Gene Gene information from NCBI Gene database.
Entrez ID 729533
Gene name Family with sequence similarity 72 member A
Gene symbol FAM72A
Synonyms (NCBI Gene)
LMPIPUgenep17
Chromosome 1
Chromosome location 1q32.1
miRNA miRNA information provided by mirtarbase database.
118
miRTarBase ID miRNA Experiments Reference
MIRT038312 hsa-miR-130b-5p CLASH 23622248
MIRT037238 hsa-miR-877-5p CLASH 23622248
MIRT986838 hsa-let-7a CLIP-seq
MIRT986839 hsa-let-7b CLIP-seq
MIRT986840 hsa-let-7c CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183
GO:0005737 Component Cytoplasm IEA
GO:0005739 Component Mitochondrion IEA
GO:0005829 Component Cytosol IBA
GO:0005829 Component Cytosol IDA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614710 24044 ENSG00000196550
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5TYM5
Protein name Protein FAM72A (Latent membrane protein 1-induced protein) (LMP1-induced protein) (LMPIP)
Protein function May play a role in the regulation of cellular reactive oxygen species metabolism. May participate in cell growth regulation.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14976 FAM72 5 149 FAM72 protein Family
Tissue specificity TISSUE SPECIFICITY: May be up-regulated in malignant colon cancers, compared to normal colon and colon adenomas. Expression is also elevated in other common cancer types, including breast, lung, uterus, and ovary. {ECO:0000269|PubMed:18676834}.
Sequence
Sequence length 149
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
VENOUS THROMBOEMBOLISM 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
Carcinogenesis Carcinogenesis Pubtator 36868233 Associate
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 18676834 Stimulate
★☆☆☆☆
Found in Text Mining only
Dementia Dementia BEFREE 30390010
★☆☆☆☆
Found in Text Mining only
Hemophilia B Hemophilia BEFREE 8573375
★☆☆☆☆
Found in Text Mining only
Hereditary Breast and Ovarian Cancer Syndrome Hereditary breast and ovarian cancer syndrome Pubtator 18676834 Stimulate
★☆☆☆☆
Found in Text Mining only
Lymphoma Lymphoma BEFREE 30261551
★☆☆☆☆
Found in Text Mining only
Lymphoma, Non-Hodgkin Non-Hodgkin lymphoma BEFREE 12010812, 28072889
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of stomach Stomach Neoplasms BEFREE 11973654
★☆☆☆☆
Found in Text Mining only
Malignant Neoplasms Malignant Neoplasm BEFREE 19513564, 29907572
★☆☆☆☆
Found in Text Mining only
Nasopharyngeal carcinoma Nasopharyngeal Carcinoma BEFREE 21317926
★☆☆☆☆
Found in Text Mining only