Ren1 Gene Summary [Mouse]

Enables aspartic-type endopeptidase activity. Involved in angiotensin maturation; male gonad development; and mesonephros development. Acts upstream of or within with a positive effect on regulation of blood pressure. Acts upstream of or within several processes, including drinking behavior; hormone-mediated signaling pathway; and renin-angiotensin regulation of aldosterone production. Located in extracellular space. Is active in extracellular region. Is expressed in several structures, including alimentary system; brain; extraembryonic component; genitourinary system; and trunk. Human ortholog(s) of this gene implicated in autosomal dominant tubulointerstitial kidney disease; essential hypertension; hand, foot and mouth disease; hypertension; and portal hypertension. Orthologous to human REN (renin). [provided by Alliance of Genome Resources, Apr 2025]

Details

Type
Protein Coding
Official Symbol
Ren1
Official Name
renin 1 structural [Source:MGI Symbol;Acc:MGI:97898]
Ensembl ID
ENSMUSG00000070645
Bio databases IDs NCBI: 19701 NCBI: 19702 Ensembl: ENSMUSG00000070645
Aliases renin 1 structural
Synonyms Ren, Ren-B, renin 2 tandem duplication of Ren1, Rn-2, Rnr
Species
Mouse, Mus musculus

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in mouse Ren1 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • Xylanase inhibitor N-terminal
  • endopeptidase
  • peptidase
  • aspartic endopeptidase
  • receptor binding
  • Cellular and retroviral pepsin-like aspartate proteases
  • Eukaryotic aspartyl protease
  • insulin-like growth factor receptor binding

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
regulates
regulated by
disease
  • hypertension
  • juvenile hyaline fibromatosis
  • diastolic dysfunction
  • reactive hypoglycemia
  • perivascular fibrosis
phenotypes
  • abnormal baroreceptor physiology
  • abnormal blood homeostasis
  • abnormal innervation
  • abnormal juxtaglomerular apparatus morphology
  • abnormal juxtaglomerular cell morphology
  • abnormal kidney afferent arteriole morphology
  • abnormal kidney cortex morphology
  • abnormal kidney interlobular artery morphology
  • abnormal kidney medulla morphology
  • abnormal locomotor behavior
  • abnormal macula densa morphology
  • abnormal renal glomerulus morphology
  • abnormal urine homeostasis
  • decreased body weight
  • decreased circulating renin level
  • decreased hematocrit
  • decreased kidney weight
  • decreased mean systemic arterial blood pressure
  • decreased physiological sensitivity to xenobiotic
  • decreased renal glomerular filtration rate
  • decreased systemic arterial blood pressure
  • decreased systemic arterial diastolic blood pressure
  • decreased systemic arterial systolic blood pressure
  • decreased urine osmolality
  • decreased vasoconstriction
  • dehydration
  • dilated renal tubules
  • glomerulosclerosis
  • granular kidney
  • hydronephrosis
  • hypotension
  • increased blood urea nitrogen level
  • increased circulating aldosterone level
  • increased circulating creatinine level
  • increased circulating potassium level
  • increased heart rate
  • kidney atrophy
  • kidney cortex atrophy
  • kidney inflammation
  • kidney medulla atrophy
  • kidney papillary atrophy
  • kidney papillary hypoplasia
  • metabolic acidosis
  • no abnormal phenotype detected
  • polydipsia
  • polyuria
  • postnatal lethality complete penetrance
  • postnatal lethality incomplete penetrance
  • proximal convoluted tubule brush border loss
  • renal glomerulus atrophy
  • renal glomerulus fibrosis
  • renal glomerulus hypertrophy
  • renal interstitial fibrosis
  • renal tubule atrophy
  • small kidney
  • vascular smooth muscle hyperplasia
role in cell
  • damage
  • loss
  • peroxidation in

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Extracellular Space
  • apical compartment

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.