1. Gene
  2. HSPB7 - heat shock protein family B (small) member 7 Gene

HSPB7 - heat shock protein family B (small) member 7 Gene

Homo sapiens

Also known as cvHSP

Gene ID: 27129 | Gene type: protein coding

About HSPB7

Cytogenetic location: 1p36.13 Genomic coordinates (GRCh38): 1:16,014,029-16,019,594 (from NCBI)

This gene has 7 transcripts (splice variants), 256 orthologues and 8 paralogues. Biased expression in heart (RPKM 547.7) and fat (RPKM 156.2).

Summary

This gene encodes a small heat shock family B member that can heterodimerize with similar heat shock proteins. Defects in this gene are associated with advanced heart failure. In addition, the encoded protein may be a tumor suppressor in the p53 pathway, with defects in this gene being associated with renal cell carcinoma. [provided by RefSeq, Mar 2017]

HSPB7 Products(8)

mRNA Protein Name
NM_001349682.2 NP_001336611.1 heat shock protein beta-7 isoform 1
NM_001349683.2 NP_001336612.1 heat shock protein beta-7 isoform 3
NM_001349685.2 NP_001336614.1 heat shock protein beta-7 isoform 4
NM_001349686.2 NP_001336615.1 heat shock protein beta-7 isoform 5
NM_001349687.2 NP_001336616.1 heat shock protein beta-7 isoform 6
NM_001349688.2 NP_001336617.1 heat shock protein beta-7 isoform 7
NM_001349689.2 NP_001336618.1 heat shock protein beta-7 isoform 8
NM_014424.5 NP_055239.1 heat shock protein beta-7 isoform 2
Gene Ontology
  • Molecular Function
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
14594798 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cytoplasm IDA
IDA: Inferred from direct assay
19464326 GOA
located in nucleus IDA
IDA: Inferred from direct assay
19464326 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

HSPB7 Protein Structure

HSP20

HSP20: Hsp20/alpha crystallin family (76 - 159)

  • 0
  • 100
  • 170 a.a.
Protein Preferred Names Protein Names

heat shock protein beta-7

cardiovascular heat shock protein

HSPB7 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
HSPB7 Q9UBY9 REL Homo sapiens Q04864-2 32296183
Intra
HSPB7 Q9UBY9 REL Homo sapiens Q04864-2 32296183
Intra
HSPB7 Q9UBY9 TEPSIN Homo sapiens Q96N21 32296183
Intra
HSPB7 Q9UBY9 TEPSIN Homo sapiens Q96N21 32296183
Intra
HSPB7 Q9UBY9 UBXN1 Homo sapiens Q04323-2 32296183
Intra
HSPB7 Q9UBY9 UBXN1 Homo sapiens Q04323-2 32296183
Intra
HSPB7 Q9UBY9 PIP4K2B Homo sapiens P78356-2 32296183
Intra
HSPB7 Q9UBY9 PIP4K2B Homo sapiens P78356-2 32296183
Intra
HSPB7 Q9UBY9 DYNLT1 Homo sapiens P63172 32296183
Intra
HSPB7 Q9UBY9 DYNLT1 Homo sapiens P63172 32296183
Intra
HSPB7 Q9UBY9 C22orf15 Homo sapiens Q8WYQ4-2 32296183
Intra
HSPB7 Q9UBY9 C22orf15 Homo sapiens Q8WYQ4-2 32296183
Intra
HSPB7 Q9UBY9 TCF4 Homo sapiens P15884-3 32296183
Intra
HSPB7 Q9UBY9 TCF4 Homo sapiens P15884-3 32296183
Intra
HSPB7 Q9UBY9 REL Homo sapiens Q04864 25416956
Intra
HSPB7 Q9UBY9 REL Homo sapiens Q04864 25416956
Intra
HSPB7 Q9UBY9 SF3B4 Homo sapiens Q15427 25416956
Intra
HSPB7 Q9UBY9 PDLIM7 Homo sapiens Q9NR12 32296183
Intra
HSPB7 Q9UBY9 PDLIM7 Homo sapiens Q9NR12 32296183
Intra
HSPB7 Q9UBY9 PRDM14 Homo sapiens Q9GZV8 25416956
Intra
HSPB7 Q9UBY9 SYCE1 Homo sapiens Q8N0S2 25416956
Intra
HSPB7 Q9UBY9 HSPB8 Homo sapiens Q9UJY1 14594798
Intra
HSPB7 Q9UBY9 HSPB8 Homo sapiens Q9UJY1 32296183
Intra
HSPB7 Q9UBY9 HSPB8 Homo sapiens Q9UJY1 32296183
Intra
HSPB7 Q9UBY9 HSPB8 Homo sapiens Q9UJY1
Y2H
14594798
Intra
HSPB7 Q9UBY9 HSPB8 Homo sapiens Q9UJY1 14594798
Intra
HSPB7 Q9UBY9 HSPB8 Homo sapiens Q9UJY1 25416956
Intra
HSPB7 Q9UBY9 HSPB8 Homo sapiens Q9UJY1 32296183
Intra
HSPB7 Q9UBY9 TRIM23 Homo sapiens P36406 25416956
Intra
HSPB7 Q9UBY9 TRIM23 Homo sapiens P36406 25416956
Intra
HSPB7 Q9UBY9 DDIT4L Homo sapiens Q96D03 32296183
Intra
HSPB7 Q9UBY9 DDIT4L Homo sapiens Q96D03 32296183
Intra
HSPB7 Q9UBY9 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
HSPB7 Q9UBY9 PLEKHF2 Homo sapiens Q9H8W4 25416956
Intra
HSPB7 Q9UBY9 PLEKHF2 Homo sapiens Q9H8W4 25416956
Intra
HSPB7 Q9UBY9 PLEKHF2 Homo sapiens Q9H8W4 32296183
Intra
HSPB7 Q9UBY9 PLEKHF2 Homo sapiens Q9H8W4 25416956
Intra
HSPB7 Q9UBY9 CEP76 Homo sapiens Q8TAP6 25416956
Intra
HSPB7 Q9UBY9 CEP76 Homo sapiens Q8TAP6 25416956
Intra
HSPB7 Q9UBY9 CEP76 Homo sapiens Q8TAP6 32296183
Intra
HSPB7 Q9UBY9 CEP76 Homo sapiens Q8TAP6 25416956
Intra
HSPB7 Q9UBY9 CEP76 Homo sapiens Q8TAP6 32296183
Intra
HSPB7 Q9UBY9 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
HSPB7 Q9UBY9 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
HSPB7 Q9UBY9 IKZF3 Homo sapiens Q9UKT9 32296183
Intra
HSPB7 Q9UBY9 FLNA Homo sapiens P21333-2 28514442
Intra
HSPB7 Q9UBY9 FLNA Homo sapiens P21333-2 32296183
Intra
HSPB7 Q9UBY9 FLNA Homo sapiens P21333-2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant HSPB7 Proteins

Cat. No. Product Name Accession Purity
HY-P70929 PSG2 Protein, Human (His) Q9UBY9 (M1-I170) ≥95%

Related Diseases

Diseases Alias
Paraneoplastic Polyneuropathy
Distal Hereditary Motor Neuronopathy Type 2

Distal Hereditary Motor Neuropathy, Type Ii

Distal Hereditary Motor Neuropathy Type 2

Distal Hereditary Motor Neuropathy Type Ii

Hmn Ii

Hmn2

Distal Hereditary Motor Neuronopathy, Type Ii

Distal Spinal Muscular Atrophy Type 2

Dhmn2

Dsma2

Neuropathy, Motor, Distal, Hereditary, Type Ii

Spinal Muscular Atrophy, Jerash Type

Myopathy, Myofibrillar, 5

Myofibrillar Myopathy 5

MFM5

Myopathy, Myofibrillar, Filamin C-Related

Filaminopathy, Autosomal Dominant

Filaminopathy

Muscle Filaminopathy

Autosomal Dominant Filaminopathy

Mfm Filamin C-Related

Myopathy Myofibrillar Filamin C-Related

Myopathy, Myofibrillar, Type 5

Systolic Heart Failure

Heart Failure, Systolic

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]

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

Hypertrophic Cardiomyopathy

Hypertrophic Obstructive Cardiomyopathy

Cardiomyopathy, Hypertrophic

Cardiomyopathy Hypertrophic Obstructive

Cardiomyopathy, Hypertrophic, Familial

Idiopathic Myocardial Hypertrophy

Idiopathic Hypertrophic Cardiomyopathy

Obstructive Idiopathic Hypertrophic Cardiomyopathy

Obstructive Cardiomyopathy

Idiopathic Hypertrophic Subaortic Stenosis

Muscular Subaortic Stenosis

Hypertrophic Obstructive Subaortic Stenosis

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
Mus musculus HSPB7 MGD MGI:1352494
Rattus norvegicus HSPB7 RGD RGD:62021
Macaca mulatta HSPB7 VGNC VGNC:99972
Canis familiaris HSPB7 VGNC VGNC:52138
Felis catus HSPB7 VGNC VGNC:80236
Bos taurus HSPB7 VGNC VGNC:49068