This gene encodes a predicted transmembrane protein with a perinuclear Golgi-like distribution in fibroblasts. Mutations in this gene are associated with the autosomal recessive disorder congenital disorder of glycosylation, type IIk. Knockdown of this gene's expression causes decreased sialylation in HEK cells and suggests this gene plays a role in terminal Golgi glycosylation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| TMEM165-20-RE | 20 (40 μL) | 200 μL |  |
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| TMEM165-20-OR | 20 (40 μL) | 200 μL |  |
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| TMEM165-20-GO | 20 (40 μL) | 200 μL |  |
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| TMEM165-20-GR | 20 (40 μL) | 200 μL |  |
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| TMEM165-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a predicted transmembrane protein with a perinuclear Golgi-like distribution in fibroblasts. Mutations in this gene are associated with the autosomal recessive disorder congenital disorder of glycosylation, type IIk. Knockdown of this gene's expression causes decreased sialylation in HEK cells and suggests this gene plays a role in terminal Golgi glycosylation. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2012]
Gene Symbol : TMEM165
Gene Name : Transmembrane protein 165
Chromosome : CHR 4: 553,959,12-554,533,96
Locus : 4q12
Alt. Genes : LRPPRC
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