Membrane-bound acylglycerophosphatidylinositol O-acyltransferase MBOAT7

Summary
UniProt ID
Q96N66
Gene Symbol
BB1 LENG4 MBOAT7 OACT7
Gene ID
79143
Organism
Homo sapiens (human)
GlyGen
Q96N66
PubChem
Q96N66
SwissLipids
The Human Metabolome Database
HMDBP11815
RaftProt
Q96N66
Re-Glyco
Q96N66
Annotation
Keyword
3D-structure Acyltransferase Alternative splicing Disease variant Endoplasmic reticulum Glycoprotein Intellectual disability Phospholipid biosynthesis Proteomics identification Reference proteome Transmembrane helix
Gene Ontology (GO)
GO Hierarchy
Sequence
MSPEEWTYLVVLLISIPIGFLFKKAGPGLKRWGAAAVGLGLTLFTCGPHTLHSLVTILGTWALIQAQPCSCHALALAWTFSYLLFFRALSLLGLPTPTPFTNAVQLLLTLKLVSLASEVQDLHLAQRKEMASGFSKGPTLGLLPDVPSLMETLSYSYCYVGIMTGPFFRYRTYLDWLEQPFPGAVPSLRPLLRRAWPAPLFGLLFLLSSHLFPLEAVREDAFYARPLPARLFYMIPVFFAFRMRFYVAWIAAECGCIAAGFGAYPVAAKARAGGGPTLQCPPPSSPEKAASLEYDYETIRNIDCYSTDFCVRVRDGMRYWNMTVQWWLAQYIYKSAPARSYVLRSAWTMLLSAYWHGLHPGYYLSFLTIPLCLAAEGRLESALRGRLSPGGQKAWDWVHWFLKMRAYDYMCMGFVLLSLADTLRYWASIYFCIHFLALAALGLGLALGGGSPSRRKAASQPTSLAPEKLREE
Glycosylation Sites
Displaying all 2 entries
Position Description PubMed ID GlyTouCan ID Source
98
321
  • N-linked (GlcNAc...) asparagine
Feature
  • ProtVista GlyGen : Glycosylation Site from GlyGen
  • ProtVista UniProt : Glycosylation Site from UniProt
Pathway
Displaying 1 entry
Pathway Name Organism
Acyl chain remodelling of PI Homo sapiens
Disease
Displaying 1 entry
DO ID Disease Name Source
DOID:0081219 autosomal recessive intellectual developmental disorder 57

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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026