Skip to content
GeneQ18035352· pop 7· linked from 11 articles

Also known as CAP43, CMT4D, DRG-1, DRG1, GC4, HMSNL, NDR1, NMSL

Protein NDRG1 is a protein that in humans is encoded by the NDRG1 gene.

Gene data

NDRG1
Name
N-myc downstream regulated 1
Type
protein-coding
Position
133,237,175–133,302,022 (−)
Aliases
CAP43, CMT4D, DRG-1, DRG1, GC4, HMSNL, NDR1, NMSL, PROXY1, RIT42
RefSeq RNA
NM_001135242.2, NM_001258432.2, NM_001258433.2, NM_001374844.1, NM_001374845.1
RefSeq protein
NP_001128714.1, NP_001245361.1, NP_001245362.1, NP_001361773.1, NP_001361774.1

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 involved in stress responses, hormone responses, cell growth, and differentiation. The encoded protein is necessary for p53-mediated caspase activation and apoptosis. Mutations in this gene are a cause of Charcot-Marie-Tooth disease type 4D, and expression of this gene may be a prognostic indicator for several types of cancer. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, May 2012].

via MyGene.info

Gene · Ensembl

N-myc downstream regulated 1

Symbol
NDRG1
Biotype
Protein coding
Organism
Homo sapiens
Location
8:133,237,171-133,302,022
Strand
Reverse (−)
Assembly
GRCh38
View on Ensembl →

via Ensembl · EMBL-EBI

Wikidata facts

Show 5 more facts
HomoloGene ID
55953
genomic end
134314265
genomic start
133237175
cytogenetic location
8q24.22
Sources (5)

via Wikidata · CC0

~5 min read

Article

7 sections
Contents
  • Gene
  • Role in cancer
  • Functions in DNA repair and aging
  • Role in immune system
  • References
  • Further reading
  • External links

Protein NDRG1 is a protein that in humans is encoded by the NDRG1 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 involved in stress responses, hormone responses, cell growth, and differentiation. Mutations in this gene have been reported to be causative the autosomal-recessive version of Charcot-Marie-Tooth disease known as CMT4D.

Available in 7 languages

via Wikidata sitelinks · CC0

Connections

Categories