Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
222698
Gene name Gene Name - the full gene name approved by the HGNC.
NFKB activating protein like
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NKAPL
Synonyms (NCBI Gene) Gene synonyms aliases
C6orf194, bA424I5.1
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT663507 hsa-miR-873-3p HITS-CLIP 23313552
MIRT684694 hsa-miR-6867-5p HITS-CLIP 23313552
MIRT663506 hsa-miR-3672 HITS-CLIP 23313552
MIRT663505 hsa-miR-6864-3p HITS-CLIP 23313552
MIRT663504 hsa-miR-6818-5p HITS-CLIP 23313552
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003682 Function Chromatin binding IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0007283 Process Spermatogenesis 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 Q5M9Q1
Protein name NKAP-like protein
Protein function Transcriptional repressor of Notch-mediated signaling. Required for spermatogenesis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15692 NKAP 109 204 Family
PF06047 Nkap_C 293 394 NF-kappa-B-activating protein C-terminal domain Domain
Sequence
MPPVSRSSYSEDIVGSRRRRRSSSGSPPSPQSRCSSWDGCSRSHSRGREGLRPPWSELDV
GALYPFSRSGSRGRLPRFRNYAFASSWSTSYSGYRYHRHCYAEERQSAEDYEKEESHRQR
RLKERERIGELGAPEVWGPSPKFPQLDSDEHTPVEDEEEVTHQKSSSSDSNSEEHRKKKT
SRSRNKKKRKNKSSKRKHRKYSDS
DSNSESDTNSDSDDDKKRVKAKKKKKKKKHKTKKKK
NKKTKKESSDSSCKDSEEDLSEATWMEQPNVADTMDLIGPEAPIIHTSQDEKPLKYGHAL
LPGEGAAMAEYVKAGKRIPRRGEIGLTSEEIGSFECSGYVMSGSRHRRMEAVRLRKENQI
YSADEKRALASFNQEERRKRESKILASFREMVHK
KTKEKDDK
Sequence length 402
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
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Arthritis Rheumatoid Associate 23223422
Neoplasms Associate 28427185
Stomach Neoplasms Associate 29923336