1. Gene
  2. HDAC6 - histone deacetylase 6 Gene

HDAC6 - histone deacetylase 6 Gene

中文名称:组蛋白脱乙酰酶 6

种属: Homo sapiens

同用名: HD6; JM21; CPBHM; PPP1R90

基因 ID: 10013 | 基因类型: protein coding

关于 HDAC6

Cytogenetic location: Xp11.23 Genomic coordinates (GRCh38): X:48,801,398-48,824,982 (from NCBI)

This gene has 84 transcripts (splice variants), 182 orthologues, 10 paralogues and is associated with 2 phenotypes. Ubiquitous expression in kidney (RPKM 18.6), testis (RPKM 15.9) and 25 other tissues.

功能概要

组蛋白在转录调控、细胞周期进程和发育事件中发挥关键作用。组蛋白乙酰化/去乙酰化改变染色体结构并影响转录因子对 DNA 的访问。该基因编码的蛋白质属于组蛋白脱乙酰酶/acuc/apha 家族的 II 类。它包含两个催化结构域的内部重复,这两个催化结构域似乎彼此独立发挥作用。这种蛋白质具有组蛋白脱乙酰酶活性并抑制转录。[RefSeq 提供,2008 年 7 月]

Histones play a critical role in transcriptional regulation, cell cycle progression, and developmental events. Histone acetylation/deacetylation alters chromosome structure and affects transcription factor access to DNA. The protein encoded by this gene belongs to class II of the histone deacetylase/acuc/apha family. It contains an internal duplication of two catalytic domains which appear to function independently of each Other. This protein possesses histone deacetylase activity and represses transcription. [provided by RefSeq, Jul 2008]

HDAC6 基因产物(17)

mRNA Protein Name
XM_047441706.1 XP_047297662.1 histone deacetylase 6 isoform X3
NM_001321225.2 NP_001308154.1 histone deacetylase 6 isoform a
NR_135591.1
NM_001321229.1 NP_001308158.1 histone deacetylase 6 isoform b
XM_047441704.1 XP_047297660.1 histone deacetylase 6 isoform X2
NM_001321226.2 NP_001308155.1 histone deacetylase 6 isoform b
NM_001321231.2 NP_001308160.1 histone deacetylase 6 isoform c
NR_135593.2
XM_047441705.1 XP_047297661.1 histone deacetylase 6 isoform X3
NM_006044.4 NP_006035.2 histone deacetylase 6 isoform b
XR_007068179.1
NM_001321227.2 NP_001308156.1 histone deacetylase 6 isoform b
NM_001321228.2 NP_001308157.1 histone deacetylase 6 isoform b
XM_047441703.1 XP_047297659.1 histone deacetylase 6 isoform X1
NM_001321230.2 NP_001308159.1 histone deacetylase 6 isoform c
XM_047441707.1 XP_047297663.1 histone deacetylase 6 isoform X4
NR_135592.2
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 Hsp90 protein binding IDA
IDA: 通过直接分析推断
15916966 GOA
enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA
IDA: 通过直接分析推断
24413532 GOA
NOT enables acetylspermidine deacetylase activity IDA
IDA: 通过直接分析推断
28516954 GOA
enables alpha-tubulin binding IDA
IDA: 通过直接分析推断
19228685 GOA
enables beta-catenin binding IPI
IPI: 通过物理相互作用推断
18356165 GOA
enables dynein complex binding IDA
IDA: 通过直接分析推断
14675537 GOA
enables histone deacetylase activity IDA
IDA: 通过直接分析推断
10220385 GOA
enables histone deacetylase activity IMP
IMP: 通过突变表型推断
23322205 GOA
enables histone deacetylase binding IPI
IPI: 通过物理相互作用推断
12620231 GOA
enables microtubule binding IDA
IDA: 通过直接分析推断
19228685 GOA
enables misfolded protein binding EXP
EXP: 通过实验结果推断
17785525 GOA
enables polyubiquitin modification-dependent protein binding IDA
IDA: 通过直接分析推断
14675537 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
16919237 GOA
enables protein lysine deacetylase activity IDA
IDA: 通过直接分析推断
28516954 GOA
enables tau protein binding IDA
IDA: 通过直接分析推断
18636984 GOA
enables transcription corepressor binding IPI
IPI: 通过物理相互作用推断
12535528 GOA
enables tubulin deacetylase activity EXP
EXP: 通过实验结果推断
12024216 GOA
enables tubulin deacetylase activity IDA
IDA: 通过直接分析推断
12620231 GOA
enables tubulin deacetylase activity IMP
IMP: 通过突变表型推断
19457097 GOA
enables ubiquitin protein ligase binding IPI
IPI: 通过物理相互作用推断
21753002 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in aggresome assembly IMP
IMP: 通过突变表型推断
14675537 GOA
involved in axonal transport of mitochondrion IGI
IGI: 通过遗传相互作用推断
28105056 GOA
involved in cellular response to hydrogen peroxide IMP
IMP: 通过突变表型推断
18606987 GOA
involved in cellular response to topologically incorrect protein IMP
IMP: 通过突变表型推断
16192271 GOA
involved in cilium disassembly IDA
IDA: 通过直接分析推断
26246421 GOA
involved in cilium disassembly IMP
IMP: 通过突变表型推断
17604723 GOA
involved in intracellular protein transport IMP
IMP: 通过突变表型推断
16192271 GOA
involved in lysosome localization IMP
IMP: 通过突变表型推断
16192271 GOA
involved in negative regulation of aggrephagy IDA
IDA: 通过直接分析推断
31857589 GOA
involved in negative regulation of gene expression, epigenetic IMP
IMP: 通过突变表型推断
24413532 GOA
involved in negative regulation of protein-containing complex assembly IMP
IMP: 通过突变表型推断
23962722 GOA
involved in negative regulation of protein-containing complex disassembly IMP
IMP: 通过突变表型推断
15916966 GOA
involved in negative regulation of proteolysis IMP
IMP: 通过突变表型推断
18356165 GOA
involved in peptidyl-lysine deacetylation IMP
IMP: 通过突变表型推断
18356165 GOA
NOT involved in polyamine deacetylation IDA
IDA: 通过直接分析推断
28516954 GOA
involved in polyubiquitinated misfolded protein transport IMP
IMP: 通过突变表型推断
14675537 GOA
involved in positive regulation of epithelial cell migration IMP
IMP: 通过突变表型推断
12024216 GOA
involved in positive regulation of peptidyl-serine phosphorylation IMP
IMP: 通过突变表型推断
23962722 GOA
acts upstream of positive regulation of signaling receptor activity IMP
IMP: 通过突变表型推断
15916966 GOA
involved in protein deacetylation IDA
IDA: 通过直接分析推断
28516954 GOA
involved in protein deacetylation IMP
IMP: 通过突变表型推断
15916966 GOA
involved in protein quality control for misfolded or incompletely synthesized proteins IMP
IMP: 通过突变表型推断
14675537 GOA
involved in regulation of macroautophagy IMP
IMP: 通过突变表型推断
16192271 GOA
involved in regulation of protein stability IMP
IMP: 通过突变表型推断
23580651 GOA
involved in response to growth factor IMP
IMP: 通过突变表型推断
18356165 GOA
involved in response to misfolded protein IMP
IMP: 通过突变表型推断
14675537 GOA
NOT involved in spermidine deacetylation IDA
IDA: 通过直接分析推断
28516954 GOA
involved in tubulin deacetylation IDA
IDA: 通过直接分析推断
19228685 GOA
involved in type 2 mitophagy 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 aggresome IDA
IDA: 通过直接分析推断
14675537 GOA
located in caveola IDA
IDA: 通过直接分析推断
18356165 GOA
located in cell leading edge IDA
IDA: 通过直接分析推断
12024216 GOA
located in centrosome IDA
IDA: 通过直接分析推断
26246421 GOA
located in ciliary basal body IDA
IDA: 通过直接分析推断
17604723 GOA
located in cytoplasm IDA
IDA: 通过直接分析推断
24687993 GOA
part of histone deacetylase complex IDA
IDA: 通过直接分析推断
11948178 GOA
located in inclusion body IDA
IDA: 通过直接分析推断
16192271 GOA
located in microtubule IDA
IDA: 通过直接分析推断
12620231 GOA
part of microtubule associated complex IDA
IDA: 通过直接分析推断
19228685 GOA
located in perinuclear region of cytoplasm IDA
IDA: 通过直接分析推断
12024216 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

HDAC6 蛋白结构

Hist_deacetyl

Hist_deacetyl: Histone deacetylase domain (102 - 402)

Hist_deacetyl

Hist_deacetyl: Histone deacetylase domain (496 - 798)

zf-UBP

zf-UBP: Zn-finger in ubiquitin-hydrolases and other protein (1133 - 1193)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1215 a.a.
蛋白主名 其他名称

histone deacetylase 6

protein phosphatase 1, regulatory subunit 90

tubulin-lysine deacetylase HDAC6

HDAC6 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
HDAC6 Q9UBN7 PRKCA Homo sapiens P17252
Anti Tag CoIP
21952047
种属内
HDAC6 Q9UBN7 CYLD Homo sapiens Q9NQC7
Anti Tag CoIP
19893491
种属内
HDAC6 Q9UBN7 CYLD Homo sapiens Q9NQC7
Anti Bait CoIP
19893491
种属内
HDAC6 Q9UBN7 DCTN1 Homo sapiens Q14203-5
Validated Y2H
32814053
种属内
HDAC6 Q9UBN7 DCTN1 Homo sapiens Q14203-5
Y2H Pooling
32814053
种属内
HDAC6 Q9UBN7 DCTN1 Homo sapiens Q14203-5
Y2H Array
32814053
种属内
HDAC6 Q9UBN7 EGFR Homo sapiens P00533
Ub Reconstruction
24658140
种属内
HDAC6 Q9UBN7 EGFR Homo sapiens P00533
Protein Kinase Assay
20029029
种属内
HDAC6 Q9UBN7 EGFR Homo sapiens P00533
Ub Reconstruction
20029029
种属内
HDAC6 Q9UBN7 EGFR Homo sapiens P00533
Anti Tag CoIP
24658140
种属内
HDAC6 Q9UBN7 PROM1 Homo sapiens O43490
Anti Bait CoIP
23084749
种属内
HDAC6 Q9UBN7 PROM1 Homo sapiens O43490
Anti Tag CoIP
23084749
种属间
HDAC6 Q9UBN7 Cttn Mus musculus Q60598
IF
21847094
种属内
HDAC6 Q9UBN7 MYD88 Homo sapiens Q99836
Anti Tag CoIP
29281743
种属内
HDAC6 Q9UBN7 CTNNB1 Homo sapiens P35222
Anti Bait CoIP
18356165
种属内
HDAC6 Q9UBN7 CTNNB1 Homo sapiens P35222
Anti Bait CoIP
23084749
种属内
HDAC6 Q9UBN7 ATP13A2 Homo sapiens Q9NQ11
Ub Reconstruction
22645275
种属内
HDAC6 Q9UBN7 PRKN Homo sapiens O60260
Pull Down
19036992
种属间
HDAC6 Q9UBN7 GRK2 Bos taurus P21146
Pull Down
22193721
种属间
HDAC6 Q9UBN7 GRK2 Bos taurus P21146
Protein Kinase Assay
22193721
种属间
HDAC6 Q9UBN7 Cdc20 Rattus norvegicus Q62623
Anti Tag CoIP
19167333
种属间
HDAC6 Q9UBN7 Cdc20 Rattus norvegicus Q62623
Pull Down
19167333
种属间
HDAC6 Q9UBN7 Tax Human T-cell leukemia virus 1 P03409
Confocal
21532619
种属间
HDAC6 Q9UBN7 Tax Human T-cell leukemia virus 1 P03409
Anti Tag CoIP
21532619
种属间
HDAC6 Q9UBN7 tat Human immunodeficiency virus P04610
Anti Tag CoIP
21220424
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 HDAC6 蛋白

目录号 产品名 蛋白编号 纯度
HY-P72223 HDAC6 Protein, Human (His-SUMO) Q9UBN7-1 (M1-N488) ≥95%
HY-P72224 HDAC6 Protein, Human (His) Q9UBN7-1 (M489-E840) ≥95%

关联疾病

疾病名称 别名
Liver Carcinoma In Situ

Carcinoma In Situ Of Liver And Biliary System

Carcinoma In Situ Of Liver, Gallbladder And Bile Ducts

Mature T-Cell And Nk-Cell Lymphoma

Mature T-Cell And Natural Killer Cell Lymphoma

Nk-T Cell Lymphoma

Atrial Septal Defect 8

ASD8

Atrial Heart Septal Defect 8

Septal Defect, Atrial, Type 8

Alexander Disease

Alexander'S Disease

ALXDRD

Alexanders Leukodystrophy

Axd

Megalencephaly In Infancy Accompanied By Progressive Spasticity And Dementia

Alx

Demyelinogenic Leukodystrophy

Dysmyelinogenic Leukodystrophy

Fibrinoid Degeneration Of Astrocytes

Leukodystrophy With Rosenthal Fibers

Alexander Disease Type Ii

Axd Type Ii

Alexander Disease Type I

Axd Type I

Alexanders Disease

Alexander'S Leukodystrophy

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

Joubert Syndrome 8

JBTS8

Joubert Syndrome, Type 8

Neuromuscular Disease

Neuromuscular Diseases

Neuromuscular Disorders

Neuromuscular Disorder

Spinal And Bulbar Muscular Atrophy, X-Linked 1

Kennedy Disease

Sbma

Spinal And Bulbar Muscular Atrophy

Kennedy'S Disease

X-Linked Spinal And Bulbar Muscular Atrophy

SMAX1

Kd

Kennedy Spinal And Bulbar Muscular Atrophy

Spinobulbar Muscular Atrophy

Bulbospinal Muscular Atrophy, X-Linked

Bulbospinal Neuronopathy, X-Linked Recessive

Xbsn

Spinal And Bulbar Muscular Atrophy Of Kennedy

Bulbospinal Muscular Atrophy

X-Linked Bulbospinal Amyotrophy

Bulbo-Spinal Atrophy, X-Linked

Spinal Bulbar Muscular Atrophy

X-Linked Bulbo-Spinal Atrophy

X-Linked Spinal Bulbar Muscular Atrophy

X-Linked Bsma

X-Linked Bulbospinal Muscular Atrophy

Spinal And Bulbar Muscular Atrophy X-Linked 1

Bulbospinal Muscular Atrophy X-Linked

Bulbospinal Neuronopathy X-Linked Recessive

Kennedy Disease)

Kennedy Syndrome

Atrophy, Muscular, Spinal And Bulbar, Kennedy Type

Atrophy, Muscular, Spinobulbar

Bulbospinal Neuronopathy

Charcot-Marie-Tooth Disease And Deafness

Charcot-Marie-Tooth Disease Type 1e

CMT1E

Charcot-Marie-Tooth Disease Type 1

Charcot-Marie-Tooth Disease, Demyelinating, Type 1e

Hereditary Motor And Sensory Neuropathy Type 1

Charcot-Marie-Tooth Disease, Type I

Charcot-Marie-Tooth Neuropathy And Deafness, Autosomal Dominant

Charcot-Marie-Tooth Disease, Type 1e

Charcot-Marie-Tooth Disease Demyelinating Type 1e

Autosomal Dominant Demyelinating Charcot-Marie-Tooth Disease

Cmt1

Charcot-Marie-Tooth Neuropathy Type 1

Autosomal Dominant Charcot-Marie-Tooth Neuropathy And Deafness

Charcot-Marie-Tooth Disease-Deafness

Charcot-Marie-Tooth Type 1

Hmsn1

Hereditary Motor And Sensory Neuropathy 1

Cmt 1e

Charcot Marie Tooth Disease Type 1e

Charcot-Marie-Tooth Disease-Deafness Syndrome

Charcot-Marie-Tooth Disease-Hearing Loss Syndrome

Charcot-Marie-Tooth Disease 1e

Charcot-Marie-Tooth Disease And Deafness Autosomal Dominant

Charcot-Marie-Tooth Neuropathy Type 1e

Charcot-Marie-Tooth Disease, Type Ie

Hereditary Motor And Sensory Neuropathy Type I

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

Chondrodysplasia With Platyspondyly, Distinctive Brachydactyly, Hydrocephaly, And Microphthalmia

X-Linked Dominant Chondrodysplasia, Chassaing-Lacombe Type

X-Linked Dominant Chondrodysplasia-Hydrocephaly-Microphthalmia Syndrome

CDP-PBHM

Chondrodysplasia, With Platyspondyly, Distinctive Brachydactyly, Hydrocephaly, And Microphthalmia

Peripheral Nervous System Disease

Peripheral Neuropathy

Peripheral Nerve Disease

Peripheral Nerve Disorders

Neuropathy, Peripheral

Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

Autosomal Dominant Polycystic Kidney Disease

Polycystic Kidney Disease, Adult Type

Adpkd

Polycystic Kidney Diseases

Polycystic Kidney, Autosomal Dominant

Congenital Biliary Ectasias

Polycystic Kidney And Hepatic Disease 1

Polycystic Kidney Disease, Autosomal Dominant

Kidney, Polycystic, Disease, Autosomal Dominant

Adult Polycystic Kidney Disease

Polycystic Kidney, Adult Type

Apckd - [Autosomal Polycystic Kidney Disease]

Prolapse Of Urethra

Urethrocele

Rett Syndrome

Atypical Rett Syndrome

RTT

Rts

Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

Rett Syndrome, Atypical

Rett Syndrome, Preserved Speech Variant

Rett'S Disorder

Rett Syndrome Variant

Rett Disorder

Cerebroatrophic Hyperammonemia

Rett Like Syndrome

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

Rett'S Syndrome

Atypical Rtt

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

Rett Syndrome Preserved Speech Variant

Rett Syndrome Zappella Variant

Rett Syndrome, Zappella Variant

B-Cell Lymphoma

Lymphoma, B-Cell

B-Cell Lymphomas

B-Cell Lymphocytic Neoplasm

Lymphoma B-Cell

B-Cell Lymphoma Nos

Nervous System Disease

Abnormality Of The Nervous System

Nervous System Diseases

Nervous System Disorder

Polycystic Kidney Disease

Polycystic Kidney Diseases

Pkd

Polycystic Renal Disease

Kidney Disease, Polycystic

Polycystic Kidney, Autosomal Dominant

Joubert Syndrome 1

Joubert Syndrome

Jbts

Cerebellooculorenal Syndrome 1

JBTS1

Joubert-Boltshauser Syndrome

Cerebelloparenchymal Disorder Iv

Cpd4

Cors1

Joubert Syndrome And Related Disorders

Jsrd

Familial Aplasia Of The Vermis

Joubert Syndrome Related Disorders

Js

Cerebellar Vermis Agenesis

Cerebelloparenchymal Disorder 4

Agenesis Of Cerebellar Vermis

Cerebello-Oculo-Renal Syndrome

Cors

Joubert-Bolthauser Syndrome

Cpd Iv

Classic Joubert Syndrome

Joubert Syndrome Type A

Pure Joubert Syndrome

Cerebello-Oculo-Renal Syndrome 1

Joubert Syndrome-1

Joubert Syndrome, Type 1

Joubert'S Syndrome

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

Meckel Syndrome, Type 1

Meckel Syndrome

Meckel-Gruber Syndrome

Dysencephalia Splanchnocystica

Meckel Syndrome 1

MKS1

Mks

Gruber Syndrome

Meckel-Gruber Syndrome, Type 1

Mes

Dysencephalia Splachnocystica

Meckel Gruber Syndrome

Meckel Syndrome Type 1

Brachydactyly
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

Leukemia, Acute Myeloid

Acute Myeloid Leukemia

Leukemia, Acute Myelogenous

Acute Myelogenous Leukemia

AML

Leukemia, Acute Myeloid, Susceptibility To

Acute Myeloblastic Leukemia

Leukemia, Acute Myeloid, Reduced Survival In, Somatic

Acute Myeloid Leukaemia

Leukemia, Myelocytic, Acute

Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

Secondary Aml

Acute Myelocytic Leukemia

Leukemia, Myeloid, Acute

Acute Myeloid Leukemia, Somatic

Leukemia, Acute Myeloid, Somatic

Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

Acute Myeloblastic Leukaemia

Acute Myelogenous Leukaemia

Aml - Acute Myeloid Leukemia

Acute Myeloid Leukemia With Cebpa Somatic Mutations

Aml With Cebpa Somatic Mutations

Inherited Acute Myeloid Leukemia

Familial Aml

Inherited Aml

Pure Familial Aml

Pure Familial Acute Myeloid Leukemia

Secondary Acute Myeloid Leukemia

Therapy-Related Aml And Myelodysplastic Syndrome

Acute Myeloid Leukemia, Secondary

Acute Non-Lymphoblastic Leukemia

Acute Non-Lymphocytic Leukemia

Acute Biphenotypic Leukemia

Acute Undifferentiated Leukemia

Acute Myeloblastic Leukaemia With Multilineage Dysplasia

Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

Acute Myeloid Leukaemia With Myelodysplasia-Related Features

Microphthalmia

Microphthalmos

Isolated Anophthalmia-Microphthalmia Syndrome

Isolated Microphthalmia-Anophthalmia-Coloboma

Simple Microphthalmos

Clinical Anophthalmia

Isolated Anophthalmia - Microphthalmia

Isolated Pure Microphthalmia

Mac Spectrum

Microphthalmia-Anophthalmia-Coloboma Spectrum

Primitive Anophthalmia

Globe Of Eye Small

Small Eyeball

Hypoplasia Of Eye

Isolated Nanophthalmos

Rudimentary Eye

Dysplasia Of Eye

Breast Cancer

Breast Carcinoma

Breast Cancer, Familial

Malignant Neoplasm Of Breast

Male Breast Cancer

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

Peripheral T-Cell Lymphoma

Lymphoma T-Cell Peripheral

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

Charcot-Marie-Tooth Disease Axonal Type 2f

CMT2F

Charcot-Marie-Tooth Disease, Neuronal, Type 2f

Charcot-Marie-Tooth Neuropathy, Type 2f

Autosomal Dominant Charcot-Marie-Tooth Disease Type 2f

Charcot-Marie-Tooth Neuropathy Type 2f

Charcot-Marie-Tooth Neuronal Type 2f

Charcot-Marie-Tooth Disease Type 2f

Cmt 2f

Charcot Marie Tooth Disease Type 2f

Charcot-Marie-Tooth Disease 2f

Charcot-Marie-Tooth Disease Neuronal Type 2f

Charcot-Marie-Tooth Disease, Type 2f

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 HDAC6 VGNC VGNC:50613
Rattus norvegicus HDAC6 RGD RGD:619981
Macaca mulatta HDAC6 VGNC VGNC:73164
Mus musculus HDAC6 MGD MGI:1333752
Canis familiaris HDAC6 VGNC VGNC:50630
Felis catus HDAC6 VGNC VGNC:62769
Others HDAC6 NCBI