Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
284353
Gene name Gene Name - the full gene name approved by the HGNC.
NTPase KAP family P-loop domain containing 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NKPD1
Synonyms (NCBI Gene) Gene synonyms aliases
-
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.32
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT718649 hsa-miR-759 HITS-CLIP 19536157
MIRT718648 hsa-miR-4514 HITS-CLIP 19536157
MIRT718647 hsa-miR-4692 HITS-CLIP 19536157
MIRT718646 hsa-miR-6515-3p HITS-CLIP 19536157
MIRT718645 hsa-miR-412-3p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
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
HGNC N/A HGNC
Protein
UniProt ID Q17RQ9
Protein name NTPase KAP family P-loop domain-containing protein 1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07693 KAP_NTPase 36 414 KAP family P-loop domain Domain
Sequence
Sequence length 610
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
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Ichthyosis Lamellar Associate 38642798
Lamellar ichthyosis autosomal dominant form Associate 38642798