Gene Gene information from NCBI Gene database.
Entrez ID 285386
Gene name Tumor protein p63 regulated 1
Gene symbol TPRG1
Synonyms (NCBI Gene)
FAM79B
Chromosome 3
Chromosome location 3q28
miRNA miRNA information provided by mirtarbase database.
87
miRTarBase ID miRNA Experiments Reference
MIRT021515 hsa-miR-145-5p Reporter assay;Microarray 21351259
MIRT756348 hsa-miR-129-5p Western blottingqRT-PCR 37294527
MIRT1450212 hsa-miR-103a CLIP-seq
MIRT1450213 hsa-miR-107 CLIP-seq
MIRT1450214 hsa-miR-1200 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32296183
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm 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.
Q6ZUI0
Protein name Tumor protein p63-regulated gene 1 protein (Protein FAM79B)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF12456 hSac2 65 172 Inositol phosphatase Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in the epidermal layer of the skin. {ECO:0000269|PubMed:18256694}.
Sequence
MSTIGSFEGFQAVSLKQEGDDQPSETDHLSMEEEDPMPRQISRQSSVTESTLYPNPYHQP
YISRKYFATRPGAIETAMEDLKGHVAETSGETIQGFWLLTKIDHWNNEKERILLVTDKTL
LICKYDFIMLSCVQLQRIPLSAVYRICLGKFTFPGMSLDKRQGEGLRIYWGS
PEEQSLLS
RWNPWSTEVPYATFTEHPMKYTSEKFLEICKLSGFMSKLVPAIQNAHKNSTGSGRGKKLM
VLTEPILIETYTGLMSFIGNRNKLGYSLARGSIGF
Sequence length 275
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
15
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
COLOR VISION DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CUTANEOUS SQUAMOUS CELL CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LUNG ADENOCARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
LUNG CANCER 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 Neoplasms Breast neoplasm Pubtator 30961553 Associate
★☆☆☆☆
Found in Text Mining only
Lipoma Lipoma BEFREE 19963137
★☆☆☆☆
Found in Text Mining only
Lipomatosis, Multiple Lipomatosis BEFREE 19963137
★☆☆☆☆
Found in Text Mining only
Squamous Cell Carcinoma of Head and Neck Squamous cell carcinoma Pubtator 37481637 Associate
★☆☆☆☆
Found in Text Mining only