1. Gene
  2. MYH4 - myosin heavy chain 4 Gene

MYH4 - myosin heavy chain 4 Gene

中文名称:肌球蛋白重链 4

种属: Homo sapiens

同用名: MYH2B; MyHC-2B; MyHC-IIb

基因 ID: 4622 | 基因类型: protein coding

关于 MYH4

Cytogenetic location: 17p13.1 Genomic coordinates (GRCh38): 17:10,443,263-10,469,559 (from NCBI)

This gene has 1 transcript (splice variant), 63 orthologues and 43 paralogues. Low expression observed in reference dataset.

功能概要

启用双链 RNA 结合活性。参与肌肉收缩。位于肌原纤维中。 [由基因组资源联盟提供,2022 年 4 月]

Enables double-stranded RNA binding activity. Involved in muscle contraction. Located in myofibril. [provided by Alliance of Genome Resources, Apr 2022]

MYH4 基因产物(1)

mRNA Protein Name
NM_017533.2 NP_060003.2 myosin-4
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 double-stranded RNA binding IDA
IDA: 通过直接分析推断
21266579 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in muscle contraction IDA
IDA: 通过直接分析推断
8145163 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in myofibril IDA
IDA: 通过直接分析推断
8145163 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

MYH4 蛋白结构

Myosin_N

Myosin_N: Myosin N-terminal SH3-like domain (35 - 76)

Myosin_head

Myosin_head: Myosin head (motor domain) (89 - 770)

Myosin_tail_1

Myosin_tail_1: Myosin tail (1072 - 1929)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1500
  • 1800
  • 1939 a.a.
蛋白主名 其他名称

myosin-4

myosin heavy chain 2b

关联疾病

疾病名称 别名
Arthrogryposis, Distal, Type 7

Hecht Syndrome

Trismus-Pseudocamptodactyly Syndrome

Distal Arthrogryposis Type 7

Dutch-Kentucky Syndrome

DA7

Hecht-Beals Syndrome

Mouth, Inability To Open Completely, And Short Finger-Flexor Tendons

Mouth, Inability To Completely Open, And Short Finger-Flexor Tendons

Arthrogryposis Distal Type 7

Trismus Pseudocamptodactyly Syndrome

Arthrogryposis, Distal, 7

Distal Arthrogryposis

Arthrogryposis Multiplex Congenita

Arthrogryposis

Congenital Multiple Arthrogryposis

Congenital Arthromyodysplasia

Fibrous Ankylosis Of Multiple Joints

Guerin-Stern Syndrome

Guérin-Stern Syndrome

Myodystrophia Fetalis Deformans

Otto Syndrome

Rocher-Sheldon Syndrome

Rossi Syndrome

Amc

Multiple Congenital Arthrogryposis

Arthrogryposis Syndrome

Arthrogryposis, Distal

Distal Arthrogryposis Syndrome

Freeman-Sheldon Syndrome

Arthrogryposis, Distal, Type 2b

Congenital Multiplex Arthrogryposis

Amyoplasia Congenita

Congenital Amyoplasia

Amc - [Arthrogryposis Multiplex Congenita]

Congenital Fiber-Type Disproportion

Congenital Fiber Type Disproportion

Cftdm

Congenital Myopathy With Fiber Type Disproportion

Cftd

Congenital Fiber-Type Disproportion Myopathy

Fiber-Type Disproportion Myopathy, Congenital

Myopathy, Congenital With Fiber-Type Disproportion

Cardiomyopathy, Familial Hypertrophic, 1

Asymmetric Septal Hypertrophy

Familial Hypertrophic Cardiomyopathy

Hypertrophic Cardiomyopathy 1

CMH1

Hypertrophic Cardiomyopathy 19

CMH

Ventricular Hypertrophy, Hereditary

Ash

Hypertrophic Subaortic Stenosis, Idiopathic

Cardiomyopathy, Familial Hypertrophic

Cardiomyopathy, Hypertrophic, 1, Digenic

Cardiomyopathy, Familial Hypertrophic 1

Hcm

Hereditary Ventricular Hypertrophy

Idiopathic Hypertrophic Subaortic Stenosis

Hypertrophic Cardiomyopathy

Cardiomyopathy, Hypertrophic, Familial

Cardiomyopathy, Hypertrophic, 1

Familial Asymmetric Septal Hypertrophy

Heritable Hypertrophic Cardiomyopathy

Fhc

Cardiomyopathy, Hypertrophic, Familial, Type 1

Hypertrophic Cardiomyopathy

Hypertrophic Obstructive Cardiomyopathy

Cardiomyopathy, Hypertrophic

Cardiomyopathy Hypertrophic Obstructive

Cardiomyopathy, Hypertrophic, Familial

Idiopathic Myocardial Hypertrophy

Idiopathic Hypertrophic Cardiomyopathy

Obstructive Idiopathic Hypertrophic Cardiomyopathy

Obstructive Cardiomyopathy

Idiopathic Hypertrophic Subaortic Stenosis

Muscular Subaortic Stenosis

Hypertrophic Obstructive Subaortic Stenosis

Myopathy

Muscular Diseases

Myopathies

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

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 MYH4 MGD MGI:1339713
Macaca mulatta MYH4 VGNC VGNC:75100
Canis familiaris MYH4 VGNC VGNC:54972
Rattus norvegicus MYH4 RGD RGD:3139
Bos taurus MYH4 VGNC VGNC:55854
Felis catus MYH4 VGNC VGNC:99285