CNNM4 抗体
(Cyclin M4 (CNNM4))
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].
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Latest Publications for our CNNM4 抗体
: "Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta." in: American journal of human genetics, Vol. 84, Issue 2, pp. 266-73, (2009) (PubMed).
Aliases for CNNM4 抗体
cyclin and CBS domain divalent metal cation transport mediator 4 (CNNM4) 抗体cyclin M4 (CpipJ_CPIJ006743) 抗体
cyclin and CBS domain divalent metal cation transport mediator 4 (cnnm4) 抗体
cyclin M4 (CNNM4) 抗体
cyclin M4 (Cnnm4) 抗体
cyclin and CBS domain divalent metal cation transport mediator 4 (Cnnm4) 抗体
5430430O18Rik 抗体
ACDP4 抗体
Acdp4 抗体
DKFZp468E0110 抗体
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