Gene Gene information from NCBI Gene database.
Entrez ID 9537
Gene name Tumor protein p53 inducible protein 11
Gene symbol TP53I11
Synonyms (NCBI Gene)
PIG11
Chromosome 11
Chromosome location 11p11.2
miRNA miRNA information provided by mirtarbase database.
535
miRTarBase ID miRNA Experiments Reference
MIRT000150 hsa-miR-210-3p Luciferase reporter assay 19782034
MIRT1448094 hsa-miR-103a CLIP-seq
MIRT1448095 hsa-miR-107 CLIP-seq
MIRT1448096 hsa-miR-1202 CLIP-seq
MIRT1448097 hsa-miR-1205 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
2
GO ID Ontology Definition Evidence Reference
GO:0008285 Process Negative regulation of cell population proliferation TAS 9305847
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617867 16842 ENSG00000175274
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
O14683
Protein name Tumor protein p53-inducible protein 11 (p53-induced gene 11 protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14936 p53-inducible11 10 188 Tumour protein p53-inducible protein 11 Family
Sequence
Sequence length 189
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
Colon adenocarcinoma Likely benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HYPERTROPHIC CARDIOMYOPATHY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Breast Carcinoma Breast Carcinoma BEFREE 30940320
★☆☆☆☆
Found in Text Mining only
Carcinogenesis Carcinogenesis Pubtator 19096915, 30241046 Associate
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 19096915 Inhibit
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Hepatocellular carcinoma Pubtator 30241046 Associate
★☆☆☆☆
Found in Text Mining only
Liver carcinoma Liver carcinoma BEFREE 12557265, 19333544, 30241046
★☆☆☆☆
Found in Text Mining only
Liver neoplasms Liver neoplasms BEFREE 12557265, 30241046
★☆☆☆☆
Found in Text Mining only
Liver Neoplasms Liver neoplasm Pubtator 19096915, 30241046 Inhibit
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of breast Breast Cancer BEFREE 30940320
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 12579308
★☆☆☆☆
Found in Text Mining only
Stomach Neoplasms Stomach Neoplasms LHGDN 12883691
★☆☆☆☆
Found in Text Mining only