DEGS1 delta 4-desaturase, sphingolipid 1
Gene ID: 8560, updated on 17-Sep-2024Gene type: protein coding
Also known as: MLD; DEGS; DES1; Des-1; FADS7; HLD18; MIG15; DEGS-1
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- Go to complete Gene record for DEGS1
- Go to Variation Viewer for DEGS1 variants
Summary
This gene encodes a member of the membrane fatty acid desaturase family which is responsible for inserting double bonds into specific positions in fatty acids. This protein contains three His-containing consensus motifs that are characteristic of a group of membrane fatty acid desaturases. It is predicted to be a multiple membrane-spanning protein localized to the endoplasmic reticulum. Overexpression of this gene inhibited biosynthesis of the EGF receptor, suggesting a possible role of a fatty acid desaturase in regulating biosynthetic processing of the EGF receptor. [provided by RefSeq, Mar 2010]
Associated conditions
See all available tests in GTR for this gene
Description | Tests |
---|---|
Leukodystrophy, hypomyelinating, 18 | See labs |
Genomic context
- Location:
- 1q42.11
- Sequence:
- Chromosome: 1; NC_000001.11 (224183240..224193441)
- Total number of exons:
- 5
Variation
Resource | Links for this gene |
---|---|
ClinVar | Variants reported to ClinVar |
dbVar | Studies and variants |
SNP | Variation Viewer for DEGS1 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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