Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
183
Gene name Gene Name - the full gene name approved by the HGNC.
Angiotensinogen
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
AGT
Synonyms (NCBI Gene) Gene synonyms aliases
ANHU, SERPINA8, hFLT1
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1q42.2
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene, pre-angiotensinogen or angiotensinogen precursor, is expressed in the liver and is cleaved by the enzyme renin in response to lowered blood pressure. The resulting product, angiotensin I, is then cleaved by angiotensin co
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs699 A>G Benign, risk-factor Coding sequence variant, missense variant
rs74315283 C>A,T Pathogenic Missense variant, coding sequence variant
rs121912702 G>A Pathogenic Stop gained, coding sequence variant
rs387906578 A>-,AA Pathogenic Coding sequence variant, frameshift variant, stop gained
rs747815674 C>A Pathogenic Splice donor variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT028917 hsa-miR-26b-5p Microarray 19088304
MIRT2168949 hsa-miR-3613-3p CLIP-seq
MIRT2168950 hsa-miR-4457 CLIP-seq
MIRT2168951 hsa-miR-513b CLIP-seq
MIRT2168952 hsa-miR-548c-3p CLIP-seq
Transcription factors
Transcription factor Regulation Reference
NFKB1 Unknown 10628750;8613256
RELA Unknown 10628750;8613256
SP1 Unknown 12032593
USF1 Repression 18802024
YBX1 Activation 11829142
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001558 Process Regulation of cell growth NAS 17159080
GO:0001819 Process Positive regulation of cytokine production IDA 17906677
GO:0001822 Process Kidney development IMP 16116425
GO:0001974 Process Blood vessel remodeling TAS 10406457
GO:0002016 Process Regulation of blood volume by renin-angiotensin NAS 17159080
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
106150 333 ENSG00000135744
Protein
UniProt ID P01019
Protein name Angiotensinogen (Serpin A8) [Cleaved into: Angiotensin-1 (Angiotensin 1-10) (Angiotensin I) (Ang I); Angiotensin-2 (Angiotensin 1-8) (Angiotensin II) (Ang II); Angiotensin-3 (Angiotensin 2-8) (Angiotensin III) (Ang III) (Des-Asp[1]-angiotensin II); Angiot
Protein function Essential component of the renin-angiotensin system (RAS), a potent regulator of blood pressure, body fluid and electrolyte homeostasis. ; [Angioten
PDB 1N9U , 1N9V , 2JP8 , 2WXW , 2X0B , 3CK0 , 3WOO , 3WOR , 4AA1 , 4APH , 4FYS , 5E2Q , 5M3X , 5M3Y , 5XJM , 6I3F , 6I3I , 6JOD , 6OS0 , 7C6A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00079 Serpin 108 481 Serpin (serine protease inhibitor) Domain
Tissue specificity TISSUE SPECIFICITY: Expressed by the liver and secreted in plasma. {ECO:0000269|PubMed:1692023}.
Sequence
Sequence length 485
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Disease merge term Disease name dbSNP ID References
Renal Tubular Dysgenesis Of Genetic Origin Renal tubular dysgenesis, renal tubular dysgenesis of genetic origin rs74315283, rs121912702, rs387906578, rs747815674 N/A
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Coronary artery disease Coronary artery disease N/A N/A GWAS
Hypertension Essential hypertension (PheCode 401.1), High blood pressure / hypertension, Hypertension, Hypertension (confirmatory factor analysis Factor 12), Hypertension (PheCode 401) N/A N/A GWAS
Microcephaly microcephaly N/A N/A ClinVar
Pancreatic adenocarcinoma Pancreatic ductal adenocarcinoma N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Achalasia Addisonianism Alacrimia syndrome Associate 20945963
Acute Coronary Syndrome Associate 20549134
Acute Kidney Injury Associate 12911556, 24009222, 31880583
Albuminuria Associate 31611175
Alzheimer Disease Associate 27884212, 29348391
Amyotrophic Lateral Sclerosis Associate 27814735
Anemia Sickle Cell Associate 11754397
Aneurysm Associate 37731512
Aneurysm Ascending Aorta Stimulate 26071572
Angina Stable Associate 11451295