InnateDB Protein
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IDBP-106026.6
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Last Modified
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2014-10-13 [Report errors or provide feedback]
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Gene Symbol
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REN
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Protein Name
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renin
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Synonyms
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HNFJ2;
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Species
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Homo sapiens
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Ensembl Protein
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ENSP00000272190
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InnateDB Gene
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IDBG-106022 (REN)
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Protein Structure
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Function |
Renin is a highly specific endopeptidase, whose only known function is to generate angiotensin I from angiotensinogen in the plasma, initiating a cascade of reactions that produce an elevation of blood pressure and increased sodium retention by the kidney.
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Subcellular Localization |
Secreted. Membrane. Note=Associated to membranes via binding to ATP6AP2.
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Disease Associations |
Renal tubular dysgenesis (RTD) [MIM:267430]: Autosomal recessive severe disorder of renal tubular development characterized by persistent fetal anuria and perinatal death, probably due to pulmonary hypoplasia from early-onset oligohydramnios (the Potter phenotype). {ECO:0000269PubMed:16116425}. Note=The disease is caused by mutations affecting the gene represented in this entry.Familial juvenile hyperuricemic nephropathy 2 (HNFJ2) [MIM:613092]: A renal disease characterized by juvenile onset of hyperuricemia, slowly progressive renal failure and anemia. {ECO:0000269PubMed:19664745}. Note=The disease is caused by mutations affecting the gene represented in this entry.
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Tissue Specificity |
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Comments |
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Number of Interactions
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This gene and/or its encoded proteins are associated with 8 experimentally validated interaction(s) in this database.
Experimentally validated |
Total |
8
[view]
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Protein-Protein |
8
[view]
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Protein-DNA |
0
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Protein-RNA |
0
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DNA-DNA |
0
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RNA-RNA |
0
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DNA-RNA |
0
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Molecular Function |
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Biological Process |
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Cellular Component |
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PDB ID |
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InterPro |
IPR001461
Aspartic peptidase
IPR012848
Aspartic peptidase, N-terminal
IPR021109
Aspartic peptidase domain
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PFAM |
PF00026
PF07966
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PRINTS |
PR00792
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PIRSF |
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SMART |
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TIGRFAMs |
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Modification |
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SwissProt |
P00797
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PhosphoSite |
PhosphoSite-P00797
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TrEMBL |
Q9UQK5
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UniProt Splice Variant |
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Entrez Gene |
5972
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UniGene |
Hs.3210
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RefSeq |
NP_000528
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HUGO |
HGNC:9958
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OMIM |
179820
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CCDS |
CCDS30981
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HPRD |
01564
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IMGT |
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EMBL |
AF117822
AL592114
AL592146
AY436324
BC033474
BC047752
CR536498
EU332871
L00064
L00065
L00066
L00067
L00068
L00069
L00070
L00071
L00072
L00073
M10030
M10128
M10150
M10151
M10152
M13253
M15410
M26440
M26899
M26900
M26901
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GenPept |
AAA60262
AAA60263
AAA60363
AAA60364
AAA60365
AAD03461
AAD26254
AAH33474
AAH47752
AAR03502
ABY87560
CAG38737
CAH71224
CAI16594
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