SPRYD7 SPRY domain containing 7
Gene ID: 57213, updated on 19-Sep-2024Gene type: protein coding
Also known as: CLLD6; C13orf1
- See all available tests in GTR for this gene
- Go to complete Gene record for SPRYD7
- Go to Variation Viewer for SPRYD7 variants
Genomic context
- Location:
- 13q14.2
- Sequence:
- Chromosome: 13; NC_000013.11 (49912702..49936340, complement)
- Total number of exons:
- 6
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for SPRYD7 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.