HDAC6 - histone deacetylase 6 Gene

Also Known as HD6; JM21; CPBHM; PPP1R90

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10013

About 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.

Summary

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 Products (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
Molecular Function GO Annotation Evidence References Source
enables Hsp90 protein binding IDA
IDA: Inferred from direct assay
15916966 GOA
enables RNA polymerase II cis-regulatory region sequence-specific DNA binding IDA
IDA: Inferred from direct assay
24413532 GOA
NOT enables acetylspermidine deacetylase activity IDA
IDA: Inferred from direct assay
28516954 GOA
enables alpha-tubulin binding IDA
IDA: Inferred from direct assay
19228685 GOA
enables beta-catenin binding IPI
IPI: Inferred from physical interaction
18356165 GOA
enables dynein complex binding IDA
IDA: Inferred from direct assay
14675537 GOA
enables histone deacetylase activity IDA
IDA: Inferred from direct assay
10220385 GOA
enables histone deacetylase activity IMP
IMP: Inferred from mutant phenotype
23322205 GOA
enables histone deacetylase binding IPI
IPI: Inferred from physical interaction
12620231 GOA
enables microtubule binding IDA
IDA: Inferred from direct assay
19228685 GOA
enables misfolded protein binding EXP
EXP: Inferred from Experiment
17785525 GOA
enables polyubiquitin modification-dependent protein binding IDA
IDA: Inferred from direct assay
14675537 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16919237 GOA
enables protein lysine deacetylase activity IDA
IDA: Inferred from direct assay
28516954 GOA
enables tau protein binding IDA
IDA: Inferred from direct assay
18636984 GOA
enables transcription corepressor binding IPI
IPI: Inferred from physical interaction
12535528 GOA
enables tubulin deacetylase activity EXP
EXP: Inferred from Experiment
12024216 GOA
enables tubulin deacetylase activity IDA
IDA: Inferred from direct assay
12620231 GOA
enables tubulin deacetylase activity IMP
IMP: Inferred from mutant phenotype
19457097 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
21753002 GOA
Biological Process GO Annotation Evidence References Source
involved in aggresome assembly IMP
IMP: Inferred from mutant phenotype
14675537 GOA
involved in axonal transport of mitochondrion IGI
IGI: Inferred from genetic interaction
28105056 GOA
involved in cellular response to hydrogen peroxide IMP
IMP: Inferred from mutant phenotype
18606987 GOA
involved in cellular response to topologically incorrect protein IMP
IMP: Inferred from mutant phenotype
16192271 GOA
involved in cilium disassembly IDA
IDA: Inferred from direct assay
26246421 GOA
involved in cilium disassembly IMP
IMP: Inferred from mutant phenotype
17604723 GOA
involved in intracellular protein transport IMP
IMP: Inferred from mutant phenotype
16192271 GOA
involved in lysosome localization IMP
IMP: Inferred from mutant phenotype
16192271 GOA
involved in negative regulation of aggrephagy IDA
IDA: Inferred from direct assay
31857589 GOA
involved in negative regulation of gene expression, epigenetic IMP
IMP: Inferred from mutant phenotype
24413532 GOA
involved in negative regulation of protein-containing complex assembly IMP
IMP: Inferred from mutant phenotype
23962722 GOA
involved in negative regulation of protein-containing complex disassembly IMP
IMP: Inferred from mutant phenotype
15916966 GOA
involved in negative regulation of proteolysis IMP
IMP: Inferred from mutant phenotype
18356165 GOA
involved in peptidyl-lysine deacetylation IMP
IMP: Inferred from mutant phenotype
18356165 GOA
NOT involved in polyamine deacetylation IDA
IDA: Inferred from direct assay
28516954 GOA
involved in polyubiquitinated misfolded protein transport IMP
IMP: Inferred from mutant phenotype
14675537 GOA
involved in positive regulation of epithelial cell migration IMP
IMP: Inferred from mutant phenotype
12024216 GOA
involved in positive regulation of peptidyl-serine phosphorylation IMP
IMP: Inferred from mutant phenotype
23962722 GOA
acts upstream of positive regulation of signaling receptor activity IMP
IMP: Inferred from mutant phenotype
15916966 GOA
involved in protein deacetylation IDA
IDA: Inferred from direct assay
28516954 GOA
involved in protein deacetylation IMP
IMP: Inferred from mutant phenotype
15916966 GOA
involved in protein quality control for misfolded or incompletely synthesized proteins IMP
IMP: Inferred from mutant phenotype
14675537 GOA
involved in regulation of macroautophagy IMP
IMP: Inferred from mutant phenotype
16192271 GOA
involved in regulation of protein stability IMP
IMP: Inferred from mutant phenotype
23580651 GOA
involved in response to growth factor IMP
IMP: Inferred from mutant phenotype
18356165 GOA
involved in response to misfolded protein IMP
IMP: Inferred from mutant phenotype
14675537 GOA
NOT involved in spermidine deacetylation IDA
IDA: Inferred from direct assay
28516954 GOA
involved in tubulin deacetylation IDA
IDA: Inferred from direct assay
19228685 GOA
involved in type 2 mitophagy IGI
IGI: Inferred from genetic interaction
20457763 GOA
Cellular Component GO Annotation Evidence References Source
located in aggresome IDA
IDA: Inferred from direct assay
14675537 GOA
located in caveola IDA
IDA: Inferred from direct assay
18356165 GOA
located in cell leading edge IDA
IDA: Inferred from direct assay
12024216 GOA
located in centrosome IDA
IDA: Inferred from direct assay
26246421 GOA
located in ciliary basal body IDA
IDA: Inferred from direct assay
17604723 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
24687993 GOA
part of histone deacetylase complex IDA
IDA: Inferred from direct assay
11948178 GOA
located in inclusion body IDA
IDA: Inferred from direct assay
16192271 GOA
located in microtubule IDA
IDA: Inferred from direct assay
12620231 GOA
part of microtubule associated complex IDA
IDA: Inferred from direct assay
19228685 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
12024216 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

HDAC6 Protein Structure

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.
Protein Preferred Names Protein Names

histone deacetylase 6

  • protein phosphatase 1, regulatory subunit 90

  • tubulin-lysine deacetylase HDAC6

HDAC6 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
HDAC6 Q9UBN7 PRKCA Homo sapiens P17252 21952047
Intra
HDAC6 Q9UBN7 CYLD Homo sapiens Q9NQC7 19893491
Intra
HDAC6 Q9UBN7 CYLD Homo sapiens Q9NQC7 19893491
Intra
HDAC6 Q9UBN7 DCTN1 Homo sapiens Q14203-5 32814053
Intra
HDAC6 Q9UBN7 DCTN1 Homo sapiens Q14203-5 32814053
Intra
HDAC6 Q9UBN7 DCTN1 Homo sapiens Q14203-5 32814053
Intra
HDAC6 Q9UBN7 EGFR Homo sapiens P00533 24658140
Intra
HDAC6 Q9UBN7 EGFR Homo sapiens P00533 20029029
Intra
HDAC6 Q9UBN7 EGFR Homo sapiens P00533 20029029
Intra
HDAC6 Q9UBN7 EGFR Homo sapiens P00533 24658140
Intra
HDAC6 Q9UBN7 PROM1 Homo sapiens O43490 23084749
Intra
HDAC6 Q9UBN7 PROM1 Homo sapiens O43490 23084749
Cross
HDAC6 Q9UBN7 Cttn Mus musculus Q60598
IF
21847094
Intra
HDAC6 Q9UBN7 MYD88 Homo sapiens Q99836 29281743
Intra
HDAC6 Q9UBN7 CTNNB1 Homo sapiens P35222 18356165
Intra
HDAC6 Q9UBN7 CTNNB1 Homo sapiens P35222 23084749
Intra
HDAC6 Q9UBN7 ATP13A2 Homo sapiens Q9NQ11 22645275
Intra
HDAC6 Q9UBN7 PRKN Homo sapiens O60260 19036992
Cross
HDAC6 Q9UBN7 GRK2 Bos taurus P21146 22193721
Cross
HDAC6 Q9UBN7 GRK2 Bos taurus P21146 22193721
Cross
HDAC6 Q9UBN7 Cdc20 Rattus norvegicus Q62623 19167333
Cross
HDAC6 Q9UBN7 Cdc20 Rattus norvegicus Q62623 19167333
Cross
HDAC6 Q9UBN7 Tax Human T-cell leukemia virus 1 P03409 21532619
Cross
HDAC6 Q9UBN7 Tax Human T-cell leukemia virus 1 P03409 21532619
Cross
HDAC6 Q9UBN7 tat Human immunodeficiency virus P04610 21220424
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant HDAC6 Proteins

Cat. No. Product Name Accession Purity
HY-P72224 HDAC6 Protein, Human (His) Q9UBN7-1 (M489-E840) ≥ 90%, as determined by reducing SDS-PAGE.

HDAC6 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80154 HDAC6 Antibody (YA390) WB, ICC/IF, IHC-P, IP Human
HY-P80701 HDAC6 Antibody (YA740) WB Human, Rat
HY-P80701A HDAC6 Antibody (YA740)(PBS only) WB Human, Rat
HY-P86103 HDAC6 Antibody (YA5795) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
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

Diseases Alias
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

Orthologs Information

Species Symbol Source 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