1. Gene
  2. HSPA8 - heat shock protein family A (Hsp70) member 8 Gene

HSPA8 - heat shock protein family A (Hsp70) member 8 Gene

Homo sapiens

Also known as LAP1; HSC54; HSC70; HSC71; HSP71; HSP73; LAP-1; NIP71; HEL-33; HSPA10; HEL-S-72p

Gene ID: 3312 | Gene type: protein coding

About HSPA8

Cytogenetic location: 11q24.1 Genomic coordinates (GRCh38): 11:123,057,489-123,062,462 (from NCBI)

This gene has 24 transcripts (splice variants), 316 orthologues and 13 paralogues. Ubiquitous expression in brain (RPKM 443.0), kidney (RPKM 352.5) and 25 other tissues.

Summary

This gene encodes a member of the heat shock protein 70 family, which contains both heat-inducible and constitutively expressed members. This protein belongs to the latter group, which are also referred to as heat-shock cognate proteins. It functions as a chaperone, and binds to nascent polypeptides to facilitate correct folding. It also functions as an ATPase in the disassembly of clathrin-coated vesicles during transport of membrane components through the cell. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2011]

HSPA8 Products(2)

mRNA Protein Name
NM_006597.6 NP_006588.1 heat shock cognate 71 kDa protein isoform 1
NM_153201.4 NP_694881.1 heat shock cognate 71 kDa protein isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables ATP binding IDA
IDA: Inferred from direct assay
23921388 GOA
enables ATP-dependent protein disaggregase activity IDA
IDA: Inferred from direct assay
23921388 GOA
enables C3HC4-type RING finger domain binding IPI
IPI: Inferred from physical interaction
25281747 GOA
enables G protein-coupled receptor binding IPI
IPI: Inferred from physical interaction
12150907 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
23921388 GOA
enables heat shock protein binding IPI
IPI: Inferred from physical interaction
17182002 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9305631 GOA
enables protein-folding chaperone binding IPI
IPI: Inferred from physical interaction
16207813 GOA
enables protein-macromolecule adaptor activity IDA
IDA: Inferred from direct assay
2799391 GOA
enables protein-macromolecule adaptor activity IPI
IPI: Inferred from physical interaction
16207813 GOA
enables receptor ligand activity IDA
IDA: Inferred from direct assay
17785435 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
12150907 GOA
enables unfolded protein binding IDA
IDA: Inferred from direct assay
21231916 GOA
Biological Process GO Annotation Evidence Reference Source
involved in ATP metabolic process IDA
IDA: Inferred from direct assay
23921388 GOA
involved in clathrin coat disassembly IDA
IDA: Inferred from direct assay
8524399 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
10722728 GOA
involved in negative regulation of NLRP3 inflammasome complex assembly IDA
IDA: Inferred from direct assay
36586411 GOA
involved in negative regulation of supramolecular fiber organization IDA
IDA: Inferred from direct assay
23921388 GOA
involved in positive regulation of cell migration IDA
IDA: Inferred from direct assay
17785435 GOA
involved in protein refolding IDA
IDA: Inferred from direct assay
21231916 GOA
involved in protein targeting to lysosome involved in chaperone-mediated autophagy IDA
IDA: Inferred from direct assay
11559757 GOA
involved in protein targeting to lysosome involved in chaperone-mediated autophagy IMP
IMP: Inferred from mutant phenotype
26212789 GOA
involved in regulation of protein stability IMP
IMP: Inferred from mutant phenotype
26212789 GOA
Cellular Component GO Annotation Evidence Reference Source
part of Prp19 complex IDA
IDA: Inferred from direct assay
20176811 GOA
part of Prp19 complex IPI
IPI: Inferred from physical interaction
20176811 GOA
located in cytosol IDA
IDA: Inferred from direct assay
21231916 GOA
located in extracellular exosome IDA
IDA: Inferred from direct assay
19028452 GOA
is active in extracellular space IDA
IDA: Inferred from direct assay
16502470 GOA
is active in lysosomal membrane IDA
IDA: Inferred from direct assay
11559757 GOA
located in nucleus IDA
IDA: Inferred from direct assay
20176811 GOA
part of protein folding chaperone complex IPI
IPI: Inferred from physical interaction
16207813 GOA
part of ribonucleoprotein complex IDA
IDA: Inferred from direct assay
17289661 GOA
part of spliceosomal complex IPI
IPI: Inferred from physical interaction
20176811 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

HSPA8 Protein Structure

HSP70

HSP70: Hsp70 protein (6 - 612)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 600
  • 646 a.a.
Protein Preferred Names Protein Names

heat shock cognate 71 kDa protein

LPS-associated protein 1

HSPA8 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
HSPA8 P11142 BAG1 Homo sapiens Q99933 19800331
Intra
HSPA8 P11142 P01308-PRO_0000015820 Homo sapiens P01308-PRO_0000015820
NMR
29764935
Intra
HSPA8 P11142 TRIM38 Homo sapiens O00635 32296183
Intra
HSPA8 P11142 TRIM38 Homo sapiens O00635 25416956
Intra
HSPA8 P11142 TRIM38 Homo sapiens O00635 25416956
Intra
HSPA8 P11142 TRIM38 Homo sapiens O00635 32296183
Intra
HSPA8 P11142 SF3A2 Homo sapiens Q15428 33961781
Intra
HSPA8 P11142 SF3A2 Homo sapiens Q15428 28514442
Intra
HSPA8 P11142 BAG4 Homo sapiens O95429 32296183
Intra
HSPA8 P11142 BAG4 Homo sapiens O95429 32296183
Intra
HSPA8 P11142 BAG4 Homo sapiens O95429 29568061
Intra
HSPA8 P11142 EGFR Homo sapiens P00533 24658140
Intra
HSPA8 P11142 EGFR Homo sapiens P00533 24658140
Intra
HSPA8 P11142 HLA-H Homo sapiens P01893
FPS
29764935
Intra
HSPA8 P11142 HLA-H Homo sapiens P01893
NMR
29764935
Intra
HSPA8 P11142 BAG2 Homo sapiens O95816 29568061
Intra
HSPA8 P11142 BAG2 Homo sapiens O95816 33961781
Intra
HSPA8 P11142 BAG2 Homo sapiens O95816
Y2H
22365833
Intra
HSPA8 P11142 BAG2 Homo sapiens O95816 29568061
Intra
HSPA8 P11142 HSPBP1 Homo sapiens Q9NZL4 25416956
Intra
HSPA8 P11142 HSPBP1 Homo sapiens Q9NZL4 35271311
Intra
HSPA8 P11142 HSPBP1 Homo sapiens Q9NZL4 29568061
Intra
HSPA8 P11142 HSPBP1 Homo sapiens Q9NZL4 25416956
Intra
HSPA8 P11142 HSPBP1 Homo sapiens Q9NZL4 29568061
Intra
HSPA8 P11142 HSPBP1 Homo sapiens Q9NZL4 33961781
Intra
HSPA8 P11142 HSPBP1 Homo sapiens Q9NZL4 28514442
Intra
HSPA8 P11142 HSPBP1 Homo sapiens Q9NZL4 25416956
Intra
HSPA8 P11142 HSPA4 Homo sapiens P34932 29568061
Intra
HSPA8 P11142 HSPA4 Homo sapiens P34932 30021884
Intra
HSPA8 P11142 HSPA4 Homo sapiens P34932 33961781
Intra
HSPA8 P11142 HSPA4 Homo sapiens P34932 29568061
Intra
HSPA8 P11142 STUB1 Homo sapiens Q9UNE7 16275660
Intra
HSPA8 P11142 STUB1 Homo sapiens Q9UNE7 16275660
Intra
HSPA8 P11142 STUB1 Homo sapiens Q9UNE7 29568061
Intra
HSPA8 P11142 STUB1 Homo sapiens Q9UNE7 29568061
Intra
HSPA8 P11142 STUB1 Homo sapiens Q9UNE7
ITC
20618441
Intra
HSPA8 P11142 MAPT Homo sapiens P10636 33961781
Intra
HSPA8 P11142 MAPT Homo sapiens P10636
FPS
29764935
Intra
HSPA8 P11142 MAPT Homo sapiens P10636
NMR
29764935
Intra
HSPA8 P11142 LDHA Homo sapiens P00338 23523103
Intra
HSPA8 P11142 AICDA Homo sapiens Q9GZX7 22085931
Intra
HSPA8 P11142 ESRP2 Homo sapiens Q9H6T0 33961781
Intra
HSPA8 P11142 NCF1 Homo sapiens P14598 25910212
Intra
HSPA8 P11142 HTT Homo sapiens P42858 32814053
Intra
HSPA8 P11142 HTT Homo sapiens P42858 32814053
Intra
HSPA8 P11142 HTT Homo sapiens P42858 32814053
Intra
HSPA8 P11142 LRRK2 Homo sapiens Q5S007 23455607
Intra
HSPA8 P11142 ATP13A2 Homo sapiens Q9NQ11 22645275
Intra
HSPA8 P11142 EIF2AK1 Homo sapiens Q9BQI3 31273097
Intra
HSPA8 P11142 EIF2AK1 Homo sapiens Q9BQI3 29568061
Intra
HSPA8 P11142 ARRB2 Homo sapiens P32121 17620599
Intra
HSPA8 P11142 GAK Homo sapiens O14976 33961781
Intra
HSPA8 P11142 GAK Homo sapiens O14976 24510904
Intra
HSPA8 P11142 GAK Homo sapiens O14976 28514442
Intra
HSPA8 P11142 GAK Homo sapiens O14976 29568061
Intra
HSPA8 P11142 ARRB1 Homo sapiens P49407 17620599
Intra
HSPA8 P11142 MAPT Homo sapiens P10636-6
FPS
29764935
Intra
HSPA8 P11142 MAPT Homo sapiens P10636-6
NMR
29764935
Intra
HSPA8 P11142 JUN Homo sapiens P05412 20195357
Intra
HSPA8 P11142 ATXN1 Homo sapiens P54253 32814053
Intra
HSPA8 P11142 ATXN1 Homo sapiens P54253 32814053
Intra
HSPA8 P11142 ATXN1 Homo sapiens P54253 32814053
Intra
HSPA8 P11142 STXBP1 Homo sapiens P61764 25910212
Cross
HSPA8 P11142 EBNA-LP Epstein-Barr virus Q8AZK7 18457437
Cross
HSPA8 P11142 M Influenza A virus P03485 17022977
Cross
HSPA8 P11142 M Influenza A virus P03485 17022977
Cross
HSPA8 P11142 Q99IB8-PRO_0000045603 Hepatitis C virus Q99IB8-PRO_0000045603 24136289
Cross
HSPA8 P11142 Q99IB8-PRO_0000045603 Hepatitis C virus Q99IB8-PRO_0000045603 24136289
Cross
HSPA8 P11142 Q99IB8-PRO_0000045603 Hepatitis C virus Q99IB8-PRO_0000045603
Y2H
24136289
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant HSPA8 Proteins

Cat. No. Product Name Accession Purity
HY-P73915 HSPA8/HSC70 Protein, Human (His, Solution) P11142-1 (M1-D646) ≥95%

HSPA8 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80708 Hsc70 Antibody WB, IHC-P, IP Human, Mouse, Rat, Hamster

Related Diseases

Diseases Alias
Auditory System Disease

Ear Diseases

Ear And Mastoid Disease

Borna Disease

Enzootic Encephalomyelitis

Ischemia

Acute Coronary Syndrome

Arthritis

Inflammatory Joint Disease

Inflammatory Disorder Of Joint

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

Sensorineural Hearing Loss

Sensory Hearing Loss

Sensorineural Deafness

Sensorineural Hearing Loss Disorder

Hearing Loss, Sensorineural

Central Hearing Loss

High Frequency Deafness

High Frequency Hearing Loss

High-Frequency Hearing Loss

Perceptive Deafness

Perceptive Hearing Loss

Perceptive Hearing Loss Or Deafness

Hearing Loss Sensorineural

Deafness Sensorineural

Hearing Loss High-Frequency

Hearing Loss, Central

Hearing Loss, High-Frequency

Axonal Neuropathy
Colorectal Cancer

Colon Cancer

Colorectal Carcinoma

Colon Carcinoma

Colorectal Cancer, Susceptibility To

Carcinoma Of Colon

CRC

Colorectal Cancer With Chromosomal Instability, Somatic

Colon Cancer, Somatic

Colon Cancer, Susceptibility To

Colonic Neoplasms

Colorectal Neoplasms

Colorectal Cancer, Somatic

Colon Cancer, Advanced, Somatic

Colonic Carcinoma

Colorectal Carcinomas

Colon Cancers

Colorectal Cancers

Cancer, Colorectal, Somatic

Cancer, Colon

Cancer, Colorectal, Susceptibility To

Colorectal Neoplasm

Colonic Neoplasm

Malignant Tumor Of Colon

Cystic Fibrosis

Mucoviscidosis

CF

Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

Cystic Fibrosis Lung Disease, Modifier Of

Cystic Fibrosis Of Pancreas

Fibrocystic Disease Of Pancreas

Cf - [Cystic Fibrosis]

Cystic Fibrosis Nos

Fibrocystic Disease

Fibrocystic Disease Of The Pancreas

Mucoviscidosis Of Pancreas

Nonproliferative Fibrocystic Disease

Pancreatic Cystic Fibrosis

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

Meniere Disease

Meniere'S Disease

Otogenic Vertigo

Ménière Disease

Ménière'S Disease

Mnire'S Vertigo

Auditory Vertigo

Aural Vertigo

Meniere'S Syndrome

Ménière'S Vertigo

Primary Endolymphatic Hydrops

Menieres Disease

Vertigo, Aural

Labyrinth Hydrops

Labyrinthine Hydrops

Labyrinthine Vertigo

Ménière Syndrome

Ménière Vertigo

Idiopathic Endolymphatic Hydrops

Muscular Atrophy

Muscle Wasting

Amyotrophia

Wasting - Muscle

Skeletal Muscle Atrophy

Lung Cancer

Lung Carcinoma

Non-Small Cell Lung Carcinoma

Lung Cancer, Susceptibility To

Lung Cancer, Protection Against

Adenocarcinoma Of Lung, Somatic

Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer

Lung Neoplasm

Carcinoma Of Lung

Lung Non-Small Cell Carcinoma

Non-Small Cell Lung Cancer

Nsclc

Lung Neoplasms

Malignant Neoplasm Of Lung

Alveolar Cell Carcinoma

Nonsmall Cell Lung Cancer, Somatic

Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In

Nonsmall Cell Lung Cancer, Susceptibility To

Lung Cancer, Somatic

Lung Cancer, Resistance To

Cancer Of Lung

Cancer Of Bronchus

Cancer Of The Lung

Lung Malignancies

Lung Malignant Tumors

Malignant Lung Tumor

Malignant Tumor Of Lung

Pulmonary Cancer

Pulmonary Carcinoma

Pulmonary Neoplasms

Respiratory Carcinoma

LNCR

Adenocarcinoma Of Lung

Neoplasm Of Lung

Cancer Lung

Carcinoma Non-Small Cell Lung

Carcinoma, Non-Small-Cell Lung

Lung Cancers

Lung Carcinomas

Cancer, Lung

Cancer, Lung, Non-Small Cell

Primary Malignant Neoplasm Of Lung

Bronchioloalveolar Adenocarcinoma

Complement Component 7 Deficiency

C7 Deficiency

C7D

Myocardial Infarction

Heart Attack

Myocardial Infarction, Susceptibility To

Myocardial Infarction 1

Myocardial Infarction, Protection Against

Myocardial Infarction, Decreased Susceptibility To

Myocardial Infarction, Decreased

Myocardial Infarct

MCI1

Premature Myocardial Infarction

Myocardial Infarction, Susceptibility To, Type 1

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

Gastric Cancer

Stomach Cancer

Gastric Carcinoma

Stomach Carcinoma

Gastric Cancer, Somatic

Gastric Neoplasm

Carcinoma Of Stomach

Stomach Neoplasms

Malignant Neoplasm Of Stomach

Gastric Cancer Risk After H. Pylori Infection

Cancer Of The Stomach

Adult Stomach Cancer

Adult Stomach Carcinoma

GASC

Gastric Cancer Intestinal

Gastric Cancers

Gastric Carcinomas

Cancer, Gastric

Stomach Neoplasm

Malignant Neoplasm Of Body Of Stomach

Malignant Tumor Of Lesser Curve Of Stomach

Gastrocarcinoma Of Unspecified Site

Leather Bottle Stomach

Carcinoma Of Fundus Of Stomach

Cancer Of Fundus Of Stomach

Primary Malignant Neoplasm Of Body Of Stomach

Cancer Of Body Of Stomach

Primary Malignant Neoplasm Of Pyloric Antrum

Pyloric Antrum Cancer

Malignant Tumour Of Stomach

Dystonia

Dystonic Disease

Dystonic Disorder

Dystonia Disorders

Neuroleptic Dyskinesia

Breast Cancer

Breast Carcinoma

Male Breast Cancer

Breast Cancer, Familial

Malignant Neoplasm Of Breast

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

Stroke, Ischemic

Cerebral Infarction

Stroke

Ischemic Stroke

Cerebrovascular Accident

Cerebral Infarction, Susceptibility To

Stroke, Ischemic, Susceptibility To

Cerebral Infarct

Ischemic Stroke, Susceptibility To

Stroke, Susceptibility To

Cva - Cerebral Infarction

ISCHSTR

Ischemic Cerebrovascular Accident

Schizophrenia

SCZD

Schizophrenia With Or Without An Affective Disorder

Schizophrenia 12

Schizophrenia, Susceptibility To

Schizophrenia-1

Dementia Praecox

Schizophrenia 1

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

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

Leukemia, Chronic Myeloid

Chronic Myeloid Leukemia

Chronic Myelogenous Leukemia

CML

Chronic Granulocytic Leukemia

Leukemia, Philadelphia Chromosome-Positive, Resistant To Imatinib

Chronic Myeloid Leukaemia

Chronic Granulocytic Leukaemia

Chronic Myelogenous Leukaemia

Myeloid Leukemia, Chronic

Leukemia, Chronic Myelogenous

Leukemia, Chronic Myeloid, Philadelphia Chromosome Positive, Somatic

Cml - Chronic Myelogenous Leukemia

Cgl

Chronic Myelocytic Leukemia

Leukemia, Chronic Myeloid, Atypical

ACML

Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative

Myeloid Leukemia Chronic

Leukemia, Myeloid, Chronic

Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative

Cml- [Chronic Myeloid Leukaemia]

Cgl - [Chronic Granulocytic Leukaemia]

Chronic Myelocytic Leukaemia

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

Lipoprotein Quantitative Trait Locus

Coronary Artery Disease

Coronary Artery Anomaly

Coronary Artery Disease, Susceptibility To

Myocardial Ischemia

Congenital Anomaly Of Coronary Artery

Coronary Arteriosclerosis

Coronary Disease

Coronary Heart Disease

Coronary Artery Disorder

LPAQTL

Lpa Deficiency, Congenital

Coronary Artery Abnormality

Coronary Artery Anomaly, Congenital

Chd

Coronary Syndrome

Congenital Malformations Of Coronary Vessels

Malformation Of Coronary Vessels

Congenital Coronary Artery Anomaly

Congenital Coronary Artery Deformity

Congenital Coronary Artery Disorder

Abnormal Coronary Artery

Congenital Coronary Artery Malposition

Congenital Coronary Disease

Congenital Anomaly Of Coronary Arteries

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

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

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

Type 2 Diabetes Mellitus

Insulin Resistance

NIDDM

Type 2 Diabetes

Diabetes Mellitus, Non-Insulin-Dependent

T2D

Noninsulin-Dependent Diabetes Mellitus

Diabetes Mellitus, Type Ii

Maturity-Onset Diabetes

Insulin Resistance, Severe, Digenic

Diabetes Mellitus, Type 2

Diabetes Mellitus, Noninsulin-Dependent

Diabetes Mellitus, Noninsulin-Dependent, Association With

Diabetes Mellitus, Noninsulin-Dependent, Late Onset

Hypertension, Insulin Resistance-Related, Susceptibility To

Insulin Resistance, Susceptibility To

Non-Insulin-Dependent Diabetes Mellitus

Type Ii Diabetes Mellitus

Adult-Onset Diabetes Mellitus

Maturity-Onset Diabetes Mellitus

Diabetes Mellitus Type 2

Type Ii Diabetes

Type 2 Diabetes Mellitus, Susceptibility To

Diabetes, Type 2

Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

Diabetes Mellitus, Type 2, Susceptibility To

Diabetes Mellitus, Noninsulin-Dependent, 2

Diabetes Mellitus, Type Ii, Susceptibility To

Hypertension, Insulin Resistance-Related

Adult-Onset Diabetes

Aodm

Diabetes Mellitus, Adult-Onset

Diabetes Mellitus Type Ii

Diabetes Mellitus Type 2, Susceptibility To

Diabetes, Type Ii, Susceptibility To

Diabetes Type 2

Diabetes Mellitus

Adult Onset Diabetes

Maturity Onset Diabetes

Nonketotic Diabetes

Non-Insulin Dependent Diabetes Mellitus

T2dm - [Type 2 Diabetes Mellitus]

Niddm - [Non Insulin Dependent Diabetes Mellitus]

Dm2

Dm Type Ii

Diabetic Type 2

Insulin Requiring Type 2 Diabetes

Noninsulin Dependent Diabetes

Non-Insulin-Dependent Diabetes Mellitus Without Complications

Diabetes Due To Insulin Secretory Defect

Diabetes Mellitus Due To Insulin Secretory Defect

Non-Insulin-Dependent Diabetes Of The Young

Senile Diabetes

Nonketotic Hyperglycaemia

Stable Diabetes

Nervous System Disease

Abnormality Of The Nervous System

Nervous System Diseases

Nervous System Disorder

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
Felis catus HSPA8 VGNC VGNC:82045
Canis familiaris HSPA8 VGNC VGNC:59028
Rattus norvegicus HSPA8 RGD RGD:621725
Bos taurus HSPA8 VGNC VGNC:54632
Macaca mulatta HSPA8 VGNC VGNC:101093
Mus musculus HSPA8 MGD MGI:105384
Others HSPA8 NCBI