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Gene: TP53INP1 (tumor protein p53 inducible nuclear protein 1) Homo sapiens
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Symbol: TP53INP1
Name: tumor protein p53 inducible nuclear protein 1
Description: Predicted to have antioxidant activity. Involved in autophagic cell death; positive regulation of autophagy; and positive regulation of transcription, DNA-templated. Localizes to the autophagosome; cytosol; and nucleus; INTERACTS WITH (-)-demecolcine; 17alpha-ethynylestradiol; 17beta-estradiol.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: DKFZp434M1317; FLJ22139; p53-dependent damage-inducible nuclear protein 1; p53-inducible p53DINP1; p53DINP1; SIP; stress-induced protein; Teap; TP53DINP1; TP53INP1A; TP53INP1B; tumor protein p53-inducible nuclear protein 1
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl894,925,972 - 94,949,378 (-)Ensembl
GRCh38894,925,972 - 94,949,378 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37895,938,200 - 95,961,615 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36896,007,377 - 96,030,767 (-)NCBINCBI36hg18NCBI36
Build 34896,007,376 - 96,030,767NCBI
Celera892,123,395 - 92,146,810 (-)NCBI
Cytogenetic Map8q22.1NCBI
HuRef891,146,079 - 91,169,530 (-)NCBIHuRef
CHM1_1895,978,531 - 96,001,887 (-)NCBICHM1_1
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
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
 
More on TP53INP1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1349699
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2020-01-14
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.