniProt Name  Q9V9S9_DROME GenBank Identifier  AAF57205
Is UniProt Canonical  true Is Fragment  false
Length  487 Molecular Weight  52493
Name  CG11576 Secondary Identifier  FBpp0085211

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0039882 CG11576 CG11576 FlyBase D. melanogaster


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


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2 Synonyms

0 Components

2 Cross References

Source . Name

Subject . Primary Identifier
NP_651901.3 RefSeq FBpp0085211
Dm.5916 UniGene FBpp0085211

3 Data Sets

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

0 Ec Numbers

1 Locations

Located On . Primary Identifier
Start End Strand
3R 27632841 27635463 -1

23 Pathways

Identifier Name
112201 Metabolism
84309 Vitamin B2 (riboflavin) metabolism
96904 Metabolism of vitamins and cofactors
99870 Metabolism of water-soluble vitamins and cofactors
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
118381 Disease

1 Protein Domains

DB identifier Name Short Name Type
IPR009357 Endogenous retrovirus receptor Endogenous_retrovirus_rcpt Family

1 Transcripts

DB identifier Gene
FBtr0085852 CG11576