CTNND2
protein-coding gene in the species Homo sapiens
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Summary
CTNND2 is a gene[1]. CTNND2 is known by 4 alternative names across languages and contexts.[2]
Key Facts
- Subclass of: protein-coding gene[3]
- HomoloGene ID: 55574[4]
- Genomic start: 10971952[5], 10971836[6]
- Genomic end: 11904155[7], 11904446[8]
- Ortholog: Ctnnd2[9], ctnnd2b[10], ctnnd2a[11], p120ctn[12]
- Encodes: Catenin delta 2[13], Catenin delta-2[14]
- Found in taxon: Homo sapiens[15]
- Chromosome: human chromosome 5[16]
- Genetic association: amyotrophic lateral sclerosis[17], myopia[18]
- Strand orientation: reverse strand[19]
- Exact match: http://identifiers.org/ncbigene/1501[20]
- Cytogenetic location: 5p15.2[21]
- Expressed in: prefrontal cortex[22], amygdala[23], putamen[24], right frontal lobe[25], postcentral gyrus[26], internal globus pallidus[27], caudate nucleus[28], dorsolateral prefrontal cortex[29], ganglionic eminence[30], ventricular zone[31]