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Protein : FBpp0070845 D. melanogaster

Primary Accession  ? Q8IRR1 Organism . Name  Drosophila melanogaster
MD5 Checksum  2506afdb1404582a995358ed354b3f35 UniProt Accession  Q8IRR1
UniProt Name  VNNL2_DROME GenBank Identifier  AAN09160
Is UniProt Canonical  true Is Fragment  false
Length  517 Molecular Weight  58716
Name  Vanin-like protein 2 Secondary Identifier  FBpp0070845

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1 Genes

DB identifier Secondary Identifier Symbol Name Source Organism
FBgn0052751 CG32751 CG32751 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
Dm.17661 UniGene FBpp0070845
NP_727068.1 RefSeq FBpp0070845

3 Data Sets

Name URL
FlyBase data set for Drosophila melanogaster  
Swiss-Prot data set
Reactome data set  

0 Ec Numbers

1 Locations

Located On . Primary Identifier
Start End Strand
X 6090760 6092651 -1

23 Pathways

Identifier Name
112201 Metabolism
165965 Biotin transport and 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

2 Protein Domains

DB identifier Name Short Name Type
IPR003010 Carbon-nitrogen hydrolase C-N_Hydrolase Domain
IPR012101 Biotinidase, eukaryotic Biotinidase_euk Family

1 Transcripts

DB identifier Gene
FBtr0070880 CG32751