- About
- Home
- Introduction
- Statistics
- Programs
- Dignet
- Gene
- GenePair
- BioSummarAI
- Help & Docs
- Documents
- Help
- FAQs
- Links
- Acknowledge
- Disclaimer
- Contact Us
Gene Information
Gene symbol: MBD3
Gene name: methyl-CpG binding domain protein 3
HGNC ID: 6918
Related Genes
| # | Gene Symbol | Number of hits |
| 1 | DNMT1 | 1 hits |
| 2 | DNMT3L | 1 hits |
| 3 | ZFP57 | 1 hits |
Related Sentences
| # | PMID | Sentence |
| 1 | 20738330 | Silver-Russell patients showing a broad range of ICR1 and ICR2 hypomethylation in different tissues. |
| 2 | 20738330 | However, several patients with transient neonatal diabetes mellitus (TNDM), Silver-Russell syndrome (SRS) and Beckwith-Wiedemann syndrome (BWS) exhibiting multilocus hypomethylation (MLH) have meanwhile been described. |
| 3 | 20738330 | Whereas TNDM patients with MLH show clinical symptoms different from carriers with isolated 6q24 aberrations, MLH carriers diagnosed as BWS or SRS present only the syndrome-specific features. |
| 4 | 20738330 | Interestingly, SRS and BWS patients with nearly identical MLH patterns in leukocytes have been identified. |
| 5 | 20738330 | Despite mutation screening of several factors involved in establishment and maintenance of methylation marks including ZFP57, MBD3, DNMT1 and DNMT3L the molecular clue for the ICR1/ICR2 hypomethylation in our patients remained unclear. |