This gene encodes a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1. [provided by RefSeq, Jul 2008]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
GJC2-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
GJC2-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
GJC2-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
GJC2-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
GJC2-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
This gene encodes a gap junction protein. Gap junction proteins are members of a large family of homologous connexins and comprise 4 transmembrane, 2 extracellular, and 3 cytoplasmic domains. This gene plays a key role in central myelination and is involved in peripheral myelination in humans. Defects in this gene are the cause of autosomal recessive Pelizaeus-Merzbacher-like disease-1. [provided by RefSeq, Jul 2008]
Gene Symbol : GJC2
Gene Name : Gap junction protein gamma 2
Chromosome : CHR 1: 228,149,713-228,159,825
Locus : 1q42.13
Alt. Genes : YAF2
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.