Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
26471
Gene name Gene Name - the full gene name approved by the HGNC.
Nuclear protein 1, transcriptional regulator
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NUPR1
Synonyms (NCBI Gene) Gene synonyms aliases
COM1, P8
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16p11.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018204 hsa-miR-335-5p Microarray 18185580
MIRT022819 hsa-miR-124-3p Microarray 18668037
MIRT040412 hsa-miR-615-3p CLASH 23622248
MIRT755577 hsa-miR-4443 Luciferase reporter assay, Western blotting, qRT-PCR 36269411
MIRT1551917 hsa-miR-3160-5p CLIP-seq
Transcription factors
Transcription factor Regulation Reference
ATF4 Activation 19946894
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002526 Process Acute inflammatory response IEA
GO:0003677 Function DNA binding IDA 11056169, 18690848
GO:0003682 Function Chromatin binding IEA
GO:0003713 Function Transcription coactivator activity IMP 11940591
GO:0005515 Function Protein binding IPI 11940591, 16300740, 16478804, 18690848, 19723804, 20181828, 28720707, 32814053
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614812 29990 ENSG00000176046
Protein
UniProt ID O60356
Protein name Nuclear protein 1 (Candidate of metastasis 1) (Protein p8)
Protein function Transcription regulator that converts stress signals into a program of gene expression that empowers cells with resistance to the stress induced by a change in their microenvironment. Thereby participates in the regulation of many processes name
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10195 Phospho_p8 21 77 DNA-binding nuclear phosphoprotein p8 Family
Tissue specificity TISSUE SPECIFICITY: Widely expressed, with high levels in liver, pancreas, prostate, ovary, colon, thyroid, spinal cord, trachea and adrenal gland, moderate levels in heart, placenta, lung, skeletal muscle, kidney, testis, small intestine, stomach and lym
Sequence
Sequence length 82
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  
  Transcriptional misregulation in cancer  
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Heart failure Heart Failure, Diastolic 29556499 ClinVar
Pancreatitis Pancreatitis 16822955 ClinVar
Crohn Disease Crohn Disease GWAS
Inflammatory Bowel Disease Inflammatory Bowel Disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 36400857, 38167084
Alzheimer Disease Associate 38537674
Breast Neoplasms Associate 20847343, 22858377, 22938721
Carcinogenesis Associate 22938721
Carcinoma Hepatocellular Associate 26173068, 26350749, 27336713, 29763915
Cell Transformation Neoplastic Associate 33920455
Endometrial Neoplasms Associate 34817046
Hand Foot and Mouth Disease Associate 36269411
Huntington Disease Associate 26056083
Idiopathic Pulmonary Fibrosis Associate 38203769