Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 26504
MIM: 607805
HGNC: 105
Ensembl: ENSG00000158158
Variants:
dbSNP: 26504
ClinVar: 26504
TCGA: ENSG00000158158
COSMIC: CNNM4
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000158158 | ENST00000377075 | Q6P4Q7 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38149326 | 2024 | Dimerization of the CNNM extracellular domain. | 1 |
| 38149326 | 2024 | Dimerization of the CNNM extracellular domain. | 1 |
| 36354001 | 2023 | Novel CNNM4 variant and clinical features of Jalili syndrome. | 1 |
| 36354001 | 2023 | Novel CNNM4 variant and clinical features of Jalili syndrome. | 1 |
| 34928937 | 2021 | CNNM proteins selectively bind to the TRPM7 channel to stimulate divalent cation entry into cells. | 13 |
| 34928937 | 2021 | CNNM proteins selectively bind to the TRPM7 channel to stimulate divalent cation entry into cells. | 13 |
| 32022389 | 2020 | Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort. | 3 |
| 32022389 | 2020 | Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort. | 3 |
| 31347285 | 2019 | A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations. | 6 |
| 31347285 | 2019 | A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations. | 6 |
| 29322253 | 2018 | Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1. | 6 |
| 29421294 | 2018 | Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta. | 4 |
| 29421602 | 2018 | Report of two unrelated families with Jalili syndrome and a novel nonsense heterozygous mutation in CNNM4 gene. | 4 |
| 29322253 | 2018 | Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1. | 6 |
| 29421294 | 2018 | Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta. | 4 |
Citation
Dessen P
CNNM4 (cyclin and CBS domain divalent metal cation transport mediator 4)
Atlas Genet Cytogenet Oncol Haematol. 2015-08-01
Online version: http://atlasgeneticsoncology.org/gene/55382/cnnm4-(cyclin-and-cbs-domain-divalent-metal-cation-transport-mediator-4)
