======= MEOX2 ======= == Gene Information == * **Official Symbol**: MEOX2 * **Official Name**: mesenchyme homeobox 2 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=4223|4223]] * **UniProt**: [[https://www.uniprot.org/uniprot/P50222|P50222]] * **Interactions**: [[https://thebiogrid.org/search.php?search=MEOX2&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20MEOX2|Open PubMed]] * **OMIM**: [[https://omim.org/entry/600535|Open OMIM]] == Function Summary == * **Entrez Summary**: This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease. [provided by RefSeq, Jul 2008]. * **UniProt Summary**: Mesodermal transcription factor that plays a key role in somitogenesis and is required for sclerotome development (By similarity). Activates expression of CDKN1A and CDKN2A in endothelial cells, acting as a regulator of vascular cell proliferation. While it activates CDKN1A in a DNA-dependent manner, it activates CDKN2A in a DNA-independent manner (PubMed:22206000). May have a regulatory role when quiescent vascular smooth muscle cells reenter the cell cycle. {ECO:0000250|UniProtKB:P32443, ECO:0000269|PubMed:22206000}. |Homeobox| |somite specification| |negative regulation of cell migration involved in sprouting angiogenesis| |segment specification| |negative regulation of sprouting angiogenesis| |negative regulation of blood vessel endothelial cell migration| |regulation of cell migration involved in sprouting angiogenesis| |negative regulation of endothelial cell migration| |embryonic pattern specification| |somitogenesis| |negative regulation of epithelial cell migration| |regulation of sprouting angiogenesis| |somite development| |regulation of blood vessel endothelial cell migration| |roof of mouth development| |segmentation| |RNA polymerase II distal enhancer sequence-specific DNA binding| |negative regulation of angiogenesis| |negative regulation of blood vessel morphogenesis| |negative regulation of vasculature development| |skeletal muscle tissue development| |skeletal muscle organ development| |regulation of endothelial cell migration| |appendage development| |limb development| |anterior/posterior pattern specification| |regulation of epithelial cell migration| |negative regulation of cell migration| |negative regulation of cell motility| |striated muscle tissue development| |regulation of angiogenesis| |muscle organ development| |muscle tissue development| |negative regulation of cellular component movement| |angiogenesis| |regulation of vasculature development| |negative regulation of locomotion| |regionalization| |blood circulation| |circulatory system process| |nuclear speck| |blood vessel morphogenesis| |sequence-specific DNA binding| |pattern specification process| |DNA-binding transcription activator activity, RNA polymerase II-specific| |muscle structure development| |blood vessel development| |RNA polymerase II proximal promoter sequence-specific DNA binding| |vasculature development| |cardiovascular system development| |chordate embryonic development| |embryo development ending in birth or egg hatching| |tube morphogenesis| |DNA-binding transcription factor activity| |tube development| |regulation of cell migration| |circulatory system development| |anatomical structure formation involved in morphogenesis| |regulation of cell motility| |negative regulation of developmental process| |embryo development| |regulation of locomotion| |regulation of cellular component movement| |regulation of anatomical structure morphogenesis| |epithelium development| |negative regulation of multicellular organismal process| |positive regulation of transcription by RNA polymerase II| |positive regulation of transcription, DNA-templated| |DNA-binding transcription factor activity, RNA polymerase II-specific| |positive regulation of nucleic acid-templated transcription| |positive regulation of RNA biosynthetic process| |positive regulation of RNA metabolic process| |tissue development| |positive regulation of nucleobase-containing compound metabolic process| |positive regulation of macromolecule biosynthetic process| |system process| |positive regulation of cellular biosynthetic process| |positive regulation of gene expression| |positive regulation of biosynthetic process| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp222|Betulinic acid 10 to 15μM on day4 R05 exp222]]|-2| |[[:results:exp277|Curcumin 6.5μM R06 exp277]]|-1.76| |[[:results:exp244|SB743921 0.001μM R05 exp244]]|2.02| |[[:results:exp94|Nocodazole 0.1μM R03 exp94]]|2.04| |[[:results:exp33|Rotenone 2μM R00 exp33]]|2.16| |[[:results:exp24|Nocodazole 0.2μM R00 exp24]]|2.33| |[[:results:exp208|Vinblastine 0.015μM R05 exp208]]|2.52| |[[:results:exp256|HMS-I1 10μM R06 exp256]]|3.09| |[[:results:exp93|DABN racemic mixture R03 exp93]]|3.32| |[[:results:exp111|R-DABN 8μM R03 exp111]]|3.75| No correlation found to any other genes in chemogenomics. Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 16197 * **Expression level (log2 read counts)**: -4.27 {{:chemogenomics:nalm6 dist.png?nolink |}}