Gene Gene information from NCBI Gene database.
Entrez ID 441027
Gene name Transmembrane protein 150C
Gene symbol TMEM150C
Synonyms (NCBI Gene)
TTN3
Chromosome 4
Chromosome location 4q21.22
Summary This gene encodes a transmembrane protein component of a mechanosensitve ion channel that is activated by mechanical stimuli in various cell types and confers slowly adapting, mechanically activated currents in dorsal root ganglion neurons. Mechanically a
miRNA miRNA information provided by mirtarbase database.
124
miRTarBase ID miRNA Experiments Reference
MIRT1431470 hsa-miR-128 CLIP-seq
MIRT1431471 hsa-miR-148a CLIP-seq
MIRT1431472 hsa-miR-148b CLIP-seq
MIRT1431473 hsa-miR-152 CLIP-seq
MIRT1431474 hsa-miR-198 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0005764 Component Lysosome IEA
GO:0005765 Component Lysosomal membrane IEA
GO:0005765 Component Lysosomal membrane TAS 25608530
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IDA 25608530
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
617292 37263 ENSG00000249242
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
B9EJG8
Protein name Transmembrane protein 150C (Tentonin 3)
Protein function Nonselective cationic channel with high permeability to Ca(2+). Component of a mechanosensitive cation channel, confers mechanically activated (MA) currents with slow inactivation kinetics. May contribute to proprioception. {ECO:0000250|UniProtK
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10277 Frag1 8 218 Frag1/DRAM/Sfk1 family Family
Sequence
Sequence length 249
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEMENTIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations