ALG10B ALG10 alpha-1,2-glucosyltransferase B
Gene ID: 144245, updated on 23-Mar-2024Gene type: protein coding
Also known as: KCR1; ALG10
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- Go to complete Gene record for ALG10B
- Go to Variation Viewer for ALG10B variants
Summary
Enables transferase activity. Involved in positive regulation of inward rectifier potassium channel activity; positive regulation of protein glycosylation; and protein glycosylation. Located in endoplasmic reticulum. Implicated in long QT syndrome 2. [provided by Alliance of Genome Resources, Apr 2022]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin. GeneReviews: Not available | |
| Long QT syndrome 2 | See labs |
Genomic context
- Location:
- 12q12
- Sequence:
- Chromosome: 12; NC_000012.12 (38316687..38329721)
- Total number of exons:
- 4
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for ALG10B variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- MedGenRelated information in MedGen
- 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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