Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
57447
Gene name Gene Name - the full gene name approved by the HGNC.
NDRG family member 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NDRG2
Synonyms (NCBI Gene) Gene synonyms aliases
SYLD
Chromosome Chromosome number
14
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
14q11.2
Summary Summary of gene provided in NCBI Entrez Gene.
This gene is a member of the N-myc downregulated gene family which belongs to the alpha/beta hydrolase superfamily. The protein encoded by this gene is a cytoplasmic protein that may play a role in neurite outgrowth. This gene may be involved in glioblast
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT006183 hsa-miR-650 Immunohistochemistry, Luciferase reporter assay, qRT-PCR, Western blot 21352815
MIRT006183 hsa-miR-650 Immunohistochemistry, Luciferase reporter assay, qRT-PCR, Western blot 21352815
MIRT006183 hsa-miR-650 Immunohistochemistry, Luciferase reporter assay, qRT-PCR, Western blot 21352815
MIRT021510 hsa-miR-145-5p Reporter assay;Microarray 21351259
MIRT736634 hsa-miR-576-3p qRT-PCR, ELISA 32592365
Transcription factors
Transcription factor Regulation Reference
WT1 Activation 17688410
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001818 Process Negative regulation of cytokine production IEA
GO:0003674 Function Molecular_function ND
GO:0005515 Function Protein binding IPI 21217774
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
605272 14460 ENSG00000165795
Protein
UniProt ID Q9UN36
Protein name Protein NDRG2 (N-myc downstream-regulated gene 2 protein) (Protein Syld709613)
Protein function Contributes to the regulation of the Wnt signaling pathway. Down-regulates CTNNB1-mediated transcriptional activation of target genes, such as CCND1, and may thereby act as tumor suppressor. May be involved in dendritic cell and neuron different
PDB 2XMQ , 2XMR , 2XMS
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03096 Ndr 40 318 Ndr family Domain
Tissue specificity TISSUE SPECIFICITY: Highly expressed in brain, heart, skeletal muscle and salivary gland, and moderately in kidney and liver. Expressed in dendritic cells, but not in other blood cells. Expression levels are low in pancreatic and liver cancer tissues; abs
Sequence
Sequence length 371
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Cataract Cataract, Pseudoaphakia rs118203965, rs118203966, rs104893685, rs121908938, rs104894175, rs121909048, rs28937573, rs121909049, rs121909050, rs74315488, rs80358200, rs80358203, rs121434643, rs56141211, rs132630322
View all (150 more)
22043305
Colonic neoplasms Malignant tumor of colon, Colonic Neoplasms rs267607789, rs774277300, rs781222233, rs1060502734, rs1060503333, rs1339238483 15059925
Unknown
Disease term Disease name Evidence References Source
Psoriasis Psoriasis GWAS
Associations from Text Mining
Disease Name Relationship Type References
Acromegaly Inhibit 28390436
Adenocarcinoma Associate 17935612
Adenocarcinoma of Lung Associate 27072586
Adenoma Inhibit 17935612
Adenomatous Polyposis Coli Associate 19237607
Alzheimer Disease Associate 22043305
Arthritis Rheumatoid Associate 30096164
Brain Ischemia Associate 23451161
Breast Neoplasms Inhibit 21226903, 25256221
Breast Neoplasms Associate 21338239, 22647880, 27400234, 28423695