The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
ZNF778-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
ZNF778-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
ZNF778-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
ZNF778-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
ZNF778-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
The protein encoded by this gene is a member of the krueppel C2H2-type zinc-finger protein family, and it contains one KRAB domain and eighteen C2H2-type zinc fingers. This gene is a candidate gene for autism and variable cognitive impairment in the 16q24.3 microdeletion syndrome. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2011]
Gene Symbol : ZNF778
Gene Name : Zinc finger protein 778
Chromosome : CHR 16: 892,021,11-892,344,52
Locus : 16q24.3
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.