RTN2
protein-coding gene in the species Homo sapiens
Press Enter · cited answer in seconds
0 sources
Summary
RTN2 is a gene[1]. RTN2 is a type of protein-coding gene[2].
Key Facts
- HomoloGene ID: 32180[3]
- Genomic start: 45988547[4], 45485294[5]
- Genomic end: 46000319[6], 45497055[7]
- Ortholog: Rtn2[8]
- Encodes: Reticulon 2[9], Reticulon 2, isoform CRA_f[10]
- Found in taxon: Homo sapiens[11]
- Chromosome: human chromosome 19[12]
- Genetic association: hereditary spastic paraplegia 12[13]
- Strand orientation: reverse strand[14]
- Cytogenetic location: 19q13.32[15]
- Expressed in: Skeletal muscle tissue of rectus abdominis[16], muscle of thigh[17], gastrocnemius muscle[18], vastus lateralis muscle[19], thoracic diaphragm[20], triceps brachii muscle[21], biceps brachii[22], glutes[23], body of tongue[24], Skeletal muscle tissue of biceps brachii[25]