1. Gene
  2. SQSTM1 - sequestosome 1 Gene

SQSTM1 - sequestosome 1 Gene

中文名称:sequestosome 1

种属: Homo sapiens

同用名: p60; p62; A170; DMRV; OSIL; PDB3; ZIP3; p62B; NADGP; FTDALS3

基因 ID: 8878 | 基因类型: protein coding

关于 SQSTM1

Cytogenetic location: 5q35.3 Genomic coordinates (GRCh38): 5:179,806,393-179,838,078 (from NCBI)

This gene has 16 transcripts (splice variants), 1 gene allele, 212 orthologues and is associated with 9 phenotypes. Ubiquitous expression in thyroid (RPKM 57.3), gall bladder (RPKM 54.3) and 25 other tissues.

功能概要

该基因编码一种多功能蛋白,可结合泛素并调节核因子 kappa-B (NF-kB) 信号通路的激活。该蛋白质作为支架/衔接蛋白与 TNF 受体相关因子 6 协同作用,以响应上游信号介导 NF-kB 的激活。已经为该基因鉴定了编码相同或不同同种型的可变剪接转录物变体。该基因的突变会导致散发性和家族性佩吉特骨病。[RefSeq 提供,2009 年 3 月]

This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B (NF-kB) signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone. [provided by RefSeq, Mar 2009]

SQSTM1 基因产物(3)

mRNA Protein Name
NM_001142298.2 NP_001135770.1 sequestosome-1 isoform 2
NM_001142299.2 NP_001135771.1 sequestosome-1 isoform 2
NM_003900.5 NP_003891.1 sequestosome-1 isoform 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 K63-linked polyubiquitin modification-dependent protein binding IDA
IDA: 通过直接分析推断
28404643 GOA
enables SH2 domain binding IDA
IDA: 通过直接分析推断
8650207 GOA
enables enzyme binding IPI
IPI: 通过物理相互作用推断
27368102 GOA
enables identical protein binding IPI
IPI: 通过物理相互作用推断
16169070 GOA
enables molecular condensate scaffold activity IDA
IDA: 通过直接分析推断
29343546 GOA
enables molecular sequestering activity IDA
IDA: 通过直接分析推断
31281713 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
8618896 GOA
enables protein kinase C binding IPI
IPI: 通过物理相互作用推断
14676191 GOA
enables protein kinase binding IDA
IDA: 通过直接分析推断
8650207 GOA
enables protein sequestering activity IDA
IDA: 通过直接分析推断
37306101 GOA
enables protein-macromolecule adaptor activity IDA
IDA: 通过直接分析推断
26344566 GOA
enables signaling receptor activity IDA
IDA: 通过直接分析推断
28871090 GOA
enables ubiquitin binding IDA
IDA: 通过直接分析推断
12857745 GOA
enables ubiquitin protein ligase binding IDA
IDA: 通过直接分析推断
27368102 GOA
enables ubiquitin protein ligase binding IPI
IPI: 通过物理相互作用推断
25127057 GOA
enables ubiquitin-modified protein reader activity IDA
IDA: 通过直接分析推断
22017874 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in aggrephagy IDA
IDA: 通过直接分析推断
17580304 GOA
involved in aggrephagy IPI
IPI: 通过物理相互作用推断
28404643 GOA
involved in autophagy IDA
IDA: 通过直接分析推断
20452972 GOA
involved in autophagy IMP
IMP: 通过突变表型推断
17580304 GOA
involved in cellular response to stress IDA
IDA: 通过直接分析推断
17580304 GOA
involved in endosome organization IDA
IDA: 通过直接分析推断
27368102 GOA
involved in macroautophagy IMP
IMP: 通过突变表型推断
20168092 GOA
involved in mitophagy IGI
IGI: 通过遗传相互作用推断
20457763 GOA
involved in negative regulation of ferroptosis IMP
IMP: 通过突变表型推断
26403645 GOA
involved in negative regulation of protein ubiquitination IDA
IDA: 通过直接分析推断
20452972 GOA
involved in negative regulation of toll-like receptor 4 signaling pathway IDA
IDA: 通过直接分析推断
31281713 GOA
involved in non-membrane-bounded organelle assembly IDA
IDA: 通过直接分析推断
29343546 GOA
involved in pexophagy IDA
IDA: 通过直接分析推断
26344566 GOA
involved in positive regulation of autophagy IDA
IDA: 通过直接分析推断
28871090 GOA
involved in protein catabolic process IDA
IDA: 通过直接分析推断
27498865 GOA
involved in protein localization to perinuclear region of cytoplasm IDA
IDA: 通过直接分析推断
27368102 GOA
involved in protein targeting to vacuole involved in autophagy IDA
IDA: 通过直接分析推断
27498865 GOA
involved in regulation of canonical NF-kappaB signal transduction IMP
IMP: 通过突变表型推断
12857745 GOA
involved in regulation of protein complex stability IDA
IDA: 通过直接分析推断
25127057 GOA
involved in response to mitochondrial depolarisation IGI
IGI: 通过遗传相互作用推断
20457763 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in P-body IDA
IDA: 通过直接分析推断
20357094 GOA
located in PML body IDA
IDA: 通过直接分析推断
20168092 GOA
located in amphisome IDA
IDA: 通过直接分析推断
19640926 GOA
located in autolysosome IDA
IDA: 通过直接分析推断
19640926 GOA
is active in autophagosome IDA
IDA: 通过直接分析推断
30612879 GOA
located in autophagosome IDA
IDA: 通过直接分析推断
17580304 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
20168092 GOA
is active in cytosol IDA
IDA: 通过直接分析推断
8650207 GOA
located in inclusion body IDA
IDA: 通过直接分析推断
20168092 GOA
is active in intracellular non-membrane-bounded organelle IDA
IDA: 通过直接分析推断
22017874 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

SQSTM1 蛋白结构

PB1

PB1: PB1 domain (41 - 100)

ZZ

ZZ: Zinc finger, ZZ type (123 - 158)

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

sequestosome-1

EBI3-associated protein of 60 kDa

SQSTM1 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
SQSTM1 Q13501 NTRK1 Homo sapiens P04629 17389358
种属内
SQSTM1 Q13501 MALT1 Homo sapiens Q9UDY8 16874300
种属内
SQSTM1 Q13501 MALT1 Homo sapiens Q9UDY8 16874300
种属内
SQSTM1 Q13501 HSPA1A Homo sapiens P0DMV8 32814053
种属内
SQSTM1 Q13501 HSPA1A Homo sapiens P0DMV8 32814053
种属内
SQSTM1 Q13501 HSPA1A Homo sapiens P0DMV8 32814053
种属内
SQSTM1 Q13501 MAP1LC3C Homo sapiens Q9BXW4 19250911
种属内
SQSTM1 Q13501 MAP1LC3C Homo sapiens Q9BXW4
FPS
33436498
种属内
SQSTM1 Q13501 MAP1LC3C Homo sapiens Q9BXW4 20562859
种属间
SQSTM1 Q13501 ATG8 Saccharomyces cerevisiae P38182 19250911
种属间
SQSTM1 Q13501 ATG8 Saccharomyces cerevisiae P38182
Y2H
19250911
种属内
SQSTM1 Q13501 CNR2 Homo sapiens P34972 31616248
种属内
SQSTM1 Q13501 CNR2 Homo sapiens P34972 31616248
种属内
SQSTM1 Q13501 PRKCI Homo sapiens P41743 20808283
种属内
SQSTM1 Q13501 PRKCI Homo sapiens P41743 20562859
种属内
SQSTM1 Q13501 PRKCI Homo sapiens P41743 34524948
种属内
SQSTM1 Q13501 VDR Homo sapiens P11473 27728806
种属内
SQSTM1 Q13501 CDC37 Homo sapiens Q16543 32296183
种属内
SQSTM1 Q13501 CDC37 Homo sapiens Q16543 20562859
种属内
SQSTM1 Q13501 MAP1LC3B Homo sapiens Q9GZQ8
Y2H
19250911
种属内
SQSTM1 Q13501 NIPSNAP1 Homo sapiens Q9BPW8 34524948
种属内
SQSTM1 Q13501 NIPSNAP1 Homo sapiens Q9BPW8 35271311
种属内
SQSTM1 Q13501 NIPSNAP1 Homo sapiens Q9BPW8 20562859
种属内
SQSTM1 Q13501 MAP2K5 Homo sapiens Q13163 32296183
种属内
SQSTM1 Q13501 UBC Homo sapiens P0CG48
Y2H
8702753
种属内
SQSTM1 Q13501 UBC Homo sapiens P0CG48
Y2H
21900206
种属内
SQSTM1 Q13501 SH3KBP1 Homo sapiens Q96B97 20551902
种属内
SQSTM1 Q13501 SH3KBP1 Homo sapiens Q96B97 20551902
种属内
SQSTM1 Q13501 SMAD3 Homo sapiens P84022 21988832
种属内
SQSTM1 Q13501 PTPN13 Homo sapiens Q12923 24316673
种属内
SQSTM1 Q13501 TRAF6 Homo sapiens Q9Y4K3 17389358
种属内
SQSTM1 Q13501 SESN2 Homo sapiens P58004 25040165
种属内
SQSTM1 Q13501 LRRK2 Homo sapiens Q5S007
PLA
29519959
种属内
SQSTM1 Q13501 FHOD3 Homo sapiens Q2V2M9-4 21149568
种属内
SQSTM1 Q13501 FHOD3 Homo sapiens Q2V2M9-4
Y2H
21149568
种属内
SQSTM1 Q13501 FHOD3 Homo sapiens Q2V2M9 21149568
种属内
SQSTM1 Q13501 FHOD3 Homo sapiens Q2V2M9 21149568
种属内
SQSTM1 Q13501 GABARAP Homo sapiens O95166 32296183
种属内
SQSTM1 Q13501 GABARAP Homo sapiens O95166 20562859
种属内
SQSTM1 Q13501 GABARAP Homo sapiens O95166 32296183
种属内
SQSTM1 Q13501 GABARAP Homo sapiens O95166
FPS
33436498
种属内
SQSTM1 Q13501 GABARAP Homo sapiens O95166 19250911
种属内
SQSTM1 Q13501 GABARAPL2 Homo sapiens P60520 19250911
种属内
SQSTM1 Q13501 GABARAPL2 Homo sapiens P60520 25416956
种属内
SQSTM1 Q13501 GABARAPL2 Homo sapiens P60520
FPS
33436498
种属内
SQSTM1 Q13501 GABARAPL2 Homo sapiens P60520 20562859
种属内
SQSTM1 Q13501 GABARAPL2 Homo sapiens P60520 25416956
种属内
SQSTM1 Q13501 GABARAPL2 Homo sapiens P60520 16189514
种属内
SQSTM1 Q13501 GABARAPL2 Homo sapiens P60520
Y2H
19250911
种属内
SQSTM1 Q13501 MAP1LC3A Homo sapiens Q9H492 32296183
种属内
SQSTM1 Q13501 MAP1LC3A Homo sapiens Q9H492 19250911
种属内
SQSTM1 Q13501 MAP1LC3A Homo sapiens Q9H492
FPS
33436498
种属内
SQSTM1 Q13501 MAP1LC3A Homo sapiens Q9H492
IF
19427866
种属内
SQSTM1 Q13501 DAZAP2 Homo sapiens Q15038 32296183
种属内
SQSTM1 Q13501 NBR1 Homo sapiens Q14596 19250911
种属内
SQSTM1 Q13501 NBR1 Homo sapiens Q14596 20808283
种属内
SQSTM1 Q13501 NBR1 Homo sapiens Q14596 24879152
种属内
SQSTM1 Q13501 NBR1 Homo sapiens Q14596 19250911
种属内
SQSTM1 Q13501 NBR1 Homo sapiens Q14596 20562859
种属内
SQSTM1 Q13501 RAD23A Homo sapiens P54725 31515488
种属内
SQSTM1 Q13501 GABARAPL1 Homo sapiens Q9H0R8 25416956
种属内
SQSTM1 Q13501 GABARAPL1 Homo sapiens Q9H0R8 20562859
种属内
SQSTM1 Q13501 GABARAPL1 Homo sapiens Q9H0R8 32296183
种属内
SQSTM1 Q13501 GABARAPL1 Homo sapiens Q9H0R8 25416956
种属内
SQSTM1 Q13501 GABARAPL1 Homo sapiens Q9H0R8 16189514
种属内
SQSTM1 Q13501 GABARAPL1 Homo sapiens Q9H0R8 19250911
种属内
SQSTM1 Q13501 GABARAPL1 Homo sapiens Q9H0R8 25416956
种属内
SQSTM1 Q13501 OPTN Homo sapiens Q96CV9 25026213
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 32296183
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 25416956
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 25416956
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 32296183
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 25910212
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 20562859
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 25910212
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 32296183
种属内
SQSTM1 Q13501 KEAP1 Homo sapiens Q14145 25910212
种属内
SQSTM1 Q13501 CLDN2 Homo sapiens P57739
PLA
37460613
种属内
SQSTM1 Q13501 CLDN2 Homo sapiens P57739
IF
37460613
种属内
SQSTM1 Q13501 IKBKG Homo sapiens Q9Y6K9 16874300
种属内
SQSTM1 Q13501 IKBKG Homo sapiens Q9Y6K9 16874300
种属间
SQSTM1 Q13501 Ulk1 Mus musculus O70405 25040165
种属间: 跨种属相互作用 种属内: 同种属相互作用

SQSTM1 抗体

目录号 产品名 应用 反应物种
HY-P80899 SQSTM1/p62 Antibody (YA062) WB, IHC-F, IHC-P, ICC/IF, IP Human, Mouse

关联疾病

疾病名称 别名
Paget Disease Of Bone 3

PDB3

Osteitis Deformans

Paget Disease Of Bone, Type 3

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3

FTDALS3

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-3

Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 3

Neurodegeneration With Ataxia, Dystonia, And Gaze Palsy, Childhood-Onset

NADGP

Myopathy, Distal, With Rimmed Vacuoles

DMRV

Multisystem Proteinopathy 4

Msp4

Nonaka Myopathy

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1

FTDALS1

Frontotemporal Dementia And/Or Motor Neuron Disease

Ftdmnd

Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia

Alsftd

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1

Frontotemporal Dementia With Motor Neuron Disease

Ftdals

Ftd-Als

Ftd-Mnd

Frontotemporal Dementia With Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1

Amyotrophic Lateral Sclerosis/Frontotemporal Dementia

Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1

Frontotemporal Lobar Degeneration

Grn-Related Frontotemporal Dementia

Paget'S Disease Of Bone

Osteitis Deformans

Paget Disease Of Bone

Osseous Paget'S Disease

Paget Disease Of Bone, Familial

Bone Paget Disease

Familial Paget'S Disease Of Bone

Paget'S Bone Disease

Familial Paget Disease Of Bone

Paget Disease, Bone

Pdb

Pagets Bone Disease

Spastic Paraplegia-Paget Disease Of Bone Syndrome
Paget Disease Of Bone 2, Early-Onset

PDB2

Paget Disease Of Bone, Type 2, Early-Onset

Pick Disease Of Brain

Pick Disease

Pick'S Disease

Pick Disease Of The Brain

Lobar Atrophy Of Brain

Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions

Behavioral Variant Of Frontotemporal Dementia

Dementia In Pick'S Disease

Lobar Atrophy Of The Brain

Bvftd

Bv-Ftd

PIDB

Picks Disease

Amyotrophic Lateral Sclerosis 1

Amyotrophic Lateral Sclerosis

ALS

Lou Gehrig Disease

Amyotrophic Lateral Sclerosis Type 1

Charcot Disease

ALS1

Amyotrophic Lateral Sclerosis, Susceptibility To

Fals

Lou Gehrig'S Disease

Mnd

Motor Neuron Disease

Familial Amyotrophic Lateral Sclerosis

Amyotrophic Lateral Sclerosis 1, Familial

Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

Motor Neuron Disease, Bulbar

Motor Neurone Disease

Amyotrophic Lateral Sclerosis With Dementia

Dementia With Amyotrophic Lateral Sclerosis

Motor Neuron Disease, Amyotrophic Lateral Sclerosis

Sclerosis, Lateral, Amyotrophic

Sclerosis, Lateral, Amyotrophic, Type 1

Amyotrophic Sclerosis

Als - [Amyotrophic Lateral Sclerosis]

Wasting Palsy

Amyotrophic Paralysis

Amyotrophy Lateral Sclerosis

Wasting Paralysis

Spinal Progressive Amyotrophy

Progressive Atrophic Paralysis

Welander Distal Myopathy

WDM

Muscular Dystrophy, Distal, Late-Onset, Autosomal Dominant

Myopathy, Distal, Swedish

Welander Distal Myopathy, Swedish Type

Distal Myopathy, Swedish Type

Distal Myopathy, Welander Type

Late-Onset Autosomal Dominant Distal Muscular Dystrophy

Swedish Distal Myopathy

Familial Expansile Osteolysis

FEO

Mccabe Disease

Osteolysis, Familial Expansile

Polyostotic Osteolytic Dysplasia, Hereditary Expansile

Hepod

Expansile Osteolysis, Familial

Eof

Hereditary Expansile Polyostotic Osteolytic Dysplasia

Frontotemporal Dementia

Pallidopontonigral Degeneration

Frontotemporal Lobar Degeneration

Semantic Dementia

FTD

Frontotemporal Lobe Dementia

Multiple System Tauopathy With Presenile Dementia

Dementia, Frontotemporal

Frontotemporal Dementia With Parkinsonism

Mstd

Frontotemporal Lobar Degeneration With Tau Inclusions

Ftld With Tau Inclusions

Dementia, Frontotemporal, With Parkinsonism

Fldem

Ftdp17

Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

Ddpac

Wilhelmsen-Lynch Disease

Wld

Ppnd

Dementia, Frontotemporal, With Or Without Parkinsonism

Semantic Primary Progressive Aphasia

Semantic Variant Ppa

Wilhemsen-Lynch Disease

Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

Ftd-Als

Ftld

Pick Complex

Pick Disease Of The Brain

Frontotemporal Dementia With Parkinsonism-17

Grn-Related Frontotemporal Dementia

Frontotemporal Dementia With Motor Neuron Disease

Dementia In Fronto-Temporal Lobar Degeneration

Ftd - [Frontotemporal Dementia]

Temple Dementia

Frontal Lobe Dementia

Dementia

Dementias

Presenile Dementia

Alzheimer Type Dementia

Alzheimer Sclerosis

Alzheimer Disease Dementia

Alzheimer Dementia

Primary Degenerative Alzheimer Type Dementia

End Stage Alzheimer'S Dementia

Alzheimer'S Type Atypical Dementia

Alzheimer Type Presenile Dementia

Early Onset Alzheimer Dementia

Dementia In Alzheimer Disease Type 2

Dementia In Alzheimer Disease With Early Onset

Early Onset Alzheimer Type Dementia, Uncomplicated

Primary Degenerative Alzheimer Type Dementia, Early Onset

Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated

Alzheimer Disease Dementia With Early Onset

Presenile Sclerosis

Presenile Brain Sclerosis

Presenile Alzheimer Brain Sclerosis

Late Onset Alzheimer Dementia

Dementia In Alzheimer Disease Type 1

Dementia In Alzheimer Disease With Late Onset

Primary Degenerative Alzheimer Type Dementia, Late Onset

Sdat - [Senile Dementia, Alzheimer Type]

Alzheimer Disease Dementia With Late Onset

Late Onset Alzheimer Brain Sclerosis

Senile Alzheimer Brain Disease

Senile Alzheimer Brain Sclerosis

Senile Primary Degenerative Alzheimer Type Dementia

Senile Dementia Of The Alzheimer Type

Arteriosclerotic Dementia

Strategic-Infarct Dementia

Post Stroke Dementia

Vascular Cognitive Impairment

Vascular Dementia

Dementia Of The Lewy Body Type

Dementia With Lewy Bodies

Sdlt - [Senile Dementia Of The Lewy Body Type]

Senile Dementia Of The Lewy Body Type

Alcohol-Related Dementia

Alcoholic Dementia Nos

Alcohol-Induced Dementia

Alcoholic Brain Syndrome

Chronic Alcoholic Brain Syndrome

Alcohol Dementia

Late Onset Alcoholic Psychosis

Residual And Late-Onset Alcohol-Induced Psychotic Disorder

Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder

Late-Onset Psychoactive Substance-Induced Psychotic Disorder

Inhalant Dementia

Volatile Solvents Dementia

Dementia In Paralysis Agitans

Pdd - [Parkinson Disease Dementia]

Dementia Syndrome Of Parkinson Disease

Dementia In Parkinson Disease

Parkinson Related Dementia

Dementia In Huntington Chorea

Hiv - [Human Immunodeficiency Virus] Dementia

Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex

Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex

Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex

Aids Related Dementia

Dementia Due To Niacin Deficiency

Amyotrophic Lateral Sclerosis 3

ALS3

Amyotrophic Lateral Sclerosis Type 3

Motor Neuron Disease

Anterior Horn Cell Disease

Motor Neuron Diseases

Mnd - [Motor Neurone Disease]

Lou Gehrig Disease

Creeping Palsy

Creeping Paralysis

Bulbar Motor Neuron Disease

Bulbar Syndrome

Anterior Horn Cell Disorder

Hereditary Motor Neuron Disease

Huntington Disease

Huntington'S Disease

Huntington Chorea

Huntington'S Chorea

HD

Huntington Chronic Progressive Hereditary Chorea

Juvenile Huntington Disease

Chronic Progressive Chorea

Chronic Progressive Hereditary Chorea

Hc - [Huntington Chorea]

Hereditary Chorea

Progressive Hereditary Chorea

Cystinosis

Cystine Storage Disease

Cystine Diathesis

Cystine Disease

Cystinoses

Protein Defect Of Cystin Transport

Cystin Transport, Protein Defect Of

Nephropathic Cystinosis

Protein Defect Of Cystine Transport

Lateral Sclerosis

Primary Lateral Sclerosis

Adult-Onset Primary Lateral Sclerosis

Adult-Onset Pls

Motor Neuron Disease

Pls

Pls - [Primary Lateral Sclerosis]

Lateral Spinal Sclerosis

Lateral Complete Paralysis

Lateral Incomplete Paralysis

Lateral Paralysis

Multiple System Atrophy 1

Multiple System Atrophy

Shy-Drager Syndrome

Msa

MSA1

Multiple System Atrophy 1, Susceptibility To

Sporadic Olivopontocerebellar Atrophy

Multisystem Atrophy

Msa1, Susceptibility To

Multiple System Atrophy, Susceptibility To

Opca

Progressive Autonomic Failure With Multiple System Atrophy

Sds

Periostitis
Machado-Joseph Disease

SCA3

MJD

Spinocerebellar Ataxia 3

Azorean Disease

Spinocerebellar Ataxia Type 3

Spinocerebellar Atrophy

Azorean Neurologic Disease

Spinopontine Atrophy

Nigrospinodentatal Degeneration

Spinocerebellar Atrophy Iii

Spinocerebellar Atrophy Type 3

Azorean Ataxia

Azorean Disease Of The Nervous System

Machado Disease

Nigro-Spino-Dentatal Degeneration With Nuclear Ophthalmoplegia

Disease, Machado-Joseph

Ataxia, Spinocerebellar

Dystonia

Dystonic Disease

Dystonic Disorder

Dystonia Disorders

Neuroleptic Dyskinesia

Multisystem Proteinopathy
Pilocytic Astrocytoma

Juvenile Pilocytic Astrocytoma

Grade I Astrocytic Tumor

Piloid Astrocytoma

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

Mammary Paget'S Disease

Paget'S Disease

Mammary Paget Disease

Paget'S Disease Of The Breast

Paget Disease Of The Breast

Paget'S Disease Of The Nipple

Paget'S Disease, Mammary

Paget Cell Neoplasm

Paget Disease Of The Nipple

Pagets Disease Mammary

Osteitis Deformans

Myopathy

Muscular Diseases

Myopathies

Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia

Ibmpfd

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia

Pagetoid Amyotrophic Lateral Sclerosis

Pagetoid Neuroskeletal Syndrome

Inclusion Body Myopathy With Paget Disease Of Bone And/Or Frontotemporal Dementia

Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone And/Or Frontotemporal Dementia

Multisystem Proteinopathy

Limb-Girdle Muscular Dystrophy With Paget Disease Of Bone

Inclusion Body Myopathy With Paget'S Disease Of Bone And Frontotemporal Dementia

Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dement

Lower Motor Neuron Degeneration With Paget-Like Bone Disease

Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone

Myopathy, Inclusion Body, With Early-Onset Paget Disease And Frontotemporal Dementia

Alcoholic Hepatitis

Acute Alcoholic Hepatitis

Acute Alcoholic Liver Disease

Hepatitis, Alcoholic

Hepatitis Alcoholic

Ah - [Alcoholic Hepatitis]

Ethanol Hepatitis

Muscular Atrophy

Muscle Wasting

Amyotrophia

Wasting - Muscle

Skeletal Muscle Atrophy

Parkinson Disease, Late-Onset

Parkinson Disease

Parkinson'S Disease

PD

PARK

Parkinson Disease, Susceptibility To

Late Onset Parkinson'S Disease

Late Onset Parkinson Disease

Paralysis Agitans

Primary Parkinsonism

Idiopathic Parkinson Disease

Parkinson'S

Parkinson Disease, Late-Onset, Susceptibility To

Parkinson Disease, Age Of Onset, Modifier

Lewy Body Parkinson Disease

Idiopathic Parkinson'S Disease

Pd - [Parkinson Disease]

Parkinson Disease Nos

Parkinson, Nos

Primary Parkinson Disease

Spinocerebellar Ataxia, Autosomal Recessive 20

Autosomal Recessive Spinocerebellar Ataxia 20

SCAR20

Intellectual Disability-Coarse Face-Macrocephaly-Cerebellar Hypotrophy Syndrome

Autosomal Recessive Spinocerebellar Ataxia Type 20

Intellectual Disability-Coarse Face-Macrocephaly-Cerebellar Hypoplasia Syndrome

Spinocerebellar Ataxia, Autosomal Recessive, 20

Ataxia, Spinocerebellar, Autosomal Recessive, Type 20

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

Myopathy, X-Linked, With Excessive Autophagy

X-Linked Myopathy With Excessive Autophagy

Xmea

MEAX

Vacuolar Myopathy

Nonaka Myopathy

Gne Myopathy

Hibm

Distal Myopathy With Rimmed Vacuoles

Hereditary Inclusion Body Myopathy

Ibm2

Inclusion Body Myopathy, Quadriceps-Sparing

Qsm

Dmrv

Distal Myopathy, Nonaka Type

Inclusion Body Myopathy 2

Inclusion Body Myopathy, Autosomal Recessive

NM

Nonaka Distal Myopathy

Myopathy, Distal, With Or Without Rimmed Vacuoles

Inclusion Body Myopathy, Hereditary, Autosomal Recessive

Inclusion Body Myopathy Type 2

Quadriceps-Sparing Myopathy

Quadriceps Sparing Myopathy

Rimmed Vacuole Myopathy

Inclusion Body Myopathy 2, Autosomal Recessive, Formerly

Ibm2, Formerly

Hibm2

Hereditary Inclusion Body Myopathy Type 2

Inclusion Body Myopathy 2, Autosomal Recessive

Myopathy, Distal, With Rimmed Vacuoles

Inclusion Body Myopathy Autosomal Recessive

Myopathy, Inclusion Body, Type 2

Myopathy, Nonaka

Breast Adenocarcinoma

Mammary Adenocarcinoma

Adenocarcinoma Of Breast

Danon Disease

Pseudoglycogenosis Ii

Antopol Disease

Glycogen Storage Disease Iib

Glycogen Storage Disease Type 2b

Glycogen Storage Disease Type Iib

Gsd2b

Lysosomal Glycogen Storage Disease Without Acid Maltase Deficiency

Vacuolar Cardiomyopathy And Myopathy X-Linked

Vacuolar Cardiomyopathy And Myopathy, X-Linked

Lysosomal Glycogen Storage Disease Without Acid Maltase Deficiency, Formerly

Gsd2b, Formerly

Gsd Iib, Formerly

Glycogen Storage Cardiomyopathy

Glycogen Storage Disease Limited To The Heart

Pseudoglycogenosis 2

X-Linked Vacuolar Cardiomyopathy And Myopathy

Lysosomal Glycogen Storage Disease With Normal Acid Maltase

Glycogen Storage Disease Due To Lamp-2 Deficiency

Gsd Due To Lamp-2 Deficiency

Glycogenosis Due To Lamp-2 Deficiency

Lysosomal Glycogen Storage Disease With Normal Acid Maltase Activity

DAND

Gsd-Iib

Charcot-Marie-Tooth Disease, Axonal, Type 2e

Charcot-Marie-Tooth Disease Type 2

CMT2E

CMT2S

CMT2Y

Charcot-Marie-Tooth Disease Type 2e

Charcot-Marie-Tooth Disease Type 2y

Charcot-Marie-Tooth Disease Axonal Type 2s

Charcot-Marie-Tooth Disease, Axonal, Type 2s

Charcot-Marie-Tooth Disease, Type 2e

Hereditary Motor And Sensory Neuropathy Type 2

Charcot-Marie-Tooth Neuropathy, Type 2s

Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s

Charcot-Marie-Tooth Disease, Axonal, Type 2y

Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y

Charcot-Marie-Tooth Neuropathy, Type 2y

Charcot-Marie-Tooth Disease, Type 2y

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e

Charcot-Marie-Tooth Neuropathy Type 2e

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation

Cmt2 Due To Vcp Mutation

Charcot-Marie-Tooth Disease Type 2s

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2

Autosomal Dominant Axonal Charcot-Marie-Tooth Disease

Cmt2

Charcot-Marie-Tooth Neuropathy, Type 2e

Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type

Hereditary Motor And Sensory Neuropathy Okinawa Type

Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y

Charcot-Marie-Tooth Neuropathy Type 2y

Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s

Charcot-Marie-Tooth Neuropathy Type 2s

Charcot-Marie-Tooth Type 2

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y

Charcot-Marie-Tooth Disease 2e

Charcot-Marie-Tooth Disease Axonal Type 2e

Charcot-Marie-Tooth Disease Neuronal Type 2e

Charcot-Marie-Tooth Disease 2s

Charcot-Marie-Tooth Neuropathy Axonal Type 2s

Charcot-Marie-Tooth Disease 2y

Charcot-Marie-Tooth Disease, Type 2

Hereditary Motor And Sensory-Neuropathy Type Ii

Diamond-Blackfan Anemia 20

DBA20

Rps15a-Related Diamond-Blackfan Anemia

Macular Degeneration, Age-Related, 14

Age Related Macular Degeneration 14

ARMD14

Macular Degeneration, Age-Related, 14, Reduced Risk Of

Macular Degeneration, Age-Related, Type 14

Beach Ear

Acute Swimmer'S Ear

Acute Bacterial Inflammation Of External Ear

Acute Otitis Externa, Diffuse

Acute Swimmers' Ear

Tank Ear

Liver Carcinoma In Situ

Carcinoma In Situ Of Liver And Biliary System

Carcinoma In Situ Of Liver, Gallbladder And Bile Ducts

Pheochromocytoma

Pheochromocytoma, Susceptibility To

Phaeochromocytoma

Adrenal Gland Chromaffin Paraganglioma

Adrenal Gland Chromaffinoma

Adrenal Gland Paraganglioma

Adrenal Gland Pheochromocytoma

Chromaffin Paraganglioma Of The Adrenal Gland

Intraadrenal Paraganglioma

PCC

Chromaffin Cell Tumor

Medullary Chromaffinoma

Medullary Paraganglioma

Pheochromoblastoma

Pheochromocytomas

Chromaffin Cell Neoplasm

Pheochromocytoma, Malignant

Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone With Or Without Frontotemporal Dementia 2

Ibmpfd2

Msp2

Multisystem Proteinopathy 2

Neuronal Ceroid Lipofuscinosis

Hereditary Ceroid Lipofuscinosis

Batten Disease

Ncl

Neuronal Ceroid-Lipofuscinoses

Lipofuscinosis, Ceroid, Neuronal

Juvenile Neuronal Ceroid Lipofuscinosis

Cerebromacular Dystrophy

Cerebromacular Degeneration

Ceroid-Lipofuscinosis

Ncl - [Neuronal Ceroid Lipofuscinosis]

Amaurotic Familial Idiocy

Amaurotic Idiocy

Amaurotic Idiot

Neuronal Lipofuscinosis

Pigmentary Retinal Lipoid Neuronal Heredodegeneration

Myofibrillar Myopathy

Desmin Related Myopathy

Myotilinopathy

Myopathy, Myofibrillar

Alpha Beta Crystallinopathy

Desmin Storage Myopathy

Desminopathy

Filaminopathy

Protein Surplus Myopathy

Zaspopathy

Myofibrillar Myopathies

Myopathy, Myofibrillar, Desmin-Related

Myopathy, Desmin Storage

Mfm - [Myofibrillar Myopathy]

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

Dementia, Lewy Body

Lewy Body Dementia

Lewy Body Disease

Diffuse Lewy Body Disease

Dementia With Lewy Bodies

DLB

Autosomal Dominant Diffuse Lewy Body Disease

Cortical Lewy Body Disease

Dementia, Lewy Body, Susceptibility To

Lewy Body Dementia, Susceptibility To

Senile Dementia Of The Lewy Body Type

Dementia Of The Lewy Body Type

Lbd

Diffuse Lewy Body Disease With Gaze Palsy

Dysphasic Dementia Hereditary

Lewy Body Type Senile Dementia

Lewy Body Variant Of Alzheimer Disease

Lewy Bodies

Lewy Body

Dlbd - [Diffuse Lewy Body Disease]

Clbd - [Cortical Lewy Body Disease]

Alzheimer Disease, Familial, 1

Alzheimer Disease

Alzheimer'S Disease

Presenile And Senile Dementia

AD1

Alzheimer Disease, Susceptibility To

Alzheimer Disease, Late-Onset, Susceptibility To

Alzheimer Disease 1, Familial

AD

Familial Alzheimer Disease

Alzheimer Disease, Late-Onset

Alzheimers Dementia

Alzheimer Dementia

Alzheimer Sclerosis

Alzheimer Syndrome

Alzheimer-Type Dementia

Dat

Primary Senile Degenerative Dementia

Sdat

Alzheimer Disease 1

Autosomal Dominant Alzheimer Disease

Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

Late Onset Alzheimer Disease

Alzheimers Disease

Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

Late-Onset Alzheimers Disease

Alzheimer'S Disease Pathway Kegg

Dementia Due To Alzheimer'S Disease

Alzheimer Disease Type 1

Alzheimers

Hereditary Spastic Paraplegia

Familial Spastic Paraplegia

Hereditary Spastic Paraparesis

Strumpell-Lorrain Disease

Familial Spastic Paraparesis

Hsp

Spg

Strümpell-Lorrain Disease

Spastic Paraplegia, Hereditary

French Settlement Disease

Strumpell-Lorrain Syndrome

Fsp

Spastic Paraplegia, Familial

Spastic Paraplegia Hereditary

Spastic Paraplegia 3, Autosomal Dominant

Spastic Paraparesis

Hereditary Spastic Paralysis

Familial Spastic Paralysis

Hereditary Spastic Ataxia

Nervous System Disease

Abnormality Of The Nervous System

Nervous System Diseases

Nervous System Disorder

Peripheral Nervous System Disease

Peripheral Neuropathy

Peripheral Nerve Disease

Peripheral Nerve Disorders

Neuropathy, Peripheral

Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

Charcot-Marie-Tooth Disease

Cmt

Hmsn

Hereditary Motor And Sensory Neuropathy

Pma

Cmt - Charcot-Marie-Tooth Disease

Charcot Marie Tooth Disease

Charcot-Marie-Tooth Hereditary Neuropathy

Charcot-Marie-Tooth Syndrome

Peroneal Muscular Atrophy

Hereditary Motor And Sensory Neuropathies

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
Felis catus SQSTM1 VGNC VGNC:65669
Rattus norvegicus SQSTM1 RGD RGD:69287
Mus musculus SQSTM1 MGD MGI:107931
Canis familiaris SQSTM1 VGNC VGNC:46787
Macaca mulatta SQSTM1 VGNC VGNC:77876
Bos taurus SQSTM1 VGNC VGNC:35265