MYRIP myosin VIIA and Rab interacting protein
Gene ID: 25924, updated on 18-Sep-2024Gene type: protein coding
Also known as: SLAC2C; SLAC2-C
- See all available tests in GTR for this gene
- Go to complete Gene record for MYRIP
- Go to Variation Viewer for MYRIP variants
Summary
Predicted to enable actin binding activity and myosin binding activity. Predicted to be involved in positive regulation of insulin secretion. Predicted to be located in actin cytoskeleton; dense core granule; and perinuclear region of cytoplasm. Predicted to be part of exocyst. Predicted to be active in cortical actin cytoskeleton. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genome-wide association of sleep and circadian phenotypes. GeneReviews: Not available | |
| Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia. GeneReviews: Not available | |
| Whole genome association scan for genetic polymorphisms influencing information processing speed. GeneReviews: Not available |
Genomic context
- Location:
- 3p22.1
- Sequence:
- Chromosome: 3; NC_000003.12 (39808914..40260321)
- Total number of exons:
- 20
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for MYRIP 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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