BMP10 - bone morphogenetic protein 10 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 27302

About BMP10

Cytogenetic location: 2p13.3 Genomic coordinates (GRCh38): 2:68,860,909-68,871,397 (from NCBI)

This gene has 1 transcript (splice variant), 274 orthologues and 31 paralogues. Restricted expression toward heart (RPKM 211.3).

Summary

This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of Smad Family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate the mature protein, which binds to the activin receptor-like kinase 1 (ALK1) and plays important roles in cardiovascular development including cardiomyocyte proliferation and regulation of heart size, closure of the ductus arteriosus, angiogenesis and ventricular trabeculation. [provided by RefSeq, Aug 2016]

BMP10 Products (1)

mRNA Protein Name
NM_014482.3 NP_055297.1 bone morphogenetic protein 10 preproprotein
Molecular Function GO Annotation Evidence References Source
enables growth factor activity IDA
IDA: Inferred from direct assay
19903896 GOA
enables hormone activity IDA
IDA: Inferred from direct assay
17921333 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
17068149 GOA
enables receptor serine/threonine kinase binding IDA
IDA: Inferred from direct assay
17068149 GOA
enables telethonin binding IPI
IPI: Inferred from physical interaction
17921333 GOA
Biological Process GO Annotation Evidence References Source
acts upstream of or within BMP signaling pathway IDA
IDA: Inferred from direct assay
16049014 GOA
involved in BMP signaling pathway IDA
IDA: Inferred from direct assay
16049014 GOA
involved in activin receptor signaling pathway IDA
IDA: Inferred from direct assay
16049014 GOA
involved in negative regulation of cell growth IDA
IDA: Inferred from direct assay
17068149 GOA
involved in negative regulation of cell migration IDA
IDA: Inferred from direct assay
17068149 GOA
involved in negative regulation of endothelial cell migration IDA
IDA: Inferred from direct assay
17068149 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
16049014 GOA
involved in positive regulation of SMAD protein signal transduction IDA
IDA: Inferred from direct assay
16049014 GOA
involved in positive regulation of cardiac muscle hypertrophy IMP
IMP: Inferred from mutant phenotype
17921333 GOA
involved in positive regulation of sarcomere organization IDA
IDA: Inferred from direct assay
17921333 GOA
involved in regulation of cardiac muscle contraction IMP
IMP: Inferred from mutant phenotype
17921333 GOA
involved in regulation of cardiac muscle hypertrophy in response to stress IDA
IDA: Inferred from direct assay
17921333 GOA
Cellular Component GO Annotation Evidence References Source
located in Z disc IDA
IDA: Inferred from direct assay
17921333 GOA
located in cell surface IDA
IDA: Inferred from direct assay
17921333 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
17921333 GOA
located in extracellular space IDA
IDA: Inferred from direct assay
17921333 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

BMP10 Protein Structure

TGFb_propeptide

TGFb_propeptide: TGF-beta propeptide (49 - 256)

TGF_beta

TGF_beta: Transforming growth factor beta like domain (321 - 424)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 424 a.a.
Protein Preferred Names Protein Names

bone morphogenetic protein 10

BMP10 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
BMP10 O95393 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
BMP10 O95393 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
BMP10 O95393 JAGN1 Homo sapiens Q8N5M9 32296183
Intra
BMP10 O95393 CISD2 Homo sapiens Q8N5K1 32296183
Intra
BMP10 O95393 CISD2 Homo sapiens Q8N5K1 32296183
Intra
BMP10 O95393 CISD2 Homo sapiens Q8N5K1 32296183
Intra
BMP10 O95393 PLPP4 Homo sapiens Q5VZY2 32296183
Intra
BMP10 O95393 PLPP4 Homo sapiens Q5VZY2 32296183
Intra
BMP10 O95393 PLPP4 Homo sapiens Q5VZY2 32296183
Intra
BMP10 O95393 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
BMP10 O95393 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
BMP10 O95393 SPAG4 Homo sapiens Q9NPE6 32296183
Intra
BMP10 O95393 LRRC25 Homo sapiens Q8N386 32296183
Intra
BMP10 O95393 LRRC25 Homo sapiens Q8N386 32296183
Intra
BMP10 O95393 LRRC25 Homo sapiens Q8N386 32296183
Intra
BMP10 O95393 ARL13B Homo sapiens Q3SXY8 32296183
Intra
BMP10 O95393 ARL13B Homo sapiens Q3SXY8 32296183
Intra
BMP10 O95393 ARL13B Homo sapiens Q3SXY8 32296183
Intra
BMP10 O95393 BSCL2 Homo sapiens J3KQ12 32296183
Intra
BMP10 O95393 BSCL2 Homo sapiens J3KQ12 32296183
Intra
BMP10 O95393 GPX8 Homo sapiens Q8TED1 32296183
Intra
BMP10 O95393 GPX8 Homo sapiens Q8TED1 32296183
Intra
BMP10 O95393 GPX8 Homo sapiens Q8TED1 32296183
Intra
BMP10 O95393 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
BMP10 O95393 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
BMP10 O95393 FNDC9 Homo sapiens Q8TBE3 32296183
Intra
BMP10 O95393 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
BMP10 O95393 TMPRSS2 Homo sapiens O15393-2 32296183
Intra
BMP10 O95393 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
BMP10 O95393 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
BMP10 O95393 MS4A3 Homo sapiens Q96HJ5 32296183
Intra
BMP10 O95393 AQP6 Homo sapiens Q13520 32296183
Intra
BMP10 O95393 AQP6 Homo sapiens Q13520 32296183
Intra
BMP10 O95393 AQP6 Homo sapiens Q13520 32296183
Intra
BMP10 O95393 TNFSF8 Homo sapiens P32971 32296183
Intra
BMP10 O95393 TNFSF8 Homo sapiens P32971 32296183
Intra
BMP10 O95393 TNFSF8 Homo sapiens P32971 32296183
Intra
BMP10 O95393 GPR152 Homo sapiens Q8TDT2 32296183
Intra
BMP10 O95393 GPR152 Homo sapiens Q8TDT2 32296183
Intra
BMP10 O95393 GPR152 Homo sapiens Q8TDT2 32296183
Intra
BMP10 O95393 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
BMP10 O95393 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
BMP10 O95393 SLC35C2 Homo sapiens Q9NQQ7-3 32296183
Intra
BMP10 O95393 GJB1 Homo sapiens P08034 32296183
Intra
BMP10 O95393 GJB1 Homo sapiens P08034 32296183
Intra
BMP10 O95393 IL3RA Homo sapiens P26951 32296183
Intra
BMP10 O95393 IL3RA Homo sapiens P26951 32296183
Intra
BMP10 O95393 IL3RA Homo sapiens P26951 32296183
Intra
BMP10 O95393 TSPAN31 Homo sapiens Q12999 32296183
Intra
BMP10 O95393 TSPAN31 Homo sapiens Q12999 32296183
Intra
BMP10 O95393 TSPAN31 Homo sapiens Q12999 32296183
Intra
BMP10 O95393 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
BMP10 O95393 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
BMP10 O95393 SLC10A6 Homo sapiens Q3KNW5 32296183
Intra
BMP10 O95393 FAM209A Homo sapiens Q5JX71 32296183
Intra
BMP10 O95393 FAM209A Homo sapiens Q5JX71 32296183
Intra
BMP10 O95393 FAM209A Homo sapiens Q5JX71 32296183
Intra
BMP10 O95393 TMEM86B Homo sapiens Q8N661 32296183
Intra
BMP10 O95393 TMEM86B Homo sapiens Q8N661 32296183
Intra
BMP10 O95393 TMEM86B Homo sapiens Q8N661 32296183
Intra
BMP10 O95393 FFAR2 Homo sapiens O15552 32296183
Intra
BMP10 O95393 FFAR2 Homo sapiens O15552 32296183
Intra
BMP10 O95393 GGT6 Homo sapiens Q6P531 32296183
Intra
BMP10 O95393 GGT6 Homo sapiens Q6P531 32296183
Intra
BMP10 O95393 GGT6 Homo sapiens Q6P531 32296183
Intra
BMP10 O95393 FCGR1A Homo sapiens P12314 32296183
Intra
BMP10 O95393 FCGR1A Homo sapiens P12314 32296183
Intra
BMP10 O95393 FCGR1A Homo sapiens P12314 32296183
Intra
BMP10 O95393 CD33 Homo sapiens P20138 32296183
Intra
BMP10 O95393 CD33 Homo sapiens P20138 32296183
Intra
BMP10 O95393 CD33 Homo sapiens P20138 32296183
Intra
BMP10 O95393 KIR3DL1 Homo sapiens P43629 32296183
Intra
BMP10 O95393 KIR3DL1 Homo sapiens P43629 32296183
Intra
BMP10 O95393 KIR3DL1 Homo sapiens P43629 32296183
Intra
BMP10 O95393 EBP Homo sapiens Q15125 32296183
Intra
BMP10 O95393 EBP Homo sapiens Q15125 32296183
Intra
BMP10 O95393 EBP Homo sapiens Q15125 32296183
Intra
BMP10 O95393 FKBP7 Homo sapiens Q9Y680 32296183
Intra
BMP10 O95393 FKBP7 Homo sapiens Q9Y680 32296183
Intra
BMP10 O95393 FKBP7 Homo sapiens Q9Y680 32296183
Intra
BMP10 O95393 SLC10A1 Homo sapiens Q14973 32296183
Intra
BMP10 O95393 SLC10A1 Homo sapiens Q14973 32296183
Intra
BMP10 O95393 SLC10A1 Homo sapiens Q14973 32296183
Intra
BMP10 O95393 TMEM45B Homo sapiens Q96B21 32296183
Intra
BMP10 O95393 TMEM45B Homo sapiens Q96B21 32296183
Intra
BMP10 O95393 TMEM45B Homo sapiens Q96B21 32296183
Intra
BMP10 O95393 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
BMP10 O95393 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
BMP10 O95393 MTIF3 Homo sapiens Q9H2K0 32296183
Intra
BMP10 O95393 LRRC4C Homo sapiens Q9HCJ2 32296183
Intra
BMP10 O95393 LRRC4C Homo sapiens Q9HCJ2 32296183
Intra
BMP10 O95393 LRRC4C Homo sapiens Q9HCJ2 32296183
Intra
BMP10 O95393 APOA5 Homo sapiens Q6Q788 32296183
Intra
BMP10 O95393 APOA5 Homo sapiens Q6Q788 32296183
Intra
BMP10 O95393 APOA5 Homo sapiens Q6Q788 32296183
Intra
BMP10 O95393 FCRL4 Homo sapiens Q96PJ5 32296183
Intra
BMP10 O95393 FCRL4 Homo sapiens Q96PJ5 32296183
Intra
BMP10 O95393 FCRL4 Homo sapiens Q96PJ5 32296183
Intra
BMP10 O95393 TNFSF14 Homo sapiens O43557 32296183
Intra
BMP10 O95393 TNFSF14 Homo sapiens O43557 32296183
Intra
BMP10 O95393 TCTA Homo sapiens P57738 32296183
Intra
BMP10 O95393 TCTA Homo sapiens P57738 32296183
Intra
BMP10 O95393 TCTA Homo sapiens P57738 32296183
Intra
BMP10 O95393 CCDC70 Homo sapiens Q6NSX1 32296183
Intra
BMP10 O95393 CCDC70 Homo sapiens Q6NSX1 32296183
Intra
BMP10 O95393 CCDC70 Homo sapiens Q6NSX1 32296183
Intra
BMP10 O95393 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
BMP10 O95393 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
BMP10 O95393 CREB3L1 Homo sapiens Q96BA8 32296183
Intra
BMP10 O95393 SIT1 Homo sapiens Q9Y3P8 32296183
Intra
BMP10 O95393 SIT1 Homo sapiens Q9Y3P8 32296183
Intra
BMP10 O95393 SIT1 Homo sapiens Q9Y3P8 32296183
Intra
BMP10 O95393 BIK Homo sapiens Q13323 32296183
Intra
BMP10 O95393 BIK Homo sapiens Q13323 32296183
Intra
BMP10 O95393 BIK Homo sapiens Q13323 32296183
Intra
BMP10 O95393 DEXI Homo sapiens O95424 32296183
Intra
BMP10 O95393 DEXI Homo sapiens O95424 32296183
Intra
BMP10 O95393 DEXI Homo sapiens O95424 32296183
Intra
BMP10 O95393 COQ9 Homo sapiens O75208 32296183
Intra
BMP10 O95393 COQ9 Homo sapiens O75208 32296183
Intra
BMP10 O95393 MGST3 Homo sapiens O14880 32296183
Intra
BMP10 O95393 MGST3 Homo sapiens O14880 32296183
Intra
BMP10 O95393 CLDN7 Homo sapiens O95471 32296183
Intra
BMP10 O95393 CLDN7 Homo sapiens O95471 32296183
Intra
BMP10 O95393 CLDN7 Homo sapiens O95471 32296183
Intra
BMP10 O95393 VSIR Homo sapiens Q9H7M9 32296183
Intra
BMP10 O95393 VSIR Homo sapiens Q9H7M9 32296183
Intra
BMP10 O95393 VSIR Homo sapiens Q9H7M9 32296183
Intra
BMP10 O95393 MRPS18B Homo sapiens Q9Y676 32296183
Intra
BMP10 O95393 MRPS18B Homo sapiens Q9Y676 32296183
Intra
BMP10 O95393 MRPS18B Homo sapiens Q9Y676 32296183
Intra
BMP10 O95393 REEP4 Homo sapiens Q9H6H4 32296183
Intra
BMP10 O95393 REEP4 Homo sapiens Q9H6H4 32296183
Intra
BMP10 O95393 REEP4 Homo sapiens Q9H6H4 32296183
Intra
BMP10 O95393 SLC4A1 Homo sapiens P02730 32296183
Intra
BMP10 O95393 SLC4A1 Homo sapiens P02730 32296183
Intra
BMP10 O95393 SLC4A1 Homo sapiens P02730 32296183
Intra
BMP10 O95393 BSND Homo sapiens Q8WZ55 32296183
Intra
BMP10 O95393 BSND Homo sapiens Q8WZ55 32296183
Intra
BMP10 O95393 BSND Homo sapiens Q8WZ55 32296183
Intra
BMP10 O95393 KIR2DL3 Homo sapiens P43628 32296183
Intra
BMP10 O95393 KIR2DL3 Homo sapiens P43628 32296183
Intra
BMP10 O95393 KIR2DL3 Homo sapiens P43628 32296183
Intra
BMP10 O95393 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
BMP10 O95393 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
BMP10 O95393 TMEM14B Homo sapiens Q9NUH8 32296183
Intra
BMP10 O95393 KLRC1 Homo sapiens P26715 32296183
Intra
BMP10 O95393 KLRC1 Homo sapiens P26715 32296183
Intra
BMP10 O95393 KLRC1 Homo sapiens P26715 32296183
Intra
BMP10 O95393 ERP29 Homo sapiens P30040 32296183
Intra
BMP10 O95393 ERP29 Homo sapiens P30040 32296183
Intra
BMP10 O95393 ERP29 Homo sapiens P30040 32296183
Intra
BMP10 O95393 SLC38A1 Homo sapiens Q9H2H9 32296183
Intra
BMP10 O95393 SLC38A1 Homo sapiens Q9H2H9 32296183
Intra
BMP10 O95393 SLC38A1 Homo sapiens Q9H2H9 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant BMP10 Proteins

Cat. No. Product Name Accession Purity
HY-P700019AF Animal-Free BMP-10 Protein, Human (His) O95393 (N317-R424) ≥ 95%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
Myostatin-Related Muscle Hypertrophy
  • Mslhp

  • Muscle Hypertrophy Syndrome

Juvenile Polyposis/Hereditary Hemorrhagic Telangiectasia Syndrome
  • Juvenile Polyposis-Hereditary Hemorrhagic Telangiectasia Syndrome

  • JPHT

  • Jp/Hht Syndrome

  • Juvenile Polyposis With Hereditary Hemorrhagic Telangiectasia

  • Jps/Hht

  • Telangiectasia, Hereditary Hemorrhagic, With Juvenile Polyposis Coli

  • Polyposis, Generalized Juvenile, With Pulmonary Arteriovenous Malformation

  • Jp-Hht

  • JP/HHT

  • Polyposis, Juvenile/Hereditary Hemorrhagic Telangiectasia Syndrome

Pulmonary Hypertension
  • Primary Pulmonary Hypertension

  • Hypertension Pulmonary

  • Hypertension, Pulmonary

  • Hypertension, Pulmonary, Primary

  • Idiopathic Pulmonary Hypertension

  • Idiopathic Pulmonary Arterial Hypertension

  • Pulmonary Htn - [Hypertension]

Arteriovenous Malformation
  • Arteriovenous Malformations

  • Arteriovenous Hemangioma

  • Cirsoid Aneurysm

  • Racemose Aneurysm

  • Racemose Angioma

  • Racemose Hemangioma

  • Congenital Arteriovenous Malformation

Right Atrial Isomerism
  • Ivemark Syndrome

  • Asplenia With Cardiovascular Anomalies

  • RAI

  • Asplenia Syndrome

  • Asplenia

  • Right Isomerism

  • Splenic Agenesis Syndrome

  • Bilateral Right-Sidedness Sequence

  • Right Sided Atrial Isomerism

  • Isomerism Of Right Atrial Appendage

  • Heterotaxy, Visceroatrial, Autosomal Recessive

  • Polyasplenia

  • Vah, Autosomal Recessive

  • Atrial Isomerism, Right

  • Congenital Absence Of Spleen

  • Bilateral Right-Sidedness

Telangiectasis
  • Telangiectasia

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Acromesomelic Dysplasia 2a
  • Chondrodysplasia, Grebe Type

  • Acromesomelic Dysplasia, Grebe Type

  • Grebe Chondrodysplasia

  • Amdg

  • Grebe Syndrome

  • AMD2A

  • Grebe Dysplasia

  • Achondrogenesis, Brazilian

  • Achondrogenesis, Type Ii, Formerly

  • Acromesomelic Dysplasia-2a

  • Achondrogenesis Type Ii

  • Brazilian Achondrogenesis

  • Acromesomelic Chondrodysplasia, Grebe Type

Hereditary Hemorrhagic Telangiectasia
  • Rendu-Osler-Weber Disease

  • Hht

  • Osler-Weber-Rendu Disease

  • Telangiectasia, Hereditary Hemorrhagic

  • Osler Hemorrhagic Telangiectasia Syndrome

  • Orw Disease

  • Osler Weber Rendu Syndrome

  • Osler-Rendu-Weber Disease

  • Osler-Weber-Rendu Syndrome

  • Rendu-Osler Disease

  • Telangiectasia Hereditary Hemorrhagic

  • Telangiectasia Hemorrhagic, Hereditary

  • Hht - [Hereditary Haemorrhagic Telangiectasia]

  • Osler Haemorrhagic Telangiectasia Syndrome

Double Outlet Right Ventricle
  • Double Outlet Right Ventricle With Subpulmonary Ventricular Septal Defect

  • Taussig-Bing Syndrome

  • Dextrotransposition Of Aorta

  • Taussig-Bing Syndrome Or Defect

  • Dorv

  • Dorv With Subpulmonary Vsd

  • Dorv-Tga

  • Double Outlet Right Ventricle With Transposition Of The Great Arteries

  • Double Outlet Right Ventricle With Subpulmonary Interventricular Communication, Transposition Type

  • Taussig-Bing Heart

  • Taussig-Bing Malformation

  • Taussig-Bing Complex

  • Taussig-Bing Defect

  • Taussig-Bing

  • Double Outlet Right Ventricle With Remote Ventricular Septal Defect

  • Double Outlet Right Ventricle With Uncommitted Ventricular Septal Defect

  • Double Outlet Right Ventricle With Non-Committed Interventricular Communication

  • Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication Without Pulmonary Stenosis

  • Double Outlet Right Ventricle With Subaortic Or Doubly Committed Interventricular Communication And Pulmonary Stenosis

Heart Septal Defect
  • Septal Defect

  • Heart Septal Defects

  • Cardiac Septal Defects

  • Congenital Septal Defect Of Heart

Atrioventricular Septal Defect
  • AVSD

  • Atrioventricular Canal Defect

  • Avcd

  • Endocardial Cushion Defect

  • Ecd

  • Avc Defect

  • Atrioventricular Septal Defect, Susceptibility To, 1

  • Atrioventricular Septal Defect 1

  • Endocardial Cushion Defects

  • Septal Defect, Atrioventricular

  • Atrioventricular Defect With Atrial Shunting Only

  • Incomplete Atrioventricular Septal Defect With Isolated Atrial Component

  • Incomplete Atrioventricular Canal Defect With Isolated Atrial Component

  • Primum Atrial Septal Defect

  • Partial Atrioventricular Canal Defect With Isolated Atrial Component

  • Partial Atrioventricular Septal Defect, Ostium Primum Type

  • Ostium Primum Atrial Septal Defect

  • Partial Atrioventricular Canal Defect

  • Partial Atrioventricular Septal Defect

  • Atrial Septum Primum Defect

  • Atrioventricular Canal Defect With Isolated Ventricular Component

  • Atrioventricular Canal Defect With Isolated Ventricular Communication

  • Atrioventricular Septal Defect With Isolated Ventricular Component

  • Atrioventricular Septal Defect With Atrial Shunting And Restrictive Ventricular Shunting

  • Intermediate Atrioventricular Canal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valve

  • Transitional Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valves

  • Atrioventricular Canal Defect Associated With A Restrictive Ventricular Septal Defect

  • Intermediate Atrioventricular Canal Defect

  • Intermediate Atrioventricular Septal Defect With Atrial And Ventricular Components And Separate Atrioventricular Valvar Orifices

  • Intermediate Atrioventricular Septal Defect

  • Transitional Atrioventricular Canal Defect

  • Transitional Atrioventricular Septal Defect

  • Complete Atrioventricular Canal With Atrial And Ventricular Components

  • Complete Atrioventricular Canal Defect

  • Complete Atrioventricular Septal Defect

Ventricular Septal Defect
  • Ventricular Septal Defects

  • Interventricular Septal Defect

  • Heart Septal Defects, Ventricular

  • Ventricular Septal Abnormality

  • Interventricular Septum Defect

  • Ventricular Septum Defect

  • Vsd - [Ventricular Septum Defect]

  • Congenital Ventricular Septal Defect

  • Single Ventricular Septal Defect

Left Ventricular Noncompaction
  • Noncompaction Cardiomyopathy

  • Left Ventricular Hypertrabeculation

  • Lvnc

  • Spongy Myocardium

  • Isolated Noncompaction Of The Ventricular Myocardium

  • Left Ventricular Myocardial Noncompaction Cardiomyopathy

  • Fetal Myocardium

  • Honeycomb Myocardium

  • Hypertrabeculation Syndrome

  • Left Ventricular Non-Compaction

  • Lvht

  • Non-Compaction Of The Left Ventricular Myocardium

  • Ventricular Noncompaction, Left

  • Non-Compaction Cardiomyopathy

Aortic Valve Disease 1
  • Aortic Valve Disease

  • Bicuspid Aortic Valve

  • Aortic Valve Disorder

  • AOVD1

  • Bav

  • Bicuspid Aortic Valve Disease

  • Familial Bicuspid Aortic Valve

  • Aortic Valve Calcification

  • Aovd

  • Aortic Valve, Bicuspid

  • Aortic Valve, Calcification Of

  • Aortic Stenosis, Calcific

  • Familial Bav

  • Calcific Aortic Stenosis

  • Calcification Of Aortic Valve

  • Abnormality Of The Aortic Valve

  • Aortic Valve Disease, Type 1

  • Aortic Valve Disease 2

  • Bicommissural Aortic Valve

Atrial Heart Septal Defect
  • Atrial Septal Defect

  • Atrial Septal Defects

  • Atrioseptal Defect

  • Auricular Septal Defect

  • Congenital Atrial Septal Defect

  • Interatrial Septal Defect

  • Interauricular Septal Defect

  • Heart Septal Defects, Atrial

  • Septal Defect, Atrial

Tetralogy Of Fallot
  • TOF

  • Fallot Tetralogy

  • Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle

  • Tetrad Of Fallot

  • Fallot Tetrad

  • Fallot Disease

  • Fallot Complex

  • Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy

  • Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle

  • Interventricular Septal Defect, In Tetralogy Of Fallot

  • Ventricular Septal Defect With Obstructed Right Ventricular Outflow

  • Tof - [Tetralogy Of Fallot]

  • Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]

  • Pulmonary Atresia, Ventricular Septal Defect And Mapcas

  • Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]

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
Rattus norvegicus BMP10 RGD RGD:1562986
Mus musculus BMP10 MGD MGI:1338820
Bos taurus BMP10 VGNC VGNC:26515
Canis familiaris BMP10 VGNC VGNC:38476
Macaca mulatta BMP10 VGNC VGNC:70354
Others BMP10 NCBI