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Gene: Ahsa2 (activator of HSP90 ATPase homolog 2) Rattus norvegicus
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Symbol: Ahsa2
Name: activator of HSP90 ATPase homolog 2
Description: Predicted to have ATPase activator activity; Hsp90 protein binding activity; and chaperone binding activity. Predicted to be involved in positive regulation of ATPase activity. Orthologous to human AHSA2P (activator of HSP90 ATPase homolog 2, pseudogene); INTERACTS WITH 2,4-dinitrotoluene; 2,6-dinitrotoluene; bisphenol A.
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: activator of 90 kDa heat shock protein ATPase homolog 2; activator of heat shock protein ATPase homolog 2; activator of heat shock protein ATPase homolog 2 (yeast); AHA1, activator of heat shock protein ATPase 2; AHA1, activator of heat shock protein ATPase homolog 2; AHA1, activator of heat shock protein ATPase homolog 2 (yeast); LOC305577
Orthologs:
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.014108,262,795 - 108,274,000 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl14108,265,207 - 108,273,938 (-)Ensembl
Rnor_5.014105,098,652 - 105,111,031 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.414104,424,340 - 104,435,511 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.114104,445,383 - 104,454,723 (-)NCBI
Celera1496,451,164 - 96,462,335 (-)NCBICelera
Cytogenetic Map14q22NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - curated
References - uncurated

Genomics

Comparative Map Data
Position Markers
QTLs in Region (Rnor_6.0)
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome
Promoters

Strain Variation

Strain Sequence Variants (Rnor 6.0)

Additional Information

External Database Links
Nomenclature History
 
More on Ahsa2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1307171
Created: 2005-01-12
Species: Rattus norvegicus
Last Modified: 2019-08-20
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.