Gene Gene information from NCBI Gene database.
Entrez ID 153396
Gene name Transmembrane protein 161B
Gene symbol TMEM161B
Synonyms (NCBI Gene)
FLB3342PRO1313
Chromosome 5
Chromosome location 5q14.3
miRNA miRNA information provided by mirtarbase database.
170
miRTarBase ID miRNA Experiments Reference
MIRT026084 hsa-miR-196a-5p Sequencing 20371350
MIRT665818 hsa-miR-190a-5p HITS-CLIP 23824327
MIRT665817 hsa-miR-190b HITS-CLIP 23824327
MIRT665816 hsa-miR-4307 HITS-CLIP 23824327
MIRT665815 hsa-miR-4446-5p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
7
GO ID Ontology Definition Evidence Reference
GO:0002027 Process Regulation of heart rate IEA
GO:0002027 Process Regulation of heart rate ISS
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane ISS
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621178 28483 ENSG00000164180
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NDZ6
Protein name Transmembrane protein 161B
Protein function Essential for maintaining normal cardiac rhythm in the developing heart and for neonatal survival (By similarity). Inhibits potassium and calcium currents in the cardiomyocytes, this assists in timely action potential repolarization and thereby
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10268 Tmemb_161AB 2 485 Predicted transmembrane protein 161AB Family
Sequence
Sequence length 487
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
12
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
HYPERTENSION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
IRRITABLE BOWEL SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Attention Deficit Disorder with Hyperactivity Associate 31575856
★☆☆☆☆
Found in Text Mining only
Bipolar Disorder Associate 33828235
★☆☆☆☆
Found in Text Mining only
Depressive Disorder Associate 33828235
★☆☆☆☆
Found in Text Mining only
Esophageal Neoplasms Associate 34046994
★☆☆☆☆
Found in Text Mining only
Esophageal Squamous Cell Carcinoma Associate 34046994
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Inhibit 34046994
★☆☆☆☆
Found in Text Mining only
Mood Disorders Associate 33828235
★☆☆☆☆
Found in Text Mining only
Multiple Myeloma Associate 37227248
★☆☆☆☆
Found in Text Mining only
Pulpitis Associate 37208635
★☆☆☆☆
Found in Text Mining only