HSPD1

GENERAL INFORMATION

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Gene name

HSPD1

Gene description

Heat shock 60kDa protein 1 (chaperonin)

Protein class

Cancer-related genes
Disease related genes
Mitochondrial proteins
Plasma proteins
Predicted intracellular proteins

Predicted localization

Intracellular

Number of transcripts

8
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HUMAN PROTEIN ATLAS INFORMATION

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RNA tissue category

HPA:Expressed in all
GTEx:Expressed in all

Protein evidence

Evidence at protein level

Protein localization

Granular cytoplasmic expression in most cell types.

ANTIBODY RELIABILITY

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Data reliability
description

Antibody staining mainly consistent with RNA expression data.

Data reliability

Supportive based on 3 antibodies.
HPA001523 , CAB002775 , CAB072816
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RNA AND PROTEIN EXPRESSION SUMMARY

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RNA expression (FPKM) Protein expression (score)
Brain
Endocrine tissues
Bone marrow & immune system
Muscle tissues
Lung
Nasopharynx
N/A
N/A
Bronchus
N/A
Liver & gallbladder
Pancreas
Gastrointestinal tract
Kidney & urinary bladder
Male tissues
Female tissues
Adipose & soft tissue
Skin
Cerebral cortex

Lymph node

Liver

Pancreas

Colon

Kidney

Testis



PROTEIN EXPRESSION OVERVIEW

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Organ

Expression



RNA EXPRESSION OVERVIEW

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HPA dataset
RNA tissue category:  Expressed in all

Organ

Expression

GTEx dataset
RNA tissue category:  Expressed in all

Organ

Expression



GENE INFORMATION

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Gene name

HSPD1 (HGNC Symbol)

Synonyms

GROEL, HSP60, SPG13

Description

Heat shock 60kDa protein 1 (chaperonin) (HGNC Symbol)

Entrez gene summary

This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun 2010]

Chromosome

2

Cytoband

q33.1

Chromosome location (bp)

197486581 - 197516737

Protein evidence

Evidence at protein level (all genes)

Ensembl

ENSG00000144381 (version 78.38)

Entrez gene

3329

UniProt

P10809 (UniProt - Evidence at protein level)

neXtProt

NX_P10809

Antibodypedia

HSPD1 antibodies


PROTEIN BROWSER

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ENST00000345042
 
ENST00000388968
 
ENST00000418022
 
ENST00000426480
 
ENST00000428204
 
ENST00000430176
 
ENST00000439605
 
ENST00000452200
 
 
 
 


PROTEIN INFORMATION

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Splice variant

Ensembl

UniProt

Protein class

Gene ontology

Length
(aa)

Molecular mass
(kDa)

Signal peptide
(predicted)

Transmembrane regions
(predicted)

HSPD1-001 ENSP00000373620
ENST00000388968
P10809
Show all »
Show » Show » 573 61.1 No 0
HSPD1-006 ENSP00000412717
ENST00000452200
E7EXB4
Show all »
Show » Show » 221 23.8 No 0
HSPD1-009 ENSP00000414446
ENST00000426480
C9JL25
Show all »
Show » Show » 175 19.2 No 0
HSPD1-010 ENSP00000396460
ENST00000428204
C9JCQ4
Show all »
Show » Show » 94 10.3 No 0
HSPD1-011 ENSP00000402478
ENST00000439605
C9JL19
Show all »
Show » Show » 83 9 No 0
HSPD1-012 ENSP00000412227
ENST00000418022
C9J0S9
Show all »
Show » Show » 58 6.4 No 0
HSPD1-013 ENSP00000393670
ENST00000430176
E7ESH4
Show all »
Show » Show » 234 25.2 No 0
HSPD1-201 ENSP00000340019
ENST00000345042
P10809
Show all »
Show » Show » 573 61.1 No 0