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Details
- Instance of
- gene
- Subclass of
- protein-coding gene
- chromosome
- human chromosome 9
- cytogenetic location
- 9p24.1-p23
- expressed in
- right hemisphere of cerebellum, C1 segment, ganglionic eminence, Brodmann area 9, prefrontal cortex, right frontal lobe, anterior cingulate cortex, Descending thoracic aorta, rectum, hypothalamus
- found in taxon
- Homo sapiens
- genetic association
- epilepsy, obesity, myopia, restless legs syndrome, type 2 diabetes, focal epilepsy
- genomic end
- 10612723, 10613002
- genomic start
- 8314246, 8314246
- HomoloGene ID
- 88669
- strand orientation
- reverse strand
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