1. Gene
  2. ANKRD1 - ankyrin repeat domain 1 Gene

ANKRD1 - ankyrin repeat domain 1 Gene

中文名称:锚蛋白重复结构域 1

种属: Homo sapiens

同用名: ALRP; CARP; C-193; CVARP; MCARP; bA320F15.2

基因 ID: 27063 | 基因类型: protein coding

关于 ANKRD1

Cytogenetic location: 10q23.31 Genomic coordinates (GRCh38): 10:90,912,096-90,921,087 (from NCBI)

This gene has 1 transcript (splice variant), 243 orthologues, 1 paralogue and is associated with 1 phenotype. Restricted expression toward heart (RPKM 2170.6).

功能概要

由该基因编码的蛋白质定位于内皮细胞的细胞核,并由 IL-1 和 TNF-α 刺激诱导。对大鼠心肌细胞的研究表明,该基因起着转录因子的作用。这种蛋白质与肌节蛋白肌钯蛋白和肌联蛋白之间的相互作用表明它也可能参与肌原纤维牵张传感器系统。[RefSeq 提供,2008 年 7 月]

The protein encoded by this gene is localized to the nucleus of endothelial cells and is induced by IL-1 and TNF-alpha stimulation. Studies in rat cardiomyocytes suggest that this gene functions as a transcription factor. Interactions between this protein and the sarcomeric proteins myopalladin and titin suggest that it may also be involved in the myofibrillar stretch-sensor system. [provided by RefSeq, Jul 2008]

ANKRD1 基因产物(1)

mRNA Protein Name
NM_014391.3 NP_055206.2 ankyrin repeat domain-containing protein 1
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 DNA binding IDA
IDA: 通过直接分析推断
7730328 GOA
enables R-SMAD binding IPI
IPI: 通过物理相互作用推断
20599664 GOA
enables RNA polymerase II-specific DNA-binding transcription factor binding IPI
IPI: 通过物理相互作用推断
20599664 GOA
enables histone deacetylase binding IPI
IPI: 通过物理相互作用推断
20599664 GOA
enables p53 binding IPI
IPI: 通过物理相互作用推断
20599664 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
11309420 GOA
enables titin binding IPI
IPI: 通过物理相互作用推断
14583192 GOA
enables transcription coactivator activity IDA
IDA: 通过直接分析推断
20599664 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in cytoplasm IDA
IDA: 通过直接分析推断
12054667 GOA
located in cytosol IDA
IDA: 通过直接分析推断
19608030 GOA
located in nucleus IDA
IDA: 通过直接分析推断
7730328 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

ANKRD1 蛋白结构

Ank_2

Ank_2: Ankyrin repeats (3 copies) (127 - 216)

Ank_2

Ank_2: Ankyrin repeats (3 copies) (220 - 282)

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

ankyrin repeat domain-containing protein 1

ankyrin repeat domain 1 (cardiac muscle)

ANKRD1 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
Intra ANKRD1 Q15327 NAGK Homo sapiens Q9UJ70-2
Validated Y2H
32296183
Intra ANKRD1 Q15327 NAGK Homo sapiens Q9UJ70-2
Y2H Array
32296183
Intra ANKRD1 Q15327 NAGK Homo sapiens Q9UJ70-2
Y2H Prey Pooling
32296183
Intra ANKRD1 Q15327 SPANXN2 Homo sapiens Q5MJ10
Validated Y2H
32296183
Intra ANKRD1 Q15327 MEOX2 Homo sapiens Q6FHY5
Y2H Prey Pooling
32296183
Intra ANKRD1 Q15327 MEOX2 Homo sapiens Q6FHY5
Validated Y2H
32296183
Intra ANKRD1 Q15327 MEOX2 Homo sapiens Q6FHY5
Y2H Array
32296183
Intra ANKRD1 Q15327 CDCA7L Homo sapiens Q96GN5
Validated Y2H
32296183
Intra ANKRD1 Q15327 MAPRE3 Homo sapiens Q9UPY8
Validated Y2H
32296183
Intra ANKRD1 Q15327 ZNF446 Homo sapiens Q9NWS9-2
Y2H Prey Pooling
32296183
Intra ANKRD1 Q15327 ZNF446 Homo sapiens Q9NWS9-2
Validated Y2H
32296183
Intra ANKRD1 Q15327 ZNF446 Homo sapiens Q9NWS9-2
Y2H Array
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Familial Isolated Dilated Cardiomyopathy

Familial Or Idiopathic Dilated Cardiomyopathy

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

Total Anomalous Pulmonary Venous Return 1

Scimitar Syndrome

Total Anomalous Pulmonary Venous Return

Anomalous Pulmonary Venous Return

Scimitar Anomaly

TAPVR1

Apvr

Halasz Syndrome

Hypogenetic Lung Syndrome

Pulmonary Venolobar Syndrome

TAPVR

Congenital Total Pulmonary Venous Return Anomaly

Congenital Venolobar Syndrome

Mirror-Image Lung Syndrome

Vena Cava Bronchovascular Syndrome

Pulmonary Venous Return Anomaly

Congenital Pulmonary Venolobar Syndrome

Epibronchial Right Pulmonary Vein Syndrome

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

Muscular Dystrophy

Muscular Dystrophies

Congenital Md

Congenital Muscular Dystrophy

Cmd

Mdc

Dystrophy, Muscular

Gower'S Muscular Dystrophy

Progressive Musclular Dystrophy

Pseudohypertrophic Atrophy

Pseudohypertrophic Muscle Paralysis

Pseudohypertrophic Muscular Atrophy

Pseudohypertrophic Muscular Dystrophy

Pseudohypertrophic Paralysis

Pseudomuscular Hypertrophy

Sciatic Neuropathy
Lesion Of Sciatic Nerve

Nerve Lesion Sciatic

Sciatic Neuropathy

Mononeuritis Of Lower Limb
Restrictive Cardiomyopathy

Familial Restrictive Cardiomyopathy

Cardiomyopathy, Restrictive

Cardiomyopathy, Constrictive

Primary Restrictive Cardiomyopathy

Rcm

Cardiomyopathy Restrictive

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

Meningioma, Familial

Meningioma

Familial Meningioma

Meningioma, Familial, Susceptibility To

Meningeal Neoplasm

Meningeal Neoplasms

Meningiomas

Meningioma, Nf2-Related, Somatic

Meningioma, Sis-Related

Meningothelial Cell Tumor

Neoplasm Of The Meninges

Primary Meningeal Tumor

Familial Multiple Meningioma

MNGMA

Meningioma, Benign, No Icd-O Subtype

Intracranial Meningioma

Meningothelial Cell Neoplasm

Supratentorial Meningioma

Primary Neoplasm Of Spinal Meninges

Benign Intracranial Meningioma

Benign Meningioma

Meningeal Tumours

Meningeal Sarcoma Of Unspecified Site

Meningothelial Sarcoma Of Unspecified Site

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

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
Rattus norvegicus ANKRD1 RGD RGD:61989
Bos taurus ANKRD1 VGNC VGNC:25908
Canis familiaris ANKRD1 VGNC VGNC:37880
Macaca mulatta ANKRD1 VGNC VGNC:69616
Mus musculus ANKRD1 MGD MGI:1097717
Felis catus ANKRD1 VGNC VGNC:97350