BUD13 BUD13 homolog
Gene ID: 84811, updated on 10-Oct-2024Gene type: protein coding
Also known as: Cwc26; fSAP71
- See all available tests in GTR for this gene
- Go to complete Gene record for BUD13
- Go to Variation Viewer for BUD13 variants
Summary
Enables RNA binding activity. Involved in mRNA splicing, via spliceosome. Located in nucleoplasm. Part of U2-type precatalytic spliceosome. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
A bivariate genome-wide approach to metabolic syndrome: STAMPEED consortium. GeneReviews: Not available | |
A genome-wide association study in the genetic analysis of idiopathic thrombophilia project suggests sex-specific regulation of mitochondrial DNA levels. GeneReviews: Not available | |
Amerindian-specific regions under positive selection harbour new lipid variants in Latinos. GeneReviews: Not available | |
An atlas of genetic influences on human blood metabolites. GeneReviews: Not available | |
Common human genetic variants and HIV-1 susceptibility: a genome-wide survey in a homogeneous African population. GeneReviews: Not available | |
Genetic variants influencing circulating lipid levels and risk of coronary artery disease. GeneReviews: Not available | |
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. GeneReviews: Not available | |
Genome-wide association study identifies common variants associated with circulating vitamin E levels. GeneReviews: Not available | |
Genome-wide association study identifies three common variants associated with serologic response to vitamin E supplementation in men. GeneReviews: Not available | |
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides. GeneReviews: Not available | |
Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci. GeneReviews: Not available | |
Large-scale genome-wide association studies in East Asians identify new genetic loci influencing metabolic traits. GeneReviews: Not available | |
Longitudinal genome-wide association of cardiovascular disease risk factors in the Bogalusa heart study. GeneReviews: Not available | |
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans. GeneReviews: Not available | |
THOC5: a novel gene involved in HDL-cholesterol metabolism. GeneReviews: Not available |
Genomic context
- Location:
- 11q23.3
- Sequence:
- Chromosome: 11; NC_000011.10 (116748173..116772987, complement)
- Total number of exons:
- 10
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for BUD13 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
IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.