This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq, Feb 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| CNNM4-20-RE | 20 (40 μL) | 200 μL |  |
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| CNNM4-20-OR | 20 (40 μL) | 200 μL |  |
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| CNNM4-20-GO | 20 (40 μL) | 200 μL |  |
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| CNNM4-20-GR | 20 (40 μL) | 200 μL |  |
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| CNNM4-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the ancient conserved domain containing protein family. Members of this protein family contain a cyclin box motif and have structural similarity to the cyclins. The encoded protein may play a role in metal ion transport. Mutations in this gene are associated with Jalili syndrome which consists of cone-rod dystrophy and amelogenesis imperfecta. [provided by RefSeq, Feb 2010]
Gene Symbol : CNNM4
Gene Name : Cyclin and CBS domain divalent metal cation transport mediator 4
Chromosome : CHR 2: 967,609,01-968,118,90
Locus : 2q11.2
Alt. Genes : RBM12
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