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Basic information of NINJ2 :

Official Symbol of Gene NINJ2
Species Homo sapiens
Entrez Gene ID 4815
Official Full Name ninjurin 2
Also known as N/A
Gene Type protein coding
dbXrefs Ensembl:ENSG00000171840 MIM:607297; AllianceGenome:HGNC:7825
Map Location 12p13.33
Variation Type SNP
refSNP ID rs11833579

Sample information of multiple sclerosis:

Detected Sample peripheral blood
Sample Detail N/A
Detected Method ARMS-PCR
Disease MS
Disease subtype RRMS
Population Iranian
Sample Size 410 MS patients/410 healthy controls

Literature information of multiple sclerosis :

Pubmed ID 31292852
Year 2019
Title A single nucleotide polymorphism within Ninjurin 2 is associated with risk of multiple sclerosis

Results of multiple sclerosis :

Risk Type Disease risk
Main Result Negative
Result There were no significant difference in the alleles and genotypes frequencies of rs11833579 between cases and controls.Based on the D’ and r statistics, the mentioned SNPS were not in strong linkage disequilibrium.
Mechanism/Pathway Ninjurin 2 (NINJ2) participates in the process of nerve regeneration after nerve damage.As a protein which regulates the attachment of monocytes to endothelial cells and thus controls the relocation of immune cells to the CNS. Notably, based on the results of co-expression investigations, NINJ2 participates in immune system-associated pathways. Therefore, NINJ2 has prominent roles in nerve regeneration, immune response regulation and development of MS.