Gene Gene information from NCBI Gene database.
Entrez ID 25880
Gene name Transmembrane protein 186
Gene symbol TMEM186
Synonyms (NCBI Gene)
C16orf51
Chromosome 16
Chromosome location 16p13.2
Summary This gene encodes a potential transmembrane protein. [provided by RefSeq, Dec 2012]
miRNA miRNA information provided by mirtarbase database.
192
miRTarBase ID miRNA Experiments Reference
MIRT706384 hsa-miR-2392 HITS-CLIP 22927820
MIRT706383 hsa-miR-1976 HITS-CLIP 22927820
MIRT706382 hsa-miR-6790-3p HITS-CLIP 22927820
MIRT706380 hsa-miR-6821-3p HITS-CLIP 22927820
MIRT706381 hsa-miR-3605-5p HITS-CLIP 22927820
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
11
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32320651, 32814053
GO:0005739 Component Mitochondrion HTP 34800366
GO:0005739 Component Mitochondrion IBA
GO:0005739 Component Mitochondrion IDA 32275929
GO:0005739 Component Mitochondrion IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620433 24530 ENSG00000184857
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96B77
Protein name Transmembrane protein 186
Protein function As part of the MCIA complex, required for efficient assembly of the mitochondrial complex I.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14640 TMEM223 52 210 Family
Sequence
Sequence length 213
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
GASTROESOPHAGEAL REFLUX DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Breast Neoplasms Associate 35779338
★☆☆☆☆
Found in Text Mining only