Gene Gene information from NCBI Gene database.
Entrez ID 283
Gene name Angiogenin
Gene symbol ANG
Synonyms (NCBI Gene)
ALS9HEL168RAA1RNASE4RNASE5
Chromosome 14
Chromosome location 14q11.2
Summary The protein encoded by this gene is a member of the RNase A superfamily though it has relatively weak ribonucleolytic activity. This protein is a potent mediator of new blood vessel formation and thus, in addition to the name RNase5, is commonly called an
miRNA miRNA information provided by mirtarbase database.
86
miRTarBase ID miRNA Experiments Reference
MIRT006649 hsa-miR-409-3p ImmunofluorescenceImmunohistochemistryLuciferase reporter assayqRT-PCRWestern blot 22531314
MIRT018344 hsa-miR-335-5p Microarray 18185580
MIRT024617 hsa-miR-215-5p Microarray 19074876
MIRT026610 hsa-miR-192-5p Microarray 19074876
MIRT517273 hsa-miR-5580-3p HITS-CLIP 21572407
Transcription factors Transcription factors information provided by TRRUST V2 database.
2
Transcription factor Regulation Reference
CTCF Unknown 24659782
PPARD Repression 17511960
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
91
GO ID Ontology Definition Evidence Reference
GO:0001525 Process Angiogenesis IBA
GO:0001525 Process Angiogenesis IDA 8448182
GO:0001525 Process Angiogenesis IDA 3470787, 4074709
GO:0001525 Process Angiogenesis IEA
GO:0001525 Process Angiogenesis IMP 2479414, 17125737
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
105850 483 ENSG00000214274
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P03950
Protein name Angiogenin (EC 3.1.27.-) (Ribonuclease 5) (RNase 5)
Protein function Secreted ribonuclease that can either promote or restrict cell proliferation of target cells, depending on the context (PubMed:12051708, PubMed:1400510, PubMed:19332886, PubMed:20129916, PubMed:21855800, PubMed:23047679, PubMed:23843625, PubMed:
PDB 1A4Y , 1ANG , 1AWZ , 1B1E , 1B1I , 1B1J , 1GV7 , 1H0D , 1H52 , 1H53 , 1HBY , 1K58 , 1K59 , 1K5A , 1K5B , 1UN3 , 1UN4 , 1UN5 , 2ANG , 4AHD , 4AHE , 4AHF , 4AHG , 4AHH , 4AHI , 4AHJ , 4AHK , 4AHL , 4AHM , 4AHN , 4AOH , 4B36 , 5EOP , 5EPZ , 5EQO , 5M9A , 5M9C , 5M9G , 5M9J , 5M9M , 5M9P , 5M9Q , 5M9R , 5M9S , 5M9T , 5M9V , 7NPM , 7PNJ , 7PNP , 7PNR , 8AF0
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00074 RnaseA 28 140 Pancreatic ribonuclease Domain
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in the liver (PubMed:2440105). Also detected in endothelial cells and spinal cord neurons (PubMed:17886298, PubMed:2440105). {ECO:0000269|PubMed:17886298, ECO:0000269|PubMed:2440105}.
Sequence
Sequence length 147
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Amyotrophic lateral sclerosis   Adherens junctions interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
58
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Amyotrophic lateral sclerosis type 9 Pathogenic; Likely pathogenic rs121909535, rs121909537, rs121909538, rs121909539, rs121909540, rs121909542, rs121909544 RCV000019699
RCV000019701
RCV000019702
RCV000019703
RCV000019704
RCV000019706
RCV000019708
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Amyotrophic lateral sclerosis Uncertain significance rs1886957607 RCV001095486
Amyotrophic lateral sclerosis type 10 Conflicting classifications of pathogenicity rs201068740 RCV002463771
ANG-related disorder Uncertain significance; Likely benign; Conflicting classifications of pathogenicity; Benign rs535311762, rs141398857, rs2502151829, rs121909536, rs121909541, rs17560, rs149672657, rs201068740 RCV003401757
RCV003422511
RCV003894127
RCV003959800
RCV003934843
RCV003974847
RCV003940211
RCV003413776
RCV003413785
Frontotemporal dementia Uncertain significance rs535311762 RCV001848613
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Alzheimer Disease Stimulate 33337366
Amyopathic dermatomyositis Associate 23229115
Amyotrophic Lateral Sclerosis Associate 17886298, 19363631, 19449021, 20577002, 21085671, 22384259, 22752089, 23100398, 23228179, 23393617, 23665167, 23755159, 23881933, 25372031, 25386690
View all (8 more)
Amyotrophic lateral sclerosis 1 Associate 20577002, 23228179, 25386690
Astrocytoma Associate 25659096
Autoimmune Diseases Associate 24860242
Breast Neoplasms Associate 23977052, 24457100
Carcinogenesis Associate 11579593, 27317771
Carcinoma Hepatocellular Associate 14600132, 29614505, 33228611
Carcinoma Non Small Cell Lung Associate 40007122