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Gene: Anp32e (acidic nuclear phosphoprotein 32 family member E) Rattus norvegicus
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Symbol: Anp32e
Name: acidic nuclear phosphoprotein 32 family member E
Description: Predicted to have histone binding activity and phosphatase inhibitor activity. Predicted to be involved in histone exchange. Predicted to localize to the Swr1 complex and cytoplasmic vesicle. Orthologous to human ANP32E (acidic nuclear phosphoprotein 32 family member E); INTERACTS WITH (S)-10-[(DIMETHYLAMINO)METHYL]-4-ETHYL-4,9-DIHYDROXY-1H-PYRANO[3',4':6,7]INOLIZINO[1,2-B]-QUINOLINE-3,14(4H,12H)-DIONE; 2,4-dinitrotoluene; 2,6-dinitrotoluene.
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: acidic (leucine-rich) nuclear phosphoprotein 32 family, member E; acidic leucine-rich nuclear phosphoprotein 32 family member E; LOC361999
Orthologs:
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.02198,040,573 - 198,057,005 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02217,530,730 - 217,546,919 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.42190,715,685 - 190,730,204 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.12190,678,438 - 190,692,957 (+)NCBI
Celera2176,001,553 - 176,015,902 (+)NCBICelera
Cytogenetic Map2q34NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated
RGD Disease Portals

Genomics

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

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome
Promoters

Strain Variation

Strain Sequence Variants (Rnor 5.0)

Additional Information

External Database Links
Nomenclature History
 
More on Anp32e
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1310611
Created: 2005-01-12
Species: Rattus norvegicus
Last Modified: 2019-04-23
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.