======= MBD1 ======= == Gene Information == * **Official Symbol**: MBD1 * **Official Name**: methyl-CpG binding domain protein 1 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=4152|4152]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9UIS9|Q9UIS9]] * **Interactions**: [[https://thebiogrid.org/search.php?search=MBD1&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20MBD1|Open PubMed]] * **OMIM**: [[https://omim.org/entry/156535|Open OMIM]] == Function Summary == * **Entrez Summary**: The protein encoded by this gene is a member of a family of nuclear proteins related by the presence of a methyl-CpG binding domain (MBD). These proteins are capable of binding specifically to methylated DNA, and some members can also repress transcription from methylated gene promoters. This protein contains multiple domains: MBD at the N-terminus that functions both in binding to methylated DNA and in protein interactions; several CXXC-type zinc finger domains that mediate binding to non-methylated CpG dinucleotides; transcriptional repression domain (TRD) at the C-terminus that is involved in transcription repression and in protein interactions. Numerous alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Feb 2011]. * **UniProt Summary**: N/A |MBD| |zf-CXXC| |double-stranded methylated DNA binding| |negative regulation of astrocyte differentiation| |methylation-dependent chromatin silencing| |regulation of DNA methylation| |negative regulation of glial cell differentiation| |methyl-CpG binding| |regulation of astrocyte differentiation| |negative regulation of gliogenesis| |response to cocaine| |chromatin organization involved in negative regulation of transcription| |chromatin silencing| |regulation of glial cell differentiation| |chromatin organization involved in regulation of transcription| |response to anesthetic| |negative regulation of gene expression, epigenetic| |nuclear matrix| |response to alkaloid| |regulation of gliogenesis| |response to estradiol| |gene silencing| |response to ammonium ion| |regulation of gene expression, epigenetic| |nuclear chromatin| |aging| |negative regulation of neurogenesis| |response to xenobiotic stimulus| |negative regulation of nervous system development| |negative regulation of cell development| |regulation of DNA metabolic process| |covalent chromatin modification| |chromatin binding| |nuclear speck| |transcription by RNA polymerase II| |response to nutrient levels| |heart development| |response to extracellular stimulus| |transcription, DNA-templated| |nucleic acid-templated transcription| |RNA biosynthetic process| |chromatin organization| |negative regulation of cell differentiation| |regulation of neurogenesis| |zinc ion binding| |response to lipid| |negative regulation of transcription by RNA polymerase II| |circulatory system development| |response to hormone| |response to organic cyclic compound| |regulation of nervous system development| |regulation of cell development| |negative regulation of developmental process| |response to organonitrogen compound| |neuron differentiation| |response to drug| |chromosome organization| |response to nitrogen compound| |nucleobase-containing compound biosynthetic process| |heterocycle biosynthetic process| |aromatic compound biosynthetic process| |negative regulation of transcription, DNA-templated| |negative regulation of multicellular organismal process| |negative regulation of nucleic acid-templated transcription| |negative regulation of RNA biosynthetic process| |organic cyclic compound biosynthetic process| |negative regulation of RNA metabolic process| |negative regulation of cellular macromolecule biosynthetic process| |negative regulation of nucleobase-containing compound metabolic process| |DNA binding| |negative regulation of macromolecule biosynthetic process| |response to endogenous stimulus| |negative regulation of cellular biosynthetic process| |generation of neurons| |negative regulation of biosynthetic process| |response to oxygen-containing compound| |DNA-binding transcription factor activity, RNA polymerase II-specific| |neurogenesis| |cellular nitrogen compound biosynthetic process| |RNA metabolic process| |cellular macromolecule biosynthetic process| |negative regulation of gene expression| |macromolecule biosynthetic process| |regulation of cell differentiation| |gene expression| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp28|Pimelic-diphenylamide-106 5μM R00 exp28]]|-2.45| |[[:results:exp2|5-Fluorouracil 20μM R00 exp2]]|-2.05| |[[:results:exp417|Tubastatin-A 2.5μM R07 exp417]]|-1.97| |[[:results:exp29|Rapamycin 1μM R00 exp29]]|-1.87| |[[:results:exp216|Erlotinib 10μM R05 exp216]]|-1.73| |[[:results:exp365|I-BRD9 4μM R07 exp365]]|-1.72| |[[:results:exp108|Vinblastine 0.2μM R03 exp108]]|-1.71| |[[:results:exp362|GSK-J4 1μM R07 exp362]]|1.97| |[[:results:exp400|Senexin-A 25μM R07 exp400]]|2.24| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 0/726 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/25| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/15| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/14| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/7| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 16447 * **Expression level (log2 read counts)**: 6.9 {{:chemogenomics:nalm6 dist.png?nolink |}}