ORMDL2 (ORMDL sphingolipid biosynthesis regulator 2)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 29095 |
| Gene name | ORMDL sphingolipid biosynthesis regulator 2 |
| Gene symbol | ORMDL2 |
| Synonyms (NCBI Gene) |
HSPC160MST095MSTP095adoplin-2
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| Chromosome | 12 |
| Chromosome location | 12q13.2 |
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miRNA
miRNA information provided by mirtarbase database.
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Gene ontology (GO)
Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Protein
Protein information from UniProt database.
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UniProt ID
Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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Q53FV1 | ||||||||||
| Protein name | ORM1-like protein 2 (Adoplin-2) | ||||||||||
| Protein function | Plays an essential role in the homeostatic regulation of sphingolipid de novo biosynthesis by modulating the activity of the serine palmitoyltransferase (SPT) in response to ceramide levels (PubMed:20182505). When complexed to SPT, the binding o | ||||||||||
| Family and domains |
Pfam
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| Tissue specificity | TISSUE SPECIFICITY: Widely expressed. Expressed in adult and fetal heart, brain, lung, liver, skeletal muscle and kidney. Expressed in adult pancreas and placenta and in fetal spleen abd thymus. {ECO:0000269|PubMed:12093374}. | ||||||||||
| Sequence | |||||||||||
| Sequence length | 153 | ||||||||||
| Interactions | View interactions | ||||||||||
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Pathways
Pathway information has different metabolic/signaling pathways associated with genes.
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Related Genes
Genes most often co-reported with ORMDL2 across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to ORMDL2 (see Related Genes above), that are NOT already directly curated for ORMDL2 itself -- a lead worth checking, not a confirmed association.
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