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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Platelet-activating factor acetylhydrolase IB subunit beta
Summary
- UniProt ID
- P43034
- Gene Symbol
-
- PAFAH1B1
- LIS1
- MDCR
- MDS
- PAFAHA
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- P43034
- PubChem
- P43034
- The Human Metabolome Database
- HMDBP00556
- The O-GlcNAc Database
- P43034
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Alternative splicing
- Coiled coil
- Cytoskeleton
- Developmental protein
- Differentiation
- Disease variant
- Lipid degradation
- Lissencephaly
- Membrane
- Microtubule
- Mitosis
- Neurogenesis
- Nucleus
- Phosphoprotein
- Reference proteome
- Repeat
- Transport
- WD repeat
- Gene Ontology (GO)
Sequence
MVLSQRQRDELNRAIADYLRSNGYEEAYSVFKKEAELDVNEELDKKYAGLLEKKWTSVIRLQKKVMELESKLNEAKEEFTSGGPLGQKRDPKEWIPRPPEKYALSGHRSPVTRVIFHPVFSVMVSASEDATIKVWDYETGDFERTLKGHTDSVQDISFDHSGKLLASCSADMTIKLWDFQGFECIRTMHGHDHNVSSVAIMPNGDHIVSASRDKTIKMWEVQTGYCVKTFTGHREWVRMVRPNQDGTLIASCSNDQTVRVWVVATKECKAELREHEHVVECISWAPESSYSSISEATGSETKKSGKPGPFLLSGSRDKTIKMWDVSTGMCLMTLVGHDNWVRGVLFHSGGKFILSCADDKTLRVWDYKNKRCMKTLNAHEHFVTSLDFHKTAPYVVTGSVDQTVKVWECR
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
|
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Recruitment of mitotic centrosome proteins and complexes | Homo sapiens |
| Regulation of PLK1 Activity at G2/M Transition | Homo sapiens |
| Resolution of Sister Chromatid Cohesion | Homo sapiens |
| Separation of Sister Chromatids | 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:0060320 | inguinal hernia | |
| DOID:0060321 | umbilical hernia | |
| DOID:0060327 | omphalocele | |
| DOID:0060390 | distal 10q deletion syndrome | |
| DOID:0060391 | chromosome 13q14 deletion syndrome | |
| DOID:0060394 | chromosome 15q13.3 microdeletion syndrome | |
| DOID:0060395 | chromosome 15q24 deletion syndrome | |
| DOID:0060397 | chromosome 15q26-qter deletion syndrome | |
| DOID:0060398 | chromosome 16p11.2 deletion syndrome, 220-kb | |
| DOID:0060400 | chromosome 16p12.2-p11.2 deletion syndrome |
