CNKSR3 CNKSR family member 3
Gene ID: 154043, updated on 2-Nov-2024Gene type: protein coding
Also known as: CNK3; MAGI1; CNK3/IPCEF1
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- Go to complete Gene record for CNKSR3
- Go to Variation Viewer for CNKSR3 variants
Summary
Predicted to be involved in negative regulation of ERK1 and ERK2 cascade; negative regulation of peptidyl-serine phosphorylation; and positive regulation of sodium ion transport. Predicted to act upstream of or within positive regulation of sodium ion transmembrane transporter activity. Predicted to be located in apical plasma membrane and cytoplasm. [provided by Alliance of Genome Resources, Nov 2024]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations. GeneReviews: Not available | |
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2. GeneReviews: Not available |
Genomic context
- Location:
- 6q25.2
- Sequence:
- Chromosome: 6; NC_000006.12 (154387515..154510685, complement)
- Total number of exons:
- 15
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for CNKSR3 variants |
Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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