CMSS1 cms1 ribosomal small subunit homolog
Gene ID: 84319, updated on 17-Jun-2024Gene type: protein coding
Also known as: C3orf26
- See all available tests in GTR for this gene
- Go to complete Gene record for CMSS1
- Go to Variation Viewer for CMSS1 variants
Summary
Enables RNA binding activity. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci. GeneReviews: Not available | |
| Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. GeneReviews: Not available |
Genomic context
- Location:
- 3q12.1
- Sequence:
- Chromosome: 3; NC_000003.12 (99817862..100181732)
- Total number of exons:
- 11
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for CMSS1 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- Variation ViewerRelated Variants
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