Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
152519
Gene name Gene Name - the full gene name approved by the HGNC.
NIPA like domain containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NIPAL1
Synonyms (NCBI Gene) Gene synonyms aliases
NIPA3, NPAL1, SLC57A3
Chromosome Chromosome number
4
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
4p12
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT026452 hsa-miR-192-5p Microarray 19074876
MIRT043429 hsa-miR-331-3p CLASH 23622248
MIRT667216 hsa-miR-6890-3p HITS-CLIP 23824327
MIRT667215 hsa-miR-6887-3p HITS-CLIP 23824327
MIRT667214 hsa-miR-4667-3p 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:0000139 Component Golgi membrane IEA
GO:0005794 Component Golgi apparatus IEA
GO:0005794 Component Golgi apparatus ISS
GO:0006811 Process Monoatomic ion transport IEA
GO:0015095 Function Magnesium ion transmembrane transporter activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620340 27194 ENSG00000163293
Protein
UniProt ID Q6NVV3
Protein name Magnesium transporter NIPA3 (NIPA-like protein 1) (Non-imprinted in Prader-Willi/Angelman syndrome region protein 3)
Protein function Acts as a Mg(2+) transporter. Can also transport other divalent cations such as Fe(2+), Sr(2+), Ba(2+), Mn(2+), Cu(2+) and Co(2+) but to a much less extent than Mg(2+) (By similarity).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF05653 Mg_trans_NIPA 66 360 Magnesium transporter NIPA Family
Tissue specificity TISSUE SPECIFICITY: Expressed in the pancreatic islets. {ECO:0000269|PubMed:32439805}.
Sequence
Sequence length 410
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Miscellaneous transport and binding events
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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
Breast Cancer Breast cancer N/A N/A GWAS
Gout Gout N/A N/A GWAS
Uterine Fibroids Uterine fibroids N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Nasopharyngeal Carcinoma Associate 31289279