Gene Gene information from NCBI Gene database.
Entrez ID 130827
Gene name Transmembrane protein 182
Gene symbol TMEM182
Synonyms (NCBI Gene)
-
Chromosome 2
Chromosome location 2q12.1
miRNA miRNA information provided by mirtarbase database.
116
miRTarBase ID miRNA Experiments Reference
MIRT1433136 hsa-miR-106a CLIP-seq
MIRT1433137 hsa-miR-106b CLIP-seq
MIRT1433138 hsa-miR-1257 CLIP-seq
MIRT1433139 hsa-miR-1260 CLIP-seq
MIRT1433140 hsa-miR-1260b CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 28514442, 32296183, 33961781
GO:0005886 Component Plasma membrane IEA
GO:0007517 Process Muscle organ development IEA
GO:0014906 Process Myotube cell development involved in skeletal muscle regeneration IEA
GO:0014906 Process Myotube cell development involved in skeletal muscle regeneration ISS
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.
Q6ZP80
Protein name Transmembrane protein 182
Protein function Negatively regulates myogenesis and skeletal muscle regeneration via its association with ITGB1 (By similarity). Modulates ITGB1 activation by decreasing ITGB1-LAMB1 interaction and inhibiting ITGB1-mediated intracellular signaling during myogen
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13903 Claudin_2 15 220 PMP-22/EMP/MP20/Claudin tight junction Family
Sequence
Sequence length 229
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
14
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
ASTHMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
BREAST CARCINOMA 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 30893332 Associate
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Colorectal neoplasm Pubtator 39596218 Associate
★☆☆☆☆
Found in Text Mining only
Glaucoma Glaucoma BEFREE 23349798
★☆☆☆☆
Found in Text Mining only
Other and unspecified reactive psychosis Reactive Psychosis GWASCAT_DG 24132900
★☆☆☆☆
Found in Text Mining only
Psychotic Disorders Psychosis GWASCAT_DG 24132900
★☆☆☆☆
Found in Text Mining only
Squamous cell carcinoma Carcinoma BEFREE 30893332
★☆☆☆☆
Found in Text Mining only
Squamous Cell Carcinoma of Head and Neck Squamous cell carcinoma Pubtator 30893332 Associate
★☆☆☆☆
Found in Text Mining only