- About
- Home
- Introduction
- Statistics
- Programs
- Dignet
- Gene
- GenePair
- BioSummarAI
- Help & Docs
- Documents
- Help
- FAQs
- Links
- Acknowledge
- Disclaimer
- Contact Us
Gene Information
Gene symbol: CD226
Gene name: CD226 molecule
HGNC ID: 16961
Synonyms: DNAM-1, DNAM1, PTA1, TLiSA1
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | ADAD1 | 1 hits |
| 2 | AFF3 | 1 hits |
| 3 | C12orf30 | 1 hits |
| 4 | CAPS | 1 hits |
| 5 | CAPSL | 1 hits |
| 6 | CLEC16A | 1 hits |
| 7 | CLECL1 | 1 hits |
| 8 | FCRL3 | 1 hits |
| 9 | IFIH1 | 1 hits |
| 10 | IL17C | 1 hits |
| 11 | KIF5A | 1 hits |
| 12 | PTPN2 | 1 hits |
| 13 | SCGB1A1 | 1 hits |
| 14 | SCGB3A2 | 1 hits |
| 15 | SH2B3 | 1 hits |
| 16 | SMARCE1 | 1 hits |
| 17 | SUOX | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 18987646 | Two of these seven SNPs showed evidence of association with multiple sclerosis; that is rs12708716 from the CLEC16A gene (P=1.6 x 10(-16)) and rs763361 from the CD226 gene (P=5.4 x 10(-8)). |
| 2 | 20089178 | Allelic variants in the PHTF1-PTPN22, C12orf30 and CD226 regions as candidate susceptibility factors for the type 1 diabetes in the Estonian population. |
| 3 | 20508602 | The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis. |
| 4 | 20508602 | Three SNPs were found to be associated with MS: rs1678542 in KIF5A (P=0.001, odds ratio (OR)=1.13, 95% confidence interval (CI)=1.05-1.23); rs3184504 in SH2B3 (P=0.00001, OR=1.19, 95% CI=1.10-1.27) and rs763361 in CD226 (P=0.00007, OR=1.16, 95%CI=1.08-1.25). |
| 5 | 20508602 | The autoimmune disease-associated KIF5A, CD226 and SH2B3 gene variants confer susceptibility for multiple sclerosis. |
| 6 | 20508602 | Three SNPs were found to be associated with MS: rs1678542 in KIF5A (P=0.001, odds ratio (OR)=1.13, 95% confidence interval (CI)=1.05-1.23); rs3184504 in SH2B3 (P=0.00001, OR=1.19, 95% CI=1.10-1.27) and rs763361 in CD226 (P=0.00007, OR=1.16, 95%CI=1.08-1.25). |
| 7 | 22403184 | Our results reflect the importance of monocyte (and their derivatives, macrophage and dendritic cell) gene expression in human T1D and support the candidacy of several genes as causal factors in autoimmune pancreatic beta-cell destruction, including AFF3, CD226, CLECL1, DEXI, FKRP, PRKD2, RNLS, SMARCE1 and SUOX, in addition to the recently described GPR183 (EBI2) gene. |
| 8 | 22654555 | In particular, we discuss recent efforts aimed at refining diseases associations found within the HLA complex and implicating HLA class I as well as HLA-DPB1 loci. |
| 9 | 22654555 | We summarize data regarding non-HLA genes such as PTPN22, CTLA4, CD40, TSHR and TG which have been extensively studied in respect to their role in GD. |
| 10 | 22654555 | We review recent findings implicating variants of FCRL3 (gene for FC receptor-like-3 protein), SCGB3A2 (gene for secretory uteroglobin-related protein 1- UGRP1) as well as other unverified possible candidate genes for GD selected through their documented association with type 1 diabetes mellitus: Tenr-IL2-IL21, CAPSL (encoding calcyphosine-like protein), IFIH1(gene for interferon-induced helicase C domain 1), AFF3, CD226 and PTPN2. |