Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11270
Gene name Gene Name - the full gene name approved by the HGNC.
Nurim
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NRM
Synonyms (NCBI Gene) Gene synonyms aliases
NRM29
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6p21.33
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene contains transmembrane domains and resides within the inner nuclear membrane, where it is tightly associated with the nucleus. This protein shares homology with isoprenylcysteine carboxymethyltransferase enzymes. Alternati
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT439154 hsa-let-7c-5p 3'LIFE 25074381
MIRT439154 hsa-let-7c-5p 3'LIFE 25074381
MIRT1194265 hsa-miR-1236 CLIP-seq
MIRT1194266 hsa-miR-1245b-3p CLIP-seq
MIRT1194267 hsa-miR-1253 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005515 Function Protein binding IPI 25416956, 31515488, 32296183
GO:0005635 Component Nuclear envelope IDA 10402458
GO:0005637 Component Nuclear inner membrane IEA
GO:0008150 Process Biological_process ND
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
620017 8003 ENSG00000137404
Protein
UniProt ID Q8IXM6
Protein name Nurim (Nuclear envelope membrane protein) (Nuclear rim protein)
Family and domains
Sequence
MAPALLLIPAALASFILAFGTGVEFVRFTSLRPLLGGIPESGGPDARQGWLAALQDRSIL
APLAWDLGLLLLFVGQHSLMAAERVKAWTSRYFGVLQRSLYVACTALALQLVMRYWEPIP
KGPVLWEARAEPWATWVPLLCFVLHVISWLLIFSILLVFDYAELMGLKQVYYHVLGLGEP
LALKSPRALRLFSHLRHPVCVELLTVLWVVPTLGTDRLLLAFLLTLYLGLAHGLDQQDLR
YLRAQLQRKLHLLSRPQDGEAE
Sequence length 262
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Rheumatoid arthritis Rheumatoid Arthritis rs587776843 17804836
Associations from Text Mining
Disease Name Relationship Type References
Astrocytoma Associate 38307919
Cardiovascular Diseases Associate 33256815
Fetal Growth Retardation Associate 33256815
Glioma Associate 38307919
Hyperlipoproteinemia Type II Associate 28473662
Multiple Sclerosis Associate 21654846
Ventricular Remodeling Associate 33256815