Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10408
Gene name Gene Name - the full gene name approved by the HGNC.
MYCN opposite strand
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
MYCNOS
Synonyms (NCBI Gene) Gene synonyms aliases
MYCN-AS1, N-CYM, NCYM, NYCM
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2p24.3
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is transcribed in antisense to the v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog gene (MYCN). It is thought to encode a small, novel protein that stabilizes MYCN, prevents apoptosis, and promotes cell proliferation. T
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 24391509
GO:0005634 Component Nucleus IDA 24391509
GO:0005737 Component Cytoplasm IDA 24391509
GO:0007275 Process Multicellular organism development TAS 1419902
GO:0008284 Process Positive regulation of cell population proliferation IMP 24391509
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605374 16911 ENSG00000233718
Protein
UniProt ID P40205
Protein name N-cym protein (N-myc opposite strand)
Protein function Regulates stability of MYCN in neuroblastoma cells by inhibiting GSK3B-mediated MYCN phosphorylation. Inhibits GSK3B activity by promoting its phosphorylation at 'Ser-9' (PubMed:24391509).
Family and domains
Tissue specificity TISSUE SPECIFICITY: Expressed in the neuronal cells of the cerebrum and cerebellum, spermatocytes of the testis, pancreatic cells and also the heart. Expressed in both primary and metastatic neuroblastomas and in thyroid tumors (at protein level). Express
Sequence
MQHPPCEPGNCLSLKEKKITEGSGGVCWGGETDASNPAPALTACCAAEREANVEQGLAGR
LLLCNYERRVVRRCKIAGRGRAPLGTRPLDVSSFKLKEEGRPPCLKINK
Sequence length 109
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Feingold syndrome FEINGOLD SYNDROME 1 rs104893646, rs104893647, rs104893648, rs121913667, rs113994115, rs1558534266, rs574660186, rs1553370260, rs1553370918, rs759103701, rs367962377, rs1553370963, rs754137452, rs780080562, rs1572220856
Glioblastoma Glioblastoma rs121913500, rs886042842, rs1555138291, rs1558518449, rs1567176006, rs1558650888 26619011
Medulloblastoma Medulloblastoma rs1589970134, rs587776578, rs587776579, rs17847577, rs111033171, rs80359604, rs80358785, rs80358814, rs863224925, rs1555950011, rs1554231278, rs926177767, rs759412460, rs1564032829, rs761911009 26619011
Unknown
Disease term Disease name Evidence References Source
Pancreatic adenocarcinoma Adenocarcinoma of pancreas PDAC patients with high expression of PSMA6 having a significantly shorter overall survival rate. 26619011 ClinVar, CBGDA
Neuroticism Neuroticism GWAS
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Renal Cell Associate 31180525
Neuroblastoma Associate 25880909, 25896758, 34289065
Personality Disorders Associate 25880909
Retinoblastoma Associate 33270844