1. Gene
  2. TRAP1 - TNF receptor associated protein 1 Gene

TRAP1 - TNF receptor associated protein 1 Gene

Homo sapiens

Also known as HSP75; HSP 75; HSP90L; TRAP-1

Gene ID: 10131 | Gene type: protein coding

About TRAP1

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:3,658,037-3,717,524 (from NCBI)

This gene has 17 transcripts (splice variants), 210 orthologues and 3 paralogues. Ubiquitous expression in kidney (RPKM 31.7), heart (RPKM 25.6) and 25 other tissues.

Summary

This gene encodes a mitochondrial chaperone protein that is member of the heat shock protein 90 (HSP90) family. The encoded protein has ATPase activity and interacts with tumor necrosis factor type I. This protein may function in regulating cellular stress responses. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2013]

TRAP1 Products(2)

mRNA Protein Name
NM_001272049.2 NP_001258978.1 heat shock protein 75 kDa, mitochondrial isoform 2
NM_016292.3 NP_057376.2 heat shock protein 75 kDa, mitochondrial isoform 1 precursor

TRAP1 Protein Structure

HATPase_c_3

HATPase_c_3: Histidine kinase-, DNA gyrase B-, and HSP90-like ATPase (110 - 223)

HSP90

HSP90: Hsp90 protein (291 - 701)

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  • 704 a.a.
Protein Preferred Names Protein Names

heat shock protein 75 kDa, mitochondrial

TNFR-associated protein 1

Recombinant TRAP1 Proteins

Cat. No. Product Name Accession Purity
HY-P71537 TRAP1 Protein, Human (GST) Q12931 (60S-308E) ≥95%

Related Diseases

Diseases Alias
Cakut

Renal Or Urinary Tract Malformation

Congenital Anomalies Of Kidney And Urinary Tract

Congenital Anomaly Of Kidney And Urinary Tract

Congenital Anomalies Of The Kidney And Urinary Tract

Kidney And Urinary Tract, Anomalies, Congenital

Renal Hypodysplasia, Nonsyndromic, 1

Vacterl Association, X-Linked, With Or Without Hydrocephalus

VACTERLX

X-Linked Vacterl Association

Vacterl-H, X-Linked

Vacterl Association, X-Linked

Vacterl Association, X-Linked With Or Without Hydrocephalus

Vacterl Association X-Linked With Or Without Hydrocephalus

Vacterl Syndrome

Vertebral Anal Tracheoesophageal Esophageal Radial Anomalies

X-Linked Vacterl-H

Vacterl Association

Vacterl Association With Hydrocephalus

Retinitis Pigmentosa 71

RP71

Retinitis Pigmentosa, Type 71

Short-Rib Thoracic Dysplasia 10 With Or Without Polydactyly

SRTD10

Short-Rib Thoracic Dysplasia 10 Without Polydactyly

Short Rib-Polydactyly Syndrome

Vacterl Association

Vater Association

Vater Syndrome

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

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 TRAP1 VGNC VGNC:36283
Macaca mulatta TRAP1 VGNC VGNC:79019
Mus musculus TRAP1 MGD MGI:1915265
Felis catus TRAP1 VGNC VGNC:66507
Rattus norvegicus TRAP1 RGD RGD:1359733
Canis familiaris TRAP1 VGNC VGNC:47776
Others TRAP1 NCBI