Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
65009
Gene name Gene Name - the full gene name approved by the HGNC.
NDRG family member 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
NDRG4
Synonyms (NCBI Gene) Gene synonyms aliases
BDM1, SMAP-8, SMAP8
Chromosome Chromosome number
16
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
16q21
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 is required for cell cycle progression and survival in primary astrocytes an
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT612052 hsa-miR-8485 HITS-CLIP 23313552
MIRT519153 hsa-miR-4789-3p HITS-CLIP 23313552
MIRT612052 hsa-miR-8485 HITS-CLIP 23824327
MIRT612051 hsa-miR-329-3p HITS-CLIP 23824327
MIRT612050 hsa-miR-362-3p 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:0001947 Process Heart looping ISS
GO:0003674 Function Molecular_function ND
GO:0005515 Function Protein binding IPI 25416956
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005737 Component Cytoplasm IDA 12755708
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614463 14466 ENSG00000103034
Protein
UniProt ID Q9ULP0
Protein name Protein NDRG4 (Brain development-related molecule 1) (N-myc downstream-regulated gene 4 protein) (Vascular smooth muscle cell-associated protein 8) (SMAP-8)
Protein function Contributes to the maintenance of intracerebral BDNF levels within the normal range, which is necessary for the preservation of spatial learning and the resistance to neuronal cell death caused by ischemic stress (By similarity). May enhance gro
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF03096 Ndr 8 290 Ndr family Domain
Tissue specificity TISSUE SPECIFICITY: Expressed predominantly in brain and heart (at protein level). In the brain, detected in astrocytes. Isoform 1 and isoform 2 are only expressed in brain. Isoform 3 is expressed in both heart and brain. Up-regulated in glioblastoma mult
Sequence
Sequence length 352
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Schizophrenia Schizophrenia rs13447324, rs387906932, rs387906933, rs863223354, rs863223355, rs776061422, rs863223349, rs748809996, rs759748655, rs863223353, rs863223350, rs863223356, rs781821239, rs863223348, rs863223346
View all (12 more)
29483656
Unknown
Disease term Disease name Evidence References Source
Achromatopsia achromatopsia GenCC
Associations from Text Mining
Disease Name Relationship Type References
Adenoma Associate 23450047
Adrenocortical Carcinoma Associate 33667214
Carcinogenesis Inhibit 25749388
Carcinogenesis Associate 26515606
Carcinoma Pancreatic Ductal Inhibit 33298240
Colitis Inhibit 25749388
Colitis Ulcerative Inhibit 25749388
Colorectal Neoplasms Associate 24993691, 25538088, 26515606, 27114416, 29775793, 30263958, 32467348, 33504902, 33858496, 33890711, 34621892, 35477541, 35963995, 38224931
Colorectal Neoplasms Inhibit 25749388
Fibromatosis Congenital Generalized Associate 25241110