Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
153396
Gene name Gene Name - the full gene name approved by the HGNC.
Transmembrane protein 161B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TMEM161B
Synonyms (NCBI Gene) Gene synonyms aliases
FLB3342, PRO1313
Chromosome Chromosome number
5
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
5q14.3
miRNA miRNA information provided by mirtarbase database.
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 information of associated ontologies with gene provided by GO database.
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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
621178 28483 ENSG00000164180
Protein
UniProt ID 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
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Diabetes Type 2 diabetes N/A N/A GWAS
Hypertension Hypertension (confirmatory factor analysis Factor 12) N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Mental Depression Major depressive disorder N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Attention Deficit Disorder with Hyperactivity Associate 31575856
Bipolar Disorder Associate 33828235
Depressive Disorder Associate 33828235
Esophageal Neoplasms Associate 34046994
Esophageal Squamous Cell Carcinoma Associate 34046994
Lymphatic Metastasis Inhibit 34046994
Mood Disorders Associate 33828235
Multiple Myeloma Associate 37227248
Pulpitis Associate 37208635