CORIN - corin, serine peptidase Gene

Also Known as CRN; ATC2; Lrp4; PEE5; TMPRSS10

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10699

About CORIN

Cytogenetic location: 4p12 Genomic coordinates (GRCh38): 4:47,594,001-47,838,067 (from NCBI)

This gene has 11 transcripts (splice variants), 202 orthologues and is associated with 2 phenotypes. Biased expression in heart (RPKM 20.5), skin (RPKM 3.4) and 2 other tissues.

Summary

This gene encodes a member of the type II transmembrane serine protease class of the trypsin superfamily. Members of this family are composed of multiple structurally distinct domains. The encoded protein converts pro-atrial natriuretic peptide to biologically active atrial natriuretic peptide, a cardiac hormone that regulates blood volume and pressure. This protein may also function as a pro-brain-type natriuretic peptide convertase. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2013]

CORIN Products (3)

mRNA Protein Name
NM_001278585.2 NP_001265514.1 atrial natriuretic peptide-converting enzyme isoform 2
NM_001278586.2 NP_001265515.1 atrial natriuretic peptide-converting enzyme isoform 3
NM_006587.4 NP_006578.2 atrial natriuretic peptide-converting enzyme isoform 1
Molecular Function GO Annotation Evidence References Source
enables endopeptidase activity IMP
IMP: Inferred from mutant phenotype
20489134 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
32296183 GOA
enables serine-type endopeptidase activity IDA
IDA: Inferred from direct assay
10880574 GOA
Biological Process GO Annotation Evidence References Source
involved in female pregnancy IMP
IMP: Inferred from mutant phenotype
22437503 GOA
involved in peptide hormone processing IDA
IDA: Inferred from direct assay
10880574 GOA
involved in regulation of systemic arterial blood pressure by atrial natriuretic peptide IMP
IMP: Inferred from mutant phenotype
22437503 GOA
Cellular Component GO Annotation Evidence References Source
located in plasma membrane IDA
IDA: Inferred from direct assay
21518754 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CORIN Protein Structure

Fz

Fz: Fz domain (139 - 249)

Ldl_recept_a

Ldl_recept_a: Low-density lipoprotein receptor domain class A (272 - 304)

Ldl_recept_a

Ldl_recept_a: Low-density lipoprotein receptor domain class A (305 - 340)

Ldl_recept_a

Ldl_recept_a: Low-density lipoprotein receptor domain class A (342 - 377)

Ldl_recept_a

Ldl_recept_a: Low-density lipoprotein receptor domain class A (386 - 414)

Fz

Fz: Fz domain (455 - 570)

Ldl_recept_a

Ldl_recept_a: Low-density lipoprotein receptor domain class A (579 - 614)

Ldl_recept_a

Ldl_recept_a: Low-density lipoprotein receptor domain class A (655 - 689)

SRCR_2

SRCR_2: Scavenger receptor cysteine-rich domain (710 - 793)

Trypsin

Trypsin: Trypsin (802 - 1030)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1042 a.a.
Protein Preferred Names Protein Names

atrial natriuretic peptide-converting enzyme

  • heart-specific serine proteinase ATC2

CORIN Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CORIN Q9Y5Q5 GPX8 Homo sapiens Q8TED1 32296183
Intra
CORIN Q9Y5Q5 GPX8 Homo sapiens Q8TED1 32296183
Intra
CORIN Q9Y5Q5 AQP6 Homo sapiens Q13520 32296183
Intra
CORIN Q9Y5Q5 AQP6 Homo sapiens Q13520 32296183
Intra
CORIN Q9Y5Q5 CLDN5 Homo sapiens O00501 32296183
Intra
CORIN Q9Y5Q5 CLDN5 Homo sapiens O00501 32296183
Intra
CORIN Q9Y5Q5 EMP1 Homo sapiens P54849 32296183
Intra
CORIN Q9Y5Q5 EMP1 Homo sapiens P54849 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

CORIN Antibodies

Cat. No. Product Name Application Reactivity
HY-P89589 Corin Antibody (YA8933) WB, IP, ELISA human

Related Diseases

Diseases Alias
Preeclampsia/Eclampsia 5
  • PEE5

  • Pre-Eclampsia/Eclampsia 5

  • Gestational Proteinuric Hypertension

  • Preeclampsia/Eclampsia, Type 5

Pre-Eclampsia
  • Preeclampsia

  • Gestational Hypertension

  • Hypertension Induced By Pregnancy

  • Pre-Eclamptic Toxaemia

  • Pregnancy Associated Hypertension

  • Proteinuric Hypertension Of Pregnancy

  • Hypertension, Pregnancy-Induced, Susceptibility To

  • Preeclampsia/Eclampsia

  • Pregnancy Toxemia

  • Toxaemia Of Pregnancy

  • Gestational Proteinuric Hypertension

  • Pregnancy-Induced Hypertension

  • Toxemia Of Pregnancy

  • Preeclampsia, Susceptibility To

  • Transient Hypertension Of Pregnancy

  • Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria

  • Gestational Hypertension Nos

  • Mild Proteinuric Hypertension Of Pregnancy

  • Pih - [Pregnancy-Induced Hypertension]

  • Pregnancy-Induced Hypertension Nos

  • Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria

  • Pe - [Pre-Eclampsia]

  • Pre-Eclampsia Nos

  • Pre-Eclamptic Nos

  • Pregnancy Pre-Eclampsia

  • Puerperal Pre-Eclampsia

  • Pre-Eclampsia Toxaemia

  • Toxaemia In Pregnancy

  • Pet - [Pre-Eclamptic Toxaemia]

  • Maternal Toxaemia

Eclampsia
  • Eclampsia In Puerperium

  • Postpartum Eclampsia

  • Eclampsia, Postpartum

  • Puerperal Eclampsia

Cone-Rod Dystrophy 12
  • CORD12

  • Dystrophy, Cone-Rod, Type 12

St. Louis Encephalitis
  • Saint Louis Encephalitis

  • Neuroinvasive St. Louis Encephalitis Virus Infection

  • Encephalitis, St. Louis

  • Neuroinvasive Saint Louis Encephalitis Virus Infection

  • St. Louis Encephalitis Virus Infection

  • St. Louis Encephalitis Virus Neuroinvasive Disease

  • St. Louis Viral Disease

  • Type C Lethargic Encephalitis

  • Encephalitis Type C

Heart Disease
  • Heart Failure

  • Congenital Heart Disease

  • Heart Diseases

  • Congenital Heart Defects

  • Congenital Heart Defect

  • Heart Malformation

  • Congenital Anomaly Of Heart

  • Heart Defect

  • Heart-Congenital Defect

  • Congenital Heart Disorder

  • Heart Defects Congenital

  • Heart Defects, Congenital

  • Heart Defects

  • Heart Disease, Congenital

  • Disease, Heart, Congenital

  • Congestive Heart Failure

Hypertension, Essential
  • Essential Hypertension

  • Hypertension

  • High Blood Pressure

  • Hypertension, Essential, Susceptibility To

  • Hypertensive Disease

  • Primary Hypertension

  • EHT

  • Hypertension, Salt-Sensitive Essential, Susceptibility To

  • Hyperpiesia

  • Idiopathic Hypertension

  • Hypertensive Disorder

  • Hypertension, Essential, Susceptibility To, 3

  • Hypertension, Essential 3

  • Hypertension, Essential, Salt-Sensitive

  • Hypertension, Essential, Susceptibility To, 6

  • Hypertension, Essential 6

  • Hypertension, Salt-Sensitive Essential

  • Hypertension, Susceptibility To

  • Hypertension, Essential, Susceptibility To, 4

  • Hypertension, Essential 4

  • Hypertension, Essential, Susceptibility To, 2

  • Hypertension, Essential 2

  • Hypertension, Essential, Susceptibility To, 1

  • Hypertension, Essential 1

  • Hypertension, Essential, Susceptibility To, 5

  • Hypertension, Essential 5

  • Htn

  • Vascular Hypertensive Disorder

  • Systemic Primary Arterial Hypertension

  • Hbp - [High Blood Pressure]

  • Systemic Arterial Hypertensive Disorder

  • Elevated Blood Pressure

  • Arterial Hypertension Nos

  • Hypertension Nos

  • Benign Hypertension

  • Systemic Arterial Hypertension

  • Systemic Hypertension

  • Artery Htn

  • Benign Htn

  • Vascular Htn

  • Vascular Hypertension

  • Cholesterol Hypertension

  • Cholesterol Htn

  • Idiopathic Htn

  • Malignant Hypertension

  • Malignant Htn

  • Raised Blood Pressure

  • Cardiovascular Hypertension

  • Primary Htn - [Hypertension]

  • High Arterial Tension

  • High Blood Pressure Disorder

  • Ht - [Hypertension]

  • Htn - [Hypertension]

  • Hypertensive Vascular Disease

  • Hypertensive Vascular Degeneration

Dilated Cardiomyopathy
  • Familial Dilated Cardiomyopathy

  • Primary Dilated Cardiomyopathy

  • Idiopathic Dilated Cardiomyopathy

  • Congestive Cardiomyopathy

  • Idiopathic Dilation Cardiomyopathy

  • Primary Familial Dilated Cardiomyopathy

  • Cardiomyopathy, Dilated

  • DCM

  • Cardiomyopathy, Familial Dilated

  • Dilated Cardiomyopathy, Familial

  • Hypokinetic Dilated Cardiomyopathy, Familial

  • Familial Idiopathic Cardiomyopathy

  • Fdc

  • Cardiomyopathy, Familial Idiopathic

  • Idiopathic Cardiomegaly

  • Dilated Congestive Cardiomyopathy

  • Chronic Dilated Cardiomyopathy

  • Ccm - [Congestive Cardiomyopathy]

  • Cocm - [Congestive Cardiomyopathy]

  • Dcm - [Dilated Cardiomyopathy]

  • Dilated-Hypokinetic Cardiomyopathy

  • Congestive Idiopathic Cardiomyopathy

  • Primary Idiopathic Dilated Cardiomyopathy

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus CORIN VGNC VGNC:27619
Felis catus CORIN VGNC VGNC:78471
Macaca mulatta CORIN VGNC VGNC:71212
Canis familiaris CORIN VGNC VGNC:39526
Rattus norvegicus CORIN RGD RGD:727887
Mus musculus CORIN MGD MGI:1349451
Others CORIN NCBI