FAM135B family with sequence similarity 135 member B
Gene ID: 51059, updated on 5-Mar-2024Gene type: protein coding
Also known as: C8ORFK32
- See all available tests in GTR for this gene
- Go to complete Gene record for FAM135B
- Go to Variation Viewer for FAM135B variants
Summary
Predicted to be involved in cellular lipid metabolic process. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
A genome-wide association study of inflammatory biomarker changes in response to fenofibrate treatment in the Genetics of Lipid Lowering Drug and Diet Network. GeneReviews: Not available | |
Common genetic variation and performance on standardized cognitive tests. GeneReviews: Not available | |
Genome-wide association study of chronic periodontitis in a general German population. GeneReviews: Not available |
Genomic context
- Location:
- 8q24.23
- Sequence:
- Chromosome: 8; NC_000008.11 (138130023..138497730, complement)
- Total number of exons:
- 30
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for FAM135B 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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