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Gene: Tp53inp2 (tumor protein p53 inducible nuclear protein 2) Rattus norvegicus
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Symbol: Tp53inp2
Name: tumor protein p53 inducible nuclear protein 2
Description: Predicted to have ubiquitin binding activity. Predicted to be involved in several processes, including autophagosome assembly; osteoblast differentiation; and ubiquitin-dependent protein catabolic process. Predicted to localize to the autophagosome; cytosol; and nucleus. Orthologous to human TP53INP2 (tumor protein p53 inducible nuclear protein 2); INTERACTS WITH (+)-schisandrin B; (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; 1,2-dimethylhydrazine.
Type: protein-coding
RefSeq Status: PROVISIONAL
Also known as: diabetes and obesity-regulated; LOC362246; Trp53inp2; tumor protein p53-inducible nuclear protein 2
Orthologs:
Latest Assembly: Rnor_6.0 - RGSC Genome Assembly v6.0
Position:
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.03150,910,398 - 150,918,525 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.03157,278,515 - 157,286,642 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.43145,878,005 - 145,886,088 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.13145,783,626 - 145,788,521 (+)NCBI
Celera3142,607,828 - 142,615,961 (+)NCBICelera
Cytogenetic Map3q41NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

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

Sequence

Nucleotide Sequences
Protein Sequences
Transcriptome
Promoters

Strain Variation

Strain Sequence Variants (Rnor 5.0)
Damaging Variants

Additional Information

External Database Links
Nomenclature History
 
More on Tp53inp2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: rn5 rn6
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 735085
Created: 2004-02-05
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.