TMEM132B
protein-coding gene in the species Homo sapiens
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Key Facts
- Subclass of: protein-coding gene[1]
- HomoloGene ID: 28135[2]
- Genomic start: 125671382[3], 125186386[4]
- Genomic end: 125662377[5], 126146917[6]
- Ortholog: Tmem132b[7]
- Encodes: Transmembrane protein 132B[8]
- Found in taxon: Homo sapiens[9]
- Chromosome: human chromosome 12[10]
- Genetic association: amyotrophic lateral sclerosis[11], bipolar disorder[12]
- Strand orientation: forward strand[13]
- Exact match: http://identifiers.org/ncbigene/114795[14]
- Cytogenetic location: 12q24.31-q24.32[15]
- Expressed in: ventricular zone[16], ganglionic eminence[17], endothelial cell[18], middle temporal gyrus[19], Brodmann area 23[20], Brodmann area 46[21], sural nerve[22], superior frontal gyrus[23], prefrontal cortex[24], primary visual cortex[25]