DHRSX dehydrogenase/reductase X-linked
Gene ID: 207063, updated on 18-Nov-2024Gene type: protein coding
Also known as: DHRSY; CDG1DD; DHRS5X; DHRS5Y; DHRSXY; SDR7C6; CXorf11; SDR46C1
- See all available tests in GTR for this gene
- Go to complete Gene record for DHRSX
- Go to Variation Viewer for DHRSX variants
Summary
Predicted to enable oxidoreductase activity. Involved in positive regulation of autophagy. Located in extracellular region. [provided by Alliance of Genome Resources, Nov 2024]
Genomic context
- Location:
- Xp22.33 and Yp11.2
- Sequence:
- Chromosome: X; NC_000023.11 (2219506..2500976, complement)
- Chromosome: Y; NC_000024.10 (2219506..2500976, complement)
- Total number of exons:
- 7
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for DHRSX 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.