1. Gene
  2. BMP7 - bone morphogenetic protein 7 Gene

BMP7 - bone morphogenetic protein 7 Gene

中文名称:骨形态发生蛋白 7

种属: Homo sapiens

同用名: OP-1

基因 ID: 655 | 基因类型: protein coding

关于 BMP7

Cytogenetic location: 20q13.31 Genomic coordinates (GRCh38): 20:57,168,753-57,266,641 (from NCBI)

This gene has 9 transcripts (splice variants), 270 orthologues and 31 paralogues. Biased expression in thyroid (RPKM 30.0), placenta (RPKM 15.8) and 9 other tissues.

功能概要

该基因编码 TGF-β (转化生长因子-β) 蛋白质超家族的分泌配体。该家族的配体结合各种 TGF-β 受体,导致调节基因表达的 SMAD 家族转录因子的募集和激活。编码的前原蛋白经过蛋白水解处理,生成二硫键连接的同源二聚体的每个亚基,在骨骼、肾脏和棕色脂肪组织的发育中发挥作用。此外,这种蛋白质可诱导异位骨形成,并可促进人类患者的骨折愈合。[RefSeq 提供,2016 年 7 月]

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 each subunit of the disulfide-linked homodimer, which plays a role in bone, kidney and brown adipose tissue development. Additionally, this protein induces ectopic bone formation and may promote fracture healing in human patients. [provided by RefSeq, Jul 2016]

BMP7 基因产物(1)

mRNA Protein Name
NM_001719.3 NP_001710.1 bone morphogenetic protein 7 preproprotein
基因本体论
  • 分子功能
  • 生物过程
  • 细胞组分
分子功能 GO 注释 逻辑证据 参考文献 来源
enables BMP receptor binding IPI
IPI: 通过物理相互作用推断
18184661 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
9872992 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in BMP signaling pathway IDA
IDA: 通过直接分析推断
16049014 GOA
involved in BMP signaling pathway IMP
IMP: 通过突变表型推断
18326817 GOA
involved in cellular response to BMP stimulus IMP
IMP: 通过突变表型推断
18326817 GOA
involved in mesenchymal cell differentiation IDA
IDA: 通过直接分析推断
9693150 GOA
involved in mesonephros development IEP
IEP: 通过表达模式推断
18437684 GOA
involved in metanephros development IEP
IEP: 通过表达模式推断
18437684 GOA
involved in monocyte aggregation IDA
IDA: 通过直接分析推断
15100360 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: 通过直接分析推断
15100360 GOA
involved in negative regulation of cell cycle IDA
IDA: 通过直接分析推断
11502704 GOA
involved in negative regulation of glomerular mesangial cell proliferation IDA
IDA: 通过直接分析推断
17244894 GOA
involved in negative regulation of mitotic nuclear division IDA
IDA: 通过直接分析推断
17244894 GOA
acts upstream of or within negative regulation of neuron differentiation IDA
IDA: 通过直接分析推断
16325379 GOA
acts upstream of or within neuron projection morphogenesis IDA
IDA: 通过直接分析推断
16325379 GOA
involved in positive regulation of DNA-templated transcription IDA
IDA: 通过直接分析推断
14517293 GOA
involved in positive regulation of DNA-templated transcription IMP
IMP: 通过突变表型推断
27923061 GOA
involved in positive regulation of SMAD protein signal transduction IDA
IDA: 通过直接分析推断
9311995 GOA
involved in positive regulation of bone mineralization IDA
IDA: 通过直接分析推断
18436533 GOA
involved in positive regulation of brown fat cell differentiation IMP
IMP: 通过突变表型推断
27923061 GOA
involved in positive regulation of dendrite development IDA
IDA: 通过直接分析推断
11580864 GOA
involved in positive regulation of gene expression IDA
IDA: 通过直接分析推断
28124060 GOA
involved in positive regulation of heterotypic cell-cell adhesion IDA
IDA: 通过直接分析推断
15100360 GOA
involved in positive regulation of hyaluranon cable assembly IDA
IDA: 通过直接分析推断
15100360 GOA
involved in positive regulation of osteoblast differentiation IDA
IDA: 通过直接分析推断
18436533 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in extracellular space IDA
IDA: 通过直接分析推断
17977014 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

BMP7 蛋白结构

TGFb_propeptide

TGFb_propeptide: TGF-beta propeptide (34 - 280)

TGF_beta

TGF_beta: Transforming growth factor beta like domain (328 - 431)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 431 a.a.
蛋白主名 其他名称

bone morphogenetic protein 7

osteogenic protein 1

BMP7 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
BMP7 P18075 KRTAP10-8 Homo sapiens P60410
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 KRTAP10-8 Homo sapiens P60410
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP10-8 Homo sapiens P60410
Validated Y2H
32296183
种属内
BMP7 P18075 KRTAP10-9 Homo sapiens P60411
Validated Y2H
32296183
种属内
BMP7 P18075 KRTAP10-9 Homo sapiens P60411
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP10-9 Homo sapiens P60411
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 KRTAP1-3 Homo sapiens Q8IUG1
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 KRTAP1-3 Homo sapiens Q8IUG1
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP12-3 Homo sapiens P60328
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 KRTAP12-3 Homo sapiens P60328
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP12-3 Homo sapiens P60328
Validated Y2H
32296183
种属内
BMP7 P18075 KRTAP9-8 Homo sapiens Q9BYQ0
Validated Y2H
32296183
种属内
BMP7 P18075 KRTAP9-8 Homo sapiens Q9BYQ0
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP9-8 Homo sapiens Q9BYQ0
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 CCDC125 Homo sapiens Q86Z20
Validated Y2H
32296183
种属内
BMP7 P18075 CCDC125 Homo sapiens Q86Z20
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 CCDC125 Homo sapiens Q86Z20
Y2H Array
32296183
种属内
BMP7 P18075 NOTCH2NLC Homo sapiens P0DPK4
Y2H Array
32296183
种属内
BMP7 P18075 NOTCH2NLC Homo sapiens P0DPK4
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 CYSRT1 Homo sapiens A8MQ03
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 CYSRT1 Homo sapiens A8MQ03
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP5-9 Homo sapiens P26371
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP5-9 Homo sapiens P26371
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 KRTAP5-9 Homo sapiens P26371
Validated Y2H
32296183
种属内
BMP7 P18075 TRIM27 Homo sapiens P14373
Y2H Array
31515488
种属内
BMP7 P18075 TRIM27 Homo sapiens P14373
Y2H Array
32296183
种属内
BMP7 P18075 TRIM27 Homo sapiens P14373
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 BEGAIN Homo sapiens Q9BUH8
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 BEGAIN Homo sapiens Q9BUH8
Validated Y2H
32296183
种属内
BMP7 P18075 BEGAIN Homo sapiens Q9BUH8
Y2H Array
32296183
种属内
BMP7 P18075 KHDRBS2 Homo sapiens Q5VWX1
Validated Y2H
32296183
种属内
BMP7 P18075 KHDRBS2 Homo sapiens Q5VWX1
Y2H Prey Pooling
32296183
种属内
BMP7 P18075 KHDRBS2 Homo sapiens Q5VWX1
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP3-1 Homo sapiens Q9BYR8
Validated Y2H
32296183
种属内
BMP7 P18075 KRTAP3-1 Homo sapiens Q9BYR8
Y2H Array
32296183
种属内
BMP7 P18075 KRTAP3-1 Homo sapiens Q9BYR8
Y2H Prey Pooling
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 BMP7 蛋白

目录号 产品名 蛋白编号 纯度
HY-P7008 BMP-7 Protein, Human P18075 (S293-H431) ≥95%
HY-P7008A BMP-7 Protein, Human (His) P18075 (S293-H431) ≥95%
HY-P700030AF Animal-Free BMP-7 Protein, Human (His) P18075 (M315-H431) ≥95%

关联疾病

疾病名称 别名
Congenital Heart Defects, Multiple Types, 4

CHTD4

Complete Atrioventricular Septal Defect-Tetralogy Of Fallot

Cavc-Tetralogy Of Fallot

Complete Avsd-Tetralogy Of Fallot

Complete Atrioventricular Canal Defect-Tetralogy Of Fallot

Complete Atrioventricular Septal Defect With Ventricular Hypoplasia

Cavc With Ventricular Hypoplasia

Complete Avsd With Ventricular Hypoplasia

Complete Atrioventricular Canal Defect With Ventricular Hypoplasia

Complete Atrioventricular Septal Defect With Ventricular Imbalance

Unbalanced Complete Atrioventricular Canal

Heart Defects, Congenital, Multiple Types, Type 4

Ventricular Septal Defect 1

VSD1

Renal Fibrosis
Ureteral Obstruction
Spondylolisthesis

Slipped Vertebrae

Acquired Spondylolisthesis

Spondylolysis

Acquired Spondylolysis

Osteochondritis Dissecans

Osteochondritis

Ocd

Konig Disease

Tactile Agnosia
Osteonecrosis

Bone Necrosis

Avascular Necrosis Of Bone

Aseptic Necrosis

Necrosis Of Bone Nos

Aseptic Osteonecrosis

Aseptic Necrosis Of Bone, Site Unspecified

Aseptic Or Avascular Bone Necrosis

Aseptic Necrosis Of Bone

Necrotic Bone

Necrotizing Bone

Spontaneous Osteonecrosis

Osteoradionecrosis

Osseous Heteroplasia, Progressive

Progressive Osseous Heteroplasia

POH

Osteoma Cutis

Familial Ectopic Ossification

Ectopic Ossification Familial Type

Ectopic Ossification

Heterotopic Ossification

Ectopic Ossification, Familial

Cutaneous Ossification

Myositis Ossificans Progressiva

Osteodermia

Osteosis Cutis

Ossification Heterotopic

Heteroplasia, Osseous, Progressive

Fibrodysplasia Ossificans Progressiva

Secondary Hyperparathyroidism

Hyperparathyroidism Secondary

Hyperparathyroidism, Secondary

Secondary Hyperparathyroidism Nec

Bone Disease

Bone Diseases

Skeletal Disease

Skeletal Disorder

Disorder Of Skeletal System

Nephrosclerosis

Renal Sclerosis

Kidney Disease

Renal Failure

Kidney Failure

Kidney Diseases

Nephropathy

Abnormality Of The Kidney

Impaired Renal Function Disease

Renal Anomaly

Kidney Dysfunction

Renal Disease

Nephropathies

Renal Failure Adverse Event

Abnormal Renal Function

Chronic Kidney Disease

Chronic Renal Disease

Chronic Kidney Failure

Ckd

Chronic Renal Failure

Kidney Failure, Chronic

Chronic Renal Failure Syndrome

Crf

Renal Failure - Chronic

Renal Failure Chronic

Chronic Kidney Diseases

Chronic Kidney Disease Stage 5

Ckd - [Chronic Kidney Disease]

Crf - [Chronic Renal Failure]

Chronic Kidney Impairment

Chronic Renal Impairment

Chronic Kidney Shutdown

Chronic Hypoxic Kidney Failure

Chronic Kidney Collapse

Chronic Renal Insufficiency

Chronic Kidney Toxaemia

Chronic Kidney Hypofunction

Chronic Renal Suppression

Chronic Renal Failure, Stage 5

Ckd - [Chronic Kidney Disease] Stage 5

End Stage Kidney Failure

End Stage Renal Failure

End Stage Kidney Disease

End Stage Renal Disease

End Stage Chronic Renal Failure

Esrf - [End Stage Renal Failure]

Esrd - [End Stage Renal Diseases]

Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²

Spinal Stenosis

Lumbar Spinal Stenosis

Cervical Spinal Stenosis

Spinal Stenosis Of Lumbar Region

Spinal Stenosis In Cervical Region

Spinal Canal Stenosis

Hypospadias

Hypospadias Familial

Familial Hypospadias

Sexual Masochism

Masochism

Pulmonary Hypertension

Primary Pulmonary Hypertension

Hypertension Pulmonary

Hypertension, Pulmonary

Hypertension, Pulmonary, Primary

Idiopathic Pulmonary Hypertension

Idiopathic Pulmonary Arterial Hypertension

Pulmonary Htn - [Hypertension]

Cardiomyopathy, Familial Restrictive, 3

RCM3

Restrictive Cardiomyopathy 3

Familial Restrictive Cardiomyopathy 3

Cardiomyopathy, Familial Restrictive 3

Cardiomyopathy, Restrictive, Familial, Type 3

Arthropathy

Ankylosis Of Ankle And Foot Joint

Ankylosis Of Forearm Joint

Ankylosis Of Hand Joint

Ankylosis Of Joint Of Ankle And/Or Foot

Ankylosis Of Joint Of Forearm

Ankylosis Of Joint Of Hand

Ankylosis Of Joint Of Lower Leg

Ankylosis Of Joint Of Multiple Sites

Ankylosis Of Joint Of Pelvic Region And Thigh

Ankylosis Of Joint Of Shoulder Region

Ankylosis Of Joint Of Upper Arm

Ankylosis Of Lower Leg Joint

Ankylosis Of Multiple Joints

Ankylosis Of Upper Arm Joint

Infectious Arthropathy

Joint Ankylosis Of The Ankle And Foot

Joint Ankylosis Of The Ankle And/Or Foot

Joint Ankylosis Of The Forearm

Joint Ankylosis Of The Hand

Joint Ankylosis Of The Lower Leg

Joint Ankylosis Of The Pelvic Region And Thigh

Joint Ankylosis Of The Shoulder Region

Joint Ankylosis Of The Upper Arm

Joint Diseases

Joint Disease

Arthropathy Associated With Infection

Ureteral Disease

Ureteral Diseases

Ureteral Disorders

Disorder Of Ureter

Proximal Symphalangism

Cushing'S Symphalangism

Symphalangism, Proximal

Hereditary Absence Of Proximal Interphalangeal Joints

Strasburger-Hawkins-Eldridge Syndrome

Strasburger-Hawkins-Eldridge-Hargrave-Mckusick Syndrome

Symphalangism, Proximal, 1a

Symphalangism, Proximal, 1b

Vessel'S Syndrome

Symphalangism, Cushing Type

Fibrodysplasia Ossificans Progressiva

Myositis Ossificans Progressiva

Progressive Myositis Ossificans

FOP

Progressive Ossifying Myositis

Myositis Ossificans

Stone Man Syndrome

Man Of Stone

Myositis Ossificans Progressive

Diffuse Progressive Ossifying Polymyositis

Fibrodysplasia Ossificans Congenita

Myositis Ossificans Progressiva, Site Unspecified

Münchmeyer Disease

Fop - [Fibrodysplasia Ossificans Progressiva]

Progressive Myositis Ossificans Calcification

Diffuse Pulmonary Fibrosis
Tarsal-Carpal Coalition Syndrome

TCC

Tarsal Carpal Coalition Syndrome

Nog-Related-Symphalangism Spectrum Disorder

Synostoses, Tarsal, Carpal, And Digital

Calcaneonavicular Coalition

Multiple Synostosis Syndrome

Synostoses, Tarsal, Carpal And Digital

Stroke, Ischemic

Cerebral Infarction

Stroke

Ischemic Stroke

Cerebrovascular Accident

Cerebral Infarction, Susceptibility To

Stroke, Ischemic, Susceptibility To

Cerebral Infarct

Ischemic Stroke, Susceptibility To

Stroke, Susceptibility To

Cva - Cerebral Infarction

ISCHSTR

Ischemic Cerebrovascular Accident

Dental Pulp Necrosis

Pulp Necrosis

Necrotic Pulp

Necrosis Of The Pulp

Dead Pulp

Devitalised Pulp

Putrescent Pulpitis

Devitalized Tooth

Dental Pulp Gangrene

Pulp Gangrene

Nonvital Tooth

Pulpless Tooth

Putrescent Pulp

Urinary Tract Obstruction

Obstructive Uropathy

Urinary Obstruction

Urologic Diseases

Endocardial Fibroelastosis

Endomyocardial Fibroelastosis

Elastomyofibrosis

EFE

Efe - [Endocardial Fibroelastosis]

Primary Endocardial Fibroelastosis

Fibroelastosis Cordis

Fetal Endocarditis

Fibroelastosis

Congenital Endocardial Fibroelastosis

Congenital Valvular Endocarditis

Ischemic Bone Disease
Bone Deterioration Disease
Palmoplantar Keratoderma, Nonepidermolytic, Focal Or Diffuse

PPKNEFD

Focal Or Diffuse Nonepidermolytic Palmoplantar Keratoderma

Autosomal Dominant Focal Non-Epidermolytic Palmoplantar Keratoderma With Plantar Blistering

Palmoplantar Keratoderma, Non-Epidermolytic, Focal Or Diffuse

Nonepidermolytic Focal Or Diffuse Palmoplantar Keratoderma

Keratoderma, Palmoplantar, Nonepidermolytic, Focal Or Diffuse

Dental Pulp Disease

Dental Pulp Diseases

Dental Pulp Disorder

Disorder Of Pulp Of Tooth

Pulp Disorder

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

Prostate Cancer

Prostate Carcinoma

Prostate Cancer, Familial

Prostate Neoplasm

Prostate Cancer, Somatic

Prostate Cancer, Susceptibility To

Prostatic Cancer

Prostatic Neoplasms

Hereditary Prostate Cancer

Prostatic Neoplasm

Cancer Of Prostate

Carcinoma Of Prostate

Familial Prostate Cancer

Familial Prostate Carcinoma

Malignant Tumor Of Prostate

Malignant Neoplasm Of Prostate

Prostate Cancer, Familial, Susceptibility To

Malignant Tumor Of The Prostate

Ngp - New Growth Of Prostate

Tumor Of The Prostate

Prostate Cancer, Hereditary

Cancer Of The Prostate

Malignant Neoplasm Of The Prostate

Prostatic Carcinoma

PC

Prca

Cancer, Prostate

Malignant Prostatic Tumour

Malignant Tumour Of Prostate

Primary Prostate Cancer

Primary Malignant Neoplasm Of Prostate

Prostate Gland Cancer

Anus, Imperforate

Imperforate Anus

Anorectal Malformation

Anal Atresia

Anorectal Malformations

Congenital Atresia Of Anus

Congenital Or Infantile Occlusion Of Anus

Anal Stenosis

Arm

Diabetes Mellitus

Diabetes

Osteogenic Sarcoma

Osteosarcoma

OSRC

Osteosarcoma, Somatic

Neoplasms, Bone Tissue

Bone Tissue Neoplasm

Osteoid Sarcoma

Skeletal Sarcoma

Osteosarcoma Of Bone

Bone Sarcoma

Bone Structure Disease
Cleft Palate, Isolated

Cleft Palate

Isolated Cleft Palate

CPI

Cp

Palatoschisis

Cleft Palate Isolated

Uranostaphyloschisis

Congenital Fissure Of Palate

Cleft Of Secondary Palate

Thyroid Gland Anaplastic Carcinoma

Anaplastic Thyroid Carcinoma

Anaplastic Thyroid Cancer

Thyroid Cancer, Anaplastic

Thyroid Carcinoma, Anaplastic

Thyroid Carcinoma Anaplastic

Inflammatory Bowel Disease

Inflammatory Bowel Diseases

Bowel Disease, Inflammatory

Geotrichosis
Coloboma Of Macula

Coloboma

Congenital Ocular Coloboma

Microphthalmia, Isolated, With Coloboma

Agenesis Of Macula

Hereditary Macular Coloboma

Ocular Coloboma

Coloboma Of Eye

Macular Coloboma

Uveoretinal Coloboma

Uruguay Faciocardiomusculoskeletal Syndrome

FCMSU

Faciocardiomusculoskeletal Syndrome, Uruguay Type

Fcms

Musculoskeletal Diseases

Alport Syndrome

Hereditary Nephritis

Alport Syndrome, X-Linked

Hemorrhagic Hereditary Nephritis

Congenital Hereditary Hematuria

Hemorrhagic Familial Nephritis

Familial Nephritis

Thin Basement Membrane Disease

Thin Basement Membrane Nephropathy

Hematuria-Nephropathy-Deafness Syndrome

Hematuric Hereditary Nephritis

Hereditary Familial Congenital Hemorrhagic Nephritis

Hereditary Hematuria Syndrome

Hereditary Interstitial Pyelonephritis

Alport Deafness-Nephropathy

Alport Hearing Loss-Nephropathy

Alports Syndrome

Nephritis, Hereditary

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

Orofacial Cleft

Cleft, Orofacial

Cakut

Renal Or Urinary Tract Malformation

Congenital Anomalies Of Kidney And Urinary Tract

Congenital Anomaly Of Kidney And Urinary Tract

Congenital Anomalies Of The Kidney And Urinary Tract

Kidney And Urinary Tract, Anomalies, Congenital

Renal Hypodysplasia, Nonsyndromic, 1

Chromosome 2q35 Duplication Syndrome

Syndactyly

Syndactyly Type 1

Sdty1

Zygodactyly

Syndactyly, Type I

Sd1

Syndactyly, Type 1, With Or Without Craniosynostosis

Symphalangism

Non-Syndromic Syndactyly

Symphalangy

Webbing Of Digits

Syndactyly, Type 1

Brittle Bone Disorder

Osteogenesis Imperfecta

Brittle Bone Disease

Fragilitas Ossium

Osteopsathyrosis

Lobstein Disease

Oi

Vrolik Disease

Lobstein'S Disease

Lobstein'S Syndrome

Vrolik'S Disease

Porak And Durante Disease

Glass Bone Disease

Osteogenesis Imperfecta, Dominant Perinatal Lethal

Osteogenesis Imperfecta, Recessive Perinatal Lethal

Brittle Bone Syndrome

Oi - [Osteogenesis Imperfecta]

Ossium Fragility

Osteitis Fragilitans

Bony Fragility

Blue Sclera With Fragility Of Bone And Deafness

White Blue Sclera - Fragility Of Bone - Deafness

Osteochondrodysplasia

Skeletal Dysplasia

Chondrodystrophy

Congenital Anomaly Of Cartilage

Osteochondrodysplasias

Cartilage Development Disorder

Osteochondrodysplasia Syndrome

Dysplasia, Skeletal

Mucopolysaccharidosis Iv

Tooth Agenesis

Oligodontia

Hypodontia

Selective Tooth Agenesis

Tooth Agenesis, Selective

Familial Tooth Agenesis

Anodontia

Congenital Absence Of One Tooth

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 ID
Mus musculus BMP7 MGD MGI:103302
Macaca mulatta BMP7 VGNC VGNC:70266
Felis catus BMP7 VGNC VGNC:60135
Bos taurus BMP7 VGNC VGNC:26522
Rattus norvegicus BMP7 RGD RGD:620743
Canis familiaris BMP7 VGNC VGNC:38482