1. Gene
  2. WNT5A - Wnt family member 5A Gene

WNT5A - Wnt family member 5A Gene

中文名称:Wnt 家族成员 5A

种属: Homo sapiens

同用名: hWNT5A

基因 ID: 7474 | 基因类型: protein coding

关于 WNT5A

Cytogenetic location: 3p14.3 Genomic coordinates (GRCh38): 3:55,465,715-55,505,263 (from NCBI)

This gene has 7 transcripts (splice variants), 214 orthologues, 18 paralogues and is associated with 3 phenotypes. Broad expression in urinary bladder (RPKM 9.1), endometrium (RPKM 7.3) and 19 other tissues.

功能概要

Wnt 基因家族由编码分泌信号蛋白的结构相关基因组成。这些蛋白质与肿瘤发生和几个发育过程有关,包括胚胎发生过程中细胞命运和模式的调节。该基因编码 Wnt 家族的一个成员,该成员通过规范和非规范 Wnt 通路发出信号。该蛋白是七种跨膜受体 Frizzled-5 和酪氨酸激酶孤儿受体 2 的配体。该蛋白在胚胎发生过程中调节发育途径中起着至关重要的作用。这种蛋白质也可能在肿瘤发生中发挥作用。该基因的突变是常染色体显性罗宾诺综合征的原因。交替剪接导致多个转录本变体。[RefSeq 提供,2012 年 1 月]

The Wnt gene family consists of structurally related genes which encode secreted signaling proteins. These proteins have been implicated in oncogenesis and in several developmental processes, including regulation of cell fate and patterning during embryogenesis. This gene encodes a member of the Wnt family that signals through both the canonical and non-canonical Wnt pathways. This protein is a ligand for the seven transmembrane receptor Frizzled-5 and the tyrosine kinase orphan receptor 2. This protein plays an essential role in regulating developmental pathways during embryogenesis. This protein may also play a role in oncogenesis. Mutations in this gene are the cause of autosomal dominant Robinow syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]

WNT5A 基因产物(4)

mRNA Protein Name
NM_001256105.1 NP_001243034.1 protein Wnt-5a isoform 2 precursor
NM_001377271.1 NP_001364200.1 protein Wnt-5a isoform 2 precursor
NM_001377272.1 NP_001364201.1 protein Wnt-5a isoform 2 precursor
NM_003392.7 NP_003383.4 protein Wnt-5a isoform 1 precursor
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 frizzled binding IPI
IPI: 通过物理相互作用推断
18174455 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
22784633 GOA
enables receptor tyrosine kinase-like orphan receptor binding IPI
IPI: 通过物理相互作用推断
18287027 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in Wnt signaling pathway IDA
IDA: 通过直接分析推断
20034610 GOA
involved in Wnt signaling pathway, calcium modulating pathway IMP
IMP: 通过突变表型推断
17986384 GOA
acts upstream of activation of protein kinase B activity IDA
IDA: 通过直接分析推断
20034610 GOA
involved in cellular response to calcium ion IEP
IEP: 通过表达模式推断
18703641 GOA
involved in cellular response to lipopolysaccharide IEP
IEP: 通过表达模式推断
18174455 GOA
involved in cellular response to transforming growth factor beta stimulus IEP
IEP: 通过表达模式推断
15040835 GOA
involved in cellular response to type II interferon IEP
IEP: 通过表达模式推断
18174455 GOA
involved in embryonic skeletal system development IMP
IMP: 通过突变表型推断
19918918 GOA
involved in epithelial to mesenchymal transition IEP
IEP: 通过表达模式推断
12841867 GOA
involved in face development IMP
IMP: 通过突变表型推断
19918918 GOA
involved in genitalia development IMP
IMP: 通过突变表型推断
19918918 GOA
involved in hematopoietic stem cell proliferation IDA
IDA: 通过直接分析推断
9787155 GOA
involved in inflammatory response IMP
IMP: 通过突变表型推断
31512787 GOA
involved in keratinocyte differentiation IEP
IEP: 通过表达模式推断
19399181 GOA
involved in macrophage derived foam cell differentiation IMP
IMP: 通过突变表型推断
31512787 GOA
involved in male gonad development IEP
IEP: 通过表达模式推断
17848411 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: 通过直接分析推断
19277043 GOA
involved in negative regulation of apoptotic process IDA
IDA: 通过直接分析推断
19251946 GOA
acts upstream of or within negative regulation of canonical Wnt signaling pathway IGI
IGI: 通过遗传相互作用推断
12952940 GOA
involved in negative regulation of fat cell differentiation IMP
IMP: 通过突变表型推断
20032469 GOA
involved in negative regulation of mesenchymal cell proliferation IDA
IDA: 通过直接分析推断
19878652 GOA
involved in phospholipase C-activating G protein-coupled receptor signaling pathway IMP
IMP: 通过突变表型推断
19099253 GOA
involved in positive regulation of DNA-templated transcription IMP
IMP: 通过突变表型推断
19847889 GOA
acts upstream of positive regulation of JUN kinase activity IDA
IDA: 通过直接分析推断
20034610 GOA
involved in positive regulation of MAPK cascade IMP
IMP: 通过突变表型推断
20032469 GOA
involved in positive regulation of NF-kappaB transcription factor activity IDA
IDA: 通过直接分析推断
18287027 GOA
involved in positive regulation of T cell chemotaxis IMP
IMP: 通过突变表型推断
19520808 GOA
involved in positive regulation of angiogenesis IMP
IMP: 通过突变表型推断
17035633 GOA
involved in positive regulation of chemokine production IMP
IMP: 通过突变表型推断
19520808 GOA
involved in positive regulation of cytokine production involved in immune response IMP
IMP: 通过突变表型推断
18174455 GOA
involved in positive regulation of endothelial cell migration IMP
IMP: 通过突变表型推断
17035633 GOA
involved in positive regulation of endothelial cell proliferation IMP
IMP: 通过突变表型推断
17986384 GOA
involved in positive regulation of fibroblast proliferation IDA
IDA: 通过直接分析推断
19251946 GOA
involved in positive regulation of inflammatory response IMP
IMP: 通过突变表型推断
18174455 GOA
involved in positive regulation of interleukin-1 beta production IMP
IMP: 通过突变表型推断
18174455 GOA
involved in positive regulation of interleukin-6 production IMP
IMP: 通过突变表型推断
18174455 GOA
involved in positive regulation of macrophage activation IMP
IMP: 通过突变表型推断
18174455 GOA
involved in positive regulation of macrophage cytokine production IMP
IMP: 通过突变表型推断
18174455 GOA
involved in positive regulation of ossification IMP
IMP: 通过突变表型推断
20032469 GOA
acts upstream of or within positive regulation of protein catabolic process IGI
IGI: 通过遗传相互作用推断
12952940 GOA
involved in positive regulation of protein kinase C activity IMP
IMP: 通过突变表型推断
12086864 GOA
involved in positive regulation of response to cytokine stimulus IDA
IDA: 通过直接分析推断
19399181 GOA
involved in positive regulation of transcription by RNA polymerase II IMP
IMP: 通过突变表型推断
18174455 GOA
involved in positive regulation of type I interferon-mediated signaling pathway IDA
IDA: 通过直接分析推断
19399181 GOA
involved in protein localization IDA
IDA: 通过直接分析推断
19177143 GOA
involved in regulation of postsynapse organization IDA
IDA: 通过直接分析推断
27402827 GOA
involved in regulation of postsynapse organization IMP
IMP: 通过突变表型推断
27402827 GOA
involved in regulation of postsynaptic cytosolic calcium ion concentration IDA
IDA: 通过直接分析推断
27402827 GOA
involved in regulation of postsynaptic cytosolic calcium ion concentration IMP
IMP: 通过突变表型推断
27402827 GOA
involved in regulation of synapse organization IDA
IDA: 通过直接分析推断
18986540 GOA
involved in regulation of synapse organization IMP
IMP: 通过突变表型推断
18986540 GOA
involved in secondary palate development IMP
IMP: 通过突变表型推断
18413325 GOA
involved in wound healing IDA
IDA: 通过直接分析推断
19878652 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
18703641 GOA
is active in glutamatergic synapse IDA
IDA: 通过直接分析推断
18986540 GOA
is active in glutamatergic synapse IMP
IMP: 通过突变表型推断
18986540 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

WNT5A 蛋白结构

wnt

wnt: wnt family (68 - 380)

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

protein Wnt-5a

WNT-5A protein

关联疾病

疾病名称 别名
Robinow Syndrome, Autosomal Dominant 1

Autosomal Dominant Robinow Syndrome 1

DRS1

Robinow Dwarfism

Fetal Face Syndrome

Acral Dysostosis With Facial And Genital Abnormalities

Robinow, Autosomal Dominant Syndrome, Type 1

Autosomal Dominant Robinow Syndrome

Fetal Face Syndrome

Robinow Syndrome, Autosomal Dominant

Robinow Syndrome

Acral Dysostosis With Facial And Genital Abnormalities

Fetal Face Syndrome

Robinow Dwarfism

Mesomelic Dwarfism-Small Genitalia Syndrome

Robinow-Silverman-Smith Syndrome

Costovertebral Segmentation Defect With Mesomelia

Covesdem Syndrome

Robinow'S Syndrome

Robinow-Silverman Syndrome

Robinow Syndrome, Autosomal Recessive 1

Robinow Syndrome, Autosomal Recessive

Autosomal Recessive Robinow Syndrome

Covesdem Syndrome

RRS1

Costovertebral Segmentation Defect-Mesomelia Syndrome

Rrs

Costovertebral Segmentation Defect With Mesomelia, Formerly

Covesdem Syndrome, Formerly

Costovertebral Segmentation Defect With Mesomelia

Robinow Syndrome Autosomal Recessive With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals

Robinow Syndrome Autosomal Recessive With Brachy-Syn-Polydactyly

Robinow Syndrome, Autosomal Recessive, With Aplasia/Hypoplasia Of Phalanges And Metacarpals/Metatarsals

Robinow Syndrome, Autosomal Recessive, With Brachy-Syn-Polydactyly

Robinow, Autosomal Recessive Syndrome, Type 1

Brachydactyly, Type B1

Brachydactyly Type B1

Brachydactyly Type B

BDB1

Brachydactyly, Type B

Bdb

Brachydactyly B1

Achondroplasia

Achondroplastic Dwarfism

ACH

Osteosclerosis Congenita

Achondroplastic Physique

Chondrodystrophia

Dwarf, Achondroplastic

Achondroplastic Short Stature

Congenital Osteosclerosis

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

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

Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

Melanoma

Malignant Melanoma

Cutaneous Melanoma

Naevocarcinoma

Malignant Melanomas

Hepatocellular Carcinoma

Liver Cancer

Primary Liver Cancer

HCC

Hepatoma

Malignant Neoplasm Of Liver

Liver Neoplasms

Cancer, Hepatocellular

Liver Cell Carcinoma

Lcc

Hepatoblastoma, Somatic

Hepatic Cancer

Primary Malignant Neoplasm Of Liver

Rare Tumor Of Liver And Intrahepatic Biliary Tract

Hepatocellular Carcinoma, Somatic

Hepatocellular Carcinoma, Childhood Type, Somatic

Hepatocellular Cancer, Somatic

Ca Liver - Primary

Hepatic Neoplasm

Malignant Hepato-Biliary Neoplasm

Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary

Malignant Neoplasm Of Liver, Primary

Malignant Tumor Of Liver

Neoplasm Of Liver

Non-Resectable Primary Hepatic Malignant Neoplasm

Resectable Malignant Neoplasm Of Liver

Resectable Malignant Neoplasm Of The Liver

Primary Liver Carcinoma

Primary Malignant Liver Neoplasm

Primary Cancer Of Liver

Primary Tumor Of The Liver

Rare Tumor Of Liver And Ibt

Hepatocellular Cancer

Neoplasm Of The Liver

Carcinoma, Hepatocellular

Hepatomas

Liver Neoplasm

Liver Carcinoma

Liver And Intrahepatic Biliary Tract Carcinoma

Malignant Hepatobiliary Neoplasm

Adult Primary Hepatocellular Carcinoma

Hepatoblastoma

Carcinoma Of Liver

Malignant Liver Tumour

Malignant Hepatic Tumour

Omodysplasia

Omodysplasia Type 1

Omodysplasia 2

Gallbladder Melanoma

Malignant Melanoma Of Gallbladder

Focal Dermal Hypoplasia

Goltz Syndrome

Goltz-Gorlin Syndrome

FDH

FODH

Dhof

Goltz Gorlin Syndrome

Hypoplasia, Dermal, Focal

Tetraamelia Syndrome

Tetra-Amelia Syndrome

Tetraamelia-Multiple Malformations Syndrome

Tetra-Amelia

Tetra-Amelia, Autosomal Recessive

Tetraamelia, Autosomal Recessive

Total Amelia

Zimmer Phocomelia

Tetams

Zimmer Taub Sova Syndrome

Neural Tube Defects

Spina Bifida

Neural Tube Defect

NTD

Neural Tube Defects, Susceptibility To

Spinal Dysraphism

Spina Bifida, Susceptibility To

Rachischisis

Cleft Spine

Open Spine

Hydrocele Spinalis

Neural Tube Defect Nos

Sb - [Spina Bifida]

Spinal Hernia Nos

Spinal Fissure Nos

Exudative Vitreoretinopathy

Familial Exudative Vitreoretinopathy

Fevr

Criswick-Schepens Syndrome

Exudative Vitreoretinopathy, Familial

Vitreoretinopathy, Exudative )

Exudative Vitreoretinopathy 1

Osteoporosis

Postmenopausal Osteoporosis

Osteoporosis, Postmenopausal

Bone Mineral Density Quantitative Trait Locus

Bmnd

Osteoporosis, Involutional

Osteoporosis, Susceptibility To

Osteoporosis, Postmenopausal, Susceptibility

Bone Mineral Density Variation Qtl, Osteoporosis

OSTEOP

Involutional Osteoporosis

Senile Osteoporosis

Osteoporosis Postmenopausal

Bone Mineral Density, Quantitative Trait Locus

Osteoporosis, Senile

Idiopathic Osteoporosis

Bone Rarefaction Nos

Type 1 Osteoporosis

Cleft Palate, Isolated

Cleft Palate

Isolated Cleft Palate

CPI

Cp

Palatoschisis

Cleft Palate Isolated

Uranostaphyloschisis

Congenital Fissure Of Palate

Cleft Of Secondary Palate

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

Norrie Disease

Atrophia Bulborum Hereditaria

Episkopi Blindness

Pseudoglioma

ND

Norrie-Warburg Disease

Anderson-Warburg Syndrome

Fetal Iritis Syndrome

Norrie Syndrome

Norrie-Warburg Syndrome

Ndp

Congenital Progressive Oculo-Acoustico-Cerebral Degeneration

Norrie'S Disease

Oligophrenia Microphthalmus

Pseudoglioma Congenita

Whitnall-Norman Syndrome

Medulloblastoma

MDB

Cpnet

Localized Primitive Neuroectodermal Tumor

Classic Medulloblastoma

Medulloblastoma Predisposition Syndrome

Medulloblastoma, Somatic

Brain Medulloblastoma

Cns Pnet

Infratentorial Primitive Neuroectodermal Tumor

Neuroectodermal Tumors, Primitive

Medulloblastomas

Desmoplastic Medulloblastoma

Medulloblastoma, With Extensive Nodularity

Medulloblastoma Of Unspecified Site

Medullomyoblastoma Of Unspecified Site

Ovarian Cancer

Ovarian Carcinoma

Ovarian Neoplasm

Malignant Tumour Of Ovary

Cancer Of The Ovary

Epithelial Ovarian Cancer

Neoplasm Of Ovary

Ovarian Neoplasms

Ovarian Cancers

Malignant Neoplasm Of Ovary

Primary Malignant Neoplasm Of Ovary

Ovarian Cancer, Somatic

Malignant Ovarian Tumor

Ovary Neoplasm

Primary Ovarian Cancer

Tumor Of The Ovary

Malignant Neoplasm Of The Ovary

Malignant Tumor Of The Ovary

Ovarian Malignant Tumor

OC

Ovarian Carcinomas

Cancer, Ovarian

Cancer Of Ovary

Ovary Cancer

Ca Ovary

Fallopian Tube Serous Adenocarcinoma
Psoriasis 11

PSORS11

Psoriasis Susceptibility 11

Psoriasis

Psoriasis Vulgaris

Psoriasis 11, Susceptibility To

Pv

Orofacial Cleft

Cleft, Orofacial

Brachydactyly
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

Strabismus

Strabismus, Susceptibility To

Strabismus, Susceptibility To, 1

Strabismus 1

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
Bos taurus WNT5A VGNC VGNC:36960
Macaca mulatta WNT5A VGNC VGNC:110318
Rattus norvegicus WNT5A RGD RGD:69250
Mus musculus WNT5A MGD MGI:98958
Felis catus WNT5A VGNC VGNC:102731
Canis familiaris WNT5A VGNC VGNC:48425
Others WNT5A NCBI