Gene Gene information from NCBI Gene database.
Entrez ID 90313
Gene name Tumor protein p53 inducible protein 13
Gene symbol TP53I13
Synonyms (NCBI Gene)
DSCP1
Chromosome 17
Chromosome location 17q11.2
miRNA miRNA information provided by mirtarbase database.
5
miRTarBase ID miRNA Experiments Reference
MIRT037401 hsa-miR-744-5p CLASH 23622248
MIRT1448266 hsa-miR-2277-5p CLIP-seq
MIRT1448267 hsa-miR-4706 CLIP-seq
MIRT1448268 hsa-miR-4749-5p CLIP-seq
MIRT1448269 hsa-miR-765 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IDA 14767535
GO:0005737 Component Cytoplasm IEA
GO:0005886 Component Plasma membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NBR0
Protein name Tumor protein p53-inducible protein 13 (Damage-stimulated cytoplasmic protein 1)
Protein function May act as a tumor suppressor. Inhibits tumor cell growth, when overexpressed.
Family and domains
Tissue specificity TISSUE SPECIFICITY: Expressed in heart, placenta, skeletal muscle, testis, brain and lung.
Sequence
MAPPPPSPQLLLLAALARLLGPSEVMAGPAEEAGAHCPESLWPLPPQVSPRVTYTRVSPG
QAEDVTFLYHPCAHPWLKLQLALLAYACMANPSLTPDFSLTQDRPLVLTAWGLALEMAWV
EPAWAAHWLMRRRRRKQRKKKAWIYCESLSGPAPSEPTPGRGRLCRRGCVQALALAFALR
SWRPPGTEVTSQGPRQPSSSGAKRRRLRAALGPQPTRSALRFPSASPGSLKAKQSMAGIP
GRESNAPSVPTVSLLPGAPGGNASSRTEAQVPNGQGSPGGCVCSSQASPAPRAAAPPRAA
RGPTPRTEEAAWAAMALTFLLVLLTLATLCTRLHRNFRRGESIYWGPTADSQDTVAAVLK
RRLLQPSRRVKRSRRRPLLPPTPDSGPEGESSE
Sequence length 393
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
DEVELOPMENTAL DISABILITIES Disgenet
★★☆☆☆
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
Alzheimer Disease Alzheimer disease Pubtator 32233750 Associate
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma Pubtator 36275718 Associate
★☆☆☆☆
Found in Text Mining only
Glioma Glioma Pubtator 36275718 Associate
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 14767535
★☆☆☆☆
Found in Text Mining only
Obesity Obesity Pubtator 24504737 Associate
★☆☆☆☆
Found in Text Mining only