Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
8715
Gene name Gene Name - the full gene name approved by the HGNC.
Nucleolar protein 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NOL4
Synonyms (NCBI Gene) Gene synonyms aliases
CT125, HRIHFB2255, NOLP
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18q12.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT016812 hsa-miR-335-5p Microarray 18185580
MIRT025082 hsa-miR-181a-5p Microarray 17612493
MIRT612725 hsa-miR-129-5p HITS-CLIP 23824327
MIRT612723 hsa-miR-4755-3p HITS-CLIP 23824327
MIRT612724 hsa-miR-1202 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:0003723 Function RNA binding TAS 9813152
GO:0005515 Function Protein binding IPI 24722188, 25416956, 32296183
GO:0005634 Component Nucleus IEA
GO:0005730 Component Nucleolus IEA
GO:0005730 Component Nucleolus TAS 9813152
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
603577 7870 ENSG00000101746
Protein
UniProt ID O94818
Protein name Nucleolar protein 4 (Nucleolar-localized protein)
Family and domains
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in fetal brain, adult brain and testis. {ECO:0000269|PubMed:9813152}.
Sequence
MESERDMYRQFQDWCLRTYGDSGKTKTVTRKKYERIVQLLNGSESSSTDNAKFKFWVKSK
GFQLGQPDEVRGGGGGAKQVLYVPVKTTDGVGVDEKLSLRRVAVVEDFFDIIYSMHVETG
PNGEQIRKHAGQKRTYKAISESYAFLPREAVTRFLMSCSECQKRMHLNPDGTDHKDNGKP
PTLVTSMIDYNMPITMAYMKHMKLQLLNSQQDEDESSIESDEFDMSDSTRMSAVNSDLSS
NLEERMQSPQNLHGQQDDDSAAESFNGNETLGHSSIASGGTHSREMGDSNSDGKTGLEQD
EQPLNLSDSPLSAQLTSEYRIDDHNSNGKNKYKNLLISDLKMEREARENGSKSPAHSYSS
YDSGKNESVDRGAEDLSLNRGDEDEDDHEDHDDSEKVNETDGVEAERLKAFNMFVRLFVD
ENLDRMVPISKQPKEKIQAIIDSCRRQFPEYQERARKRIRTYLKSCRRMKRSGFEMSRPI
PSHLTSAVAESILASACESESRNAAKRMRLERQQDESAPADKQCKPEATQATYSTSAVPG
SQDVLYINGNGTYSYHSYRGLGGGLLNLNDASSSGPTDLSMKRQLATSSGSSSSSNSRPQ
LSPTEINAVRQLVAGYRESAAFLLRSADELENLILQQN
Sequence length 638
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, Mild obesity-related type 2 diabetes N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Mental Depression Major depressive disorder 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
Breast Neoplasms Associate 39199284
Carcinoma Pancreatic Ductal Associate 31956659
Endometrial Neoplasms Associate 32074080, 37352078
Head and Neck Neoplasms Associate 24337411
Neoplasms Associate 18381458, 24337411
Prostatic Neoplasms Associate 25733303
Small Cell Lung Carcinoma Associate 34065612, 37399175
Squamous Cell Carcinoma of Head and Neck Associate 24337411
Uterine Cervical Neoplasms Associate 18381458