Gene Gene information from NCBI Gene database.
Entrez ID 153339
Gene name Transmembrane protein 167A
Gene symbol TMEM167A
Synonyms (NCBI Gene)
TMEM167kish
Chromosome 5
Chromosome location 5q14.2
miRNA miRNA information provided by mirtarbase database.
1860
miRTarBase ID miRNA Experiments Reference
MIRT016234 hsa-miR-548b-3p Sequencing 20371350
MIRT020966 hsa-miR-155-5p Proteomics 20584899
MIRT032496 hsa-let-7b-5p Proteomics 18668040
MIRT038333 hsa-miR-130b-5p CLASH 23622248
MIRT037214 hsa-miR-877-5p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005794 Component Golgi apparatus IDA 19942856
GO:0005794 Component Golgi apparatus IEA
GO:0009306 Process Protein secretion IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
620000 28330 ENSG00000174695
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8TBQ9
Protein name Protein kish-A (Transmembrane protein 167) (Transmembrane protein 167A)
Protein function Involved in the early part of the secretory pathway.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF06842 DUF1242 10 44 Protein of unknown function (DUF1242) Family
Sequence
MSAIFNFQSLLTVILLLICTCAYIRSLAPSLLDRNKTGLLGIFWKCARIGERKSPYVAVC
CIVMAFSILFIQ
Sequence length 72
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
5
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
ANDROGENETIC ALOPECIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
COLORECTAL CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GASTRIC CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
GASTRIC 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
Glioma Glioma BEFREE 30506943
★☆☆☆☆
Found in Text Mining only
Pancreatic Neoplasms Pancreatic neoplasm Pubtator 26045837 Associate
★☆☆☆☆
Found in Text Mining only