Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
154215
Gene name Gene Name - the full gene name approved by the HGNC.
Sodium/potassium transporting ATPase interacting 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NKAIN2
Synonyms (NCBI Gene) Gene synonyms aliases
FAM77B, NKAIP2, TCBA, TCBA1
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q22.31
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a transmembrane protein that interacts with the beta subunit of a sodium/potassium-transporting ATPase. A chromosomal translocation involving this gene is a cause of lymphoma. Alternative splicing results in multiple transcript variants
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT017569 hsa-miR-335-5p Microarray 18185580
MIRT1186022 hsa-miR-1224-3p CLIP-seq
MIRT1186023 hsa-miR-1260 CLIP-seq
MIRT1186024 hsa-miR-1260b CLIP-seq
MIRT1186025 hsa-miR-1280 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0002028 Process Regulation of sodium ion transport IBA
GO:0005886 Component Plasma membrane IEA
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
609758 16443 ENSG00000188580
Protein
UniProt ID Q5VXU1
Protein name Sodium/potassium-transporting ATPase subunit beta-1-interacting protein 2 (Na(+)/K(+)-transporting ATPase subunit beta-1-interacting protein 2) (Protein FAM77B) (T-cell lymphoma breakpoint-associated target protein 1)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05640 NKAIN 1 207 Na,K-Atpase Interacting protein Family
Tissue specificity TISSUE SPECIFICITY: Expressed in fetal brain. Weakly expressed in adult brain and thymus. Not expressed in any other normal tissue examined. {ECO:0000269|PubMed:11979551}.
Sequence
Sequence length 208
Interactions View interactions
<
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
Biliary Atresia Biliary atresia N/A N/A GWAS
Celiac disease Celiac disease N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Metabolic Syndrome Metabolic syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Neoplasms Inhibit 27588475
Neuroblastoma Associate 24205241
Pancreatic Neoplasms Associate 28381166
Prostatic Neoplasms Inhibit 27588475
Schizophrenia Associate 34099189