Target Gene Table
VIS IDVirusEnsembl IDGene TypeTarget GeneOncogeneTumor Suppressor GeneNCBI IDUniprot ID
TVIS10010545HBVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS10010546HBVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS10011227HBVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS10044642HBVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS10044643HBVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS10042159HBVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS10042160HBVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS10057422HBVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS30079620HIVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TVIS30081725HIVENSG00000153904.21protein_codingDDAH1NoNo23576B1AKK2
B4DYP1
O94760
TCGA Plot Options
Drug Information
GeneDDAH1
DrugBank IDDB00155
Drug NameCitrulline
Target IDBE0000766
UniProt IDO94760
Regulation Type
PubMed IDs14766200; 10950934; 12615801
CitationsMishima T, Hamada T, Ui-Tei K, Takahashi F, Miyata Y, Imaki J, Suzuki H, Yamashita K: Expression of DDAH1 in chick and rat embryos. Brain Res Dev Brain Res. 2004 Feb 20;148(2):223-32.@@Tran CT, Fox MF, Vallance P, Leiper JM: Chromosomal localization, gene structure, and expression pattern of DDAH1: comparison with DDAH2 and implications for evolutionary origins. Genomics. 2000 Aug 15;68(1):101-5.@@Arrigoni FI, Vallance P, Haworth SG, Leiper JM: Metabolism of asymmetric dimethylarginines is regulated in the lung developmentally and with pulmonary hypertension induced by hypobaric hypoxia. Circulation. 2003 Mar 4;107(8):1195-201.
GroupsInvestigational; Nutraceutical
Direct ClassificationL-alpha-amino acids
SMILESN[C@@H](CCCNC(N)=O)C(O)=O
PathwaysCitrullinemia Type I; Guanidinoacetate Methyltransferase Deficiency (GAMT Deficiency); Argininemia; Hyperornithinemia with Gyrate Atrophy (HOGA); Canavan Disease; Hypoacetylaspartia; Hyperprolinemia Type II; Argininosuccinic Aciduria; L-Arginine:Glycine Amidinotransferase Deficiency; Hyperornithinemia-Hyperammonemia-Homocitrullinuria [HHH-syndrome]; Arginine: Glycine Amidinotransferase Deficiency (AGAT Deficiency); Prolidase Deficiency (PD); Creatine Deficiency, Guanidinoacetate Methyltransferase Deficiency; Carbamoyl Phosphate Synthetase Deficiency; Ornithine Aminotransferase Deficiency (OAT Deficiency); Hyperprolinemia Type I; Aspartate Metabolism; Nitric Oxide Signaling Pathway; Arginine and Proline Metabolism; Ornithine Transcarbamylase Deficiency (OTC Deficiency); Prolinemia Type II; Urea Cycle
PharmGKBPA164747225
ChEMBLCHEMBL444814