CUX2
protein-coding gene in the species Homo sapiens
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CUX2
Summary
CUX2 is a gene[1].
Key Facts
- CUX2's instance of is recorded as gene[2].
- CUX2 is a type of protein-coding gene[3].
- CUX2's HomoloGene ID is recorded as 22426[4].
- CUX2's genomic start is recorded as 111471828[5].
- CUX2's genomic start is recorded as 111034165[6].
- CUX2's genomic end is recorded as 111350554[7].
- CUX2's genomic end is recorded as 111788358[8].
- CUX2's ortholog is recorded as Cux2[9].
- CUX2's ortholog is recorded as Cux2[10].
- CUX2's ortholog is recorded as cux2b[11].
- CUX2's encodes is recorded as Cut like homeobox 2[12].
- CUX2's found in taxon is recorded as Homo sapiens[13].
- CUX2's chromosome is recorded as human chromosome 12[14].
- CUX2's genetic association is recorded as coronary artery disease[15].
- CUX2's genetic association is recorded as type-1 diabetes[16].
- CUX2's strand orientation is recorded as forward strand[17].
- CUX2's exact match is recorded as http://identifiers.org/ncbigene/23316[18].
- CUX2's cytogenetic location is recorded as 12q24.11-q24.12[19].
- CUX2's expressed in is recorded as middle temporal gyrus[20].
- CUX2's expressed in is recorded as buccal mucosa cell[21].
- CUX2's expressed in is recorded as Brodmann area 23[22].
- CUX2's expressed in is recorded as endothelial cell[23].
- CUX2's expressed in is recorded as lateral nuclear group of thalamus[24].
- CUX2's expressed in is recorded as Epithelium of choroid plexus[25].
- CUX2's expressed in is recorded as primary visual cortex[26].