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CNNM4 encodes a member of the ancient conserved domain containing protein family. Additionally we are shipping CNNM4 Proteins (7) and many more products for this protein.
Showing 10 out of 40 products:
Human Polyclonal CNNM4 Primary Antibody for IHC (p), WB - ABIN651611
Parry, Mighell, El-Sayed, Shore, Jalili, Dollfus, Bloch-Zupan, Carlos, Carr, Downey, Blain, Mansfield, Shahrabi, Heidari, Aref, Abbasi, Michaelides, Moore, Kirkham, Inglehearn: Mutations in CNNM4 cause Jalili syndrome, consisting of autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta. in American journal of human genetics 2009
Show all 2 references for ABIN651611
Human Polyclonal CNNM4 Primary Antibody for WB - ABIN2783768
Wang, Shi, Yang, Kumar, Li, Run, Su, Scott, Kao, She: Molecular cloning and characterization of a novel gene family of four ancient conserved domain proteins (ACDP). in Gene 2003
these results indicate that CNNM4-dependent Mg(2 (show MUC7 Antibodies)+) efflux suppresses tumor progression by regulating energy metabolism.
The c.1312 dupC mutation of CNNM4 leads to a premature termination of amelogenesis resulting in thin, incompletely mineralized enamel, whereas in dentin, only mineralization is disturbed.
CNNM4 is sorted to the basolateral membrane by the complementary function of AP-1A and AP-1B
Data indicate that a mutation in the cystathionine-beta-synthase (CBS (show CBS Antibodies)) domains of ancient conserved domain protein 4/cyclin M4 CNNM4 completely abrogated their Mg2 (show MUC7 Antibodies)+ efflux functions.
These results demonstrate the crucial importance of Mg(2 (show MUC7 Antibodies)+) extrusion by CNNM4 in organismal and topical regulation of magnesium.
Our case shows a unique combination of NF1 (show NF1 Antibodies) and Jalili syndrome; clinical examination, but also of molecular genetic analysis, which together provide a precise diagnosis.
This work describes the purification and preliminary crystallographic analysis of the CBS (show CBS Antibodies)-pair regulatory domain of the human ancient domain protein 4 (ACDP4), also known as CNNM4.
Identification of CNNM4 as the causative gene for Jalili syndrome, characterized by autosomal-recessive cone-rod dystrophy and amelogenesis imperfecta.
Since CNNM4 is implicated in metal ion transport, cone-rod dystrophy and amelogenesis imperfecta may originate from abnormal ion homeostasis.
these results indicate that CNNM4-dependent Mg(2 (show MCOLN1 Antibodies)+) efflux suppresses tumor progression by regulating energy metabolism.
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.
, metal transporter CNNM4
, metal transporter CNNM4-like
, ancient conserved domain protein 4
, ancient conserved domain-containing protein 4