CNNM4 (cyclin and CBS domain divalent metal cation transport mediator 4)

2015-08-01  

Identity

HGNC
LOCATION
2q11.2
LOCUSID
ALIAS
ACDP4
FUSION GENES

Other Information

Locus ID:

NCBI: 26504
MIM: 607805
HGNC: 105
Ensembl: ENSG00000158158

Variants:

dbSNP: 26504
ClinVar: 26504
TCGA: ENSG00000158158
COSMIC: CNNM4

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000158158ENST00000377075Q6P4Q7

Expression (GTEx)

0
5
10
15
20
25
30
35
40
45

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
381493262024Dimerization of the CNNM extracellular domain.1
381493262024Dimerization of the CNNM extracellular domain.1
363540012023Novel CNNM4 variant and clinical features of Jalili syndrome.1
363540012023Novel CNNM4 variant and clinical features of Jalili syndrome.1
349289372021CNNM proteins selectively bind to the TRPM7 channel to stimulate divalent cation entry into cells.13
349289372021CNNM proteins selectively bind to the TRPM7 channel to stimulate divalent cation entry into cells.13
320223892020Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort.3
320223892020Expanding the genotypic spectrum of Jalili syndrome: Novel CNNM4 variants and uniparental isodisomy in a north American patient cohort.3
313472852019A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations.6
313472852019A novel pathogenic missense variant in CNNM4 underlying Jalili syndrome: Insights from molecular dynamics simulations.6
293222532018Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1.6
294212942018Jalili Syndrome: Cross-sectional and Longitudinal Features of Seven Patients With Cone-Rod Dystrophy and Amelogenesis Imperfecta.4
294216022018Report of two unrelated families with Jalili syndrome and a novel nonsense heterozygous mutation in CNNM4 gene.4
293222532018Identification of a mutation in CNNM4 by whole exome sequencing in an Amish family and functional link between CNNM4 and IQCB1.6
294212942018Jalili 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/meetings/case-report-explorer/