This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| DNAJC30-20-RE | 20 (40 μL) | 200 μL |  |
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| DNAJC30-20-OR | 20 (40 μL) | 200 μL |  |
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| DNAJC30-20-GO | 20 (40 μL) | 200 μL |  |
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| DNAJC30-20-GR | 20 (40 μL) | 200 μL |  |
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| DNAJC30-20-AQ | 20 (40 μL) | 200 μL |  |
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This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. [provided by RefSeq, Jul 2008]
Gene Symbol : DNAJC30
Gene Name : DnaJ heat shock protein family (Hsp40) member C30
Chromosome : CHR 7: 736,834,50-736,809,17
Locus : 7q11.23
Alt. Genes : CEBPZ
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