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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Lanosterol synthase
Summary
- UniProt ID
- P48449
- Gene Symbol
-
- LSS
- OSC
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P48449
- PubChem
- P48449
- SwissLipids
- The Human Metabolome Database
- HMDBP00430
- The O-GlcNAc Database
- P48449
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Cataract
- Direct protein sequencing
- Disease variant
- Endoplasmic reticulum
- Hypotrichosis
- Intellectual disability
- Isomerase
- Membrane
- Reference proteome
- Repeat
- Steroid biosynthesis
- Gene Ontology (GO)
| GO Term |
|---|
| endoplasmic reticulum membrane |
| lipid droplet |
| membrane |
| GO Term |
|---|
| lanosterol synthase activity |
Sequence
MTEGTCLRRRGGPYKTEPATDLGRWRLNCERGRQTWTYLQDERAGREQTGLEAYALGLDTKNYFKDLPKAHTAFEGALNGMTFYVGLQAEDGHWTGDYGGPLFLLPGLLITCHVARIPLPAGYREEIVRYLRSVQLPDGGWGLHIEDKSTVFGTALNYVSLRILGVGPDDPDLVRARNILHKKGGAVAIPSWGKFWLAVLNVYSWEGLNTLFPEMWLFPDWAPAHPSTLWCHCRQVYLPMSYCYAVRLSAAEDPLVQSLRQELYVEDFASIDWLAQRNNVAPDELYTPHSWLLRVVYALLNLYEHHHSAHLRQRAVQKLYEHIVADDRFTKSISIGPISKTINMLVRWYVDGPASTAFQEHVSRIPDYLWMGLDGMKMQGTNGSQIWDTAFAIQALLEAGGHHRPEFSSCLQKAHEFLRLSQVPDNPPDYQKYYRQMRKGGFSFSTLDCGWIVSDCTAEALKAVLLLQEKCPHVTEHIPRERLCDAVAVLLNMRNPDGGFATYETKRGGHLLELLNPSEVFGDIMIDYTYVECTSAVMQALKYFHKRFPEHRAAEIRETLTQGLEFCRRQQRADGSWEGSWGVCFTYGTWFGLEAFACMGQTYRDGTACAEVSRACDFLLSRQMADGGWGEDFESCEERRYLQSAQSQIHNTCWAMMGLMAVRHPDIEAQERGVRCLLEKQLPNGDWPQENIAGVFNKSCAISYTSYRNIFPIWALGRFSQLYPERALAGHP
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Activation of gene expression by SREBF (SREBP) | Homo sapiens |
| Cholesterol biosynthesis | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110717 | Warburg micro syndrome 2 | |
| DOID:0110718 | Warburg micro syndrome 3 | |
| DOID:0110719 | Warburg micro syndrome 4 | |
| DOID:3393 | coronary artery disease | |
| DOID:0110881 | holoprosencephaly 1 | |
| DOID:10113 | trypanosomiasis | |
| DOID:1059 | intellectual disability | |
| DOID:10763 | hypertension | |
| DOID:10825 | essential hypertension | |
| DOID:10907 | microcephaly |
