AXDND1 axonemal dynein light chain domain containing 1
Gene ID: 126859, updated on 28-Oct-2024Gene type: protein coding
Also known as: C1orf125
- See all available tests in GTR for this gene
- Go to complete Gene record for AXDND1
- Go to Variation Viewer for AXDND1 variants
Summary
Predicted to be involved in manchette assembly. Located in cytoplasm. [provided by Alliance of Genome Resources, Oct 2024]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. GeneReviews: Not available |
Genomic context
- Location:
- 1q25.2
- Sequence:
- Chromosome: 1; NC_000001.11 (179365705..179554735)
- Total number of exons:
- 33
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for AXDND1 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
- RefSeqGeneLink to Nucleotide RefSeqGenes
- 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.