Lysophospholipid acyltransferase 7

Summary
UniProt ID
Q96N66
Gene Symbol
  • MBOAT7
  • BB1
  • LENG4
  • OACT7
Organism
Homo sapiens (human)
External Links
GlyGen
Q96N66
PubChem
Q96N66
SwissLipids
The Human Metabolome Database
HMDBP11815
The O-GlcNAc Database
Q96N66
RaftProt
Q96N66
Annotation
Keyword
  • 3D-structure
  • Acyltransferase
  • Alternative splicing
  • Disease variant
  • Endoplasmic reticulum
  • Glycoprotein
  • Intellectual disability
  • Phospholipid biosynthesis
  • Reference proteome
  • Transmembrane helix
Gene Ontology (GO)
Sequence
MSPEEWTYLVVLLISIPIGFLFKKAGPGLKRWGAAAVGLGLTLFTCGPHTLHSLVTILGTWALIQAQPCSCHALALAWTFSYLLFFRALSLLGLPTPTPFTNAVQLLLTLKLVSLASEVQDLHLAQRKEMASGFSKGPTLGLLPDVPSLMETLSYSYCYVGIMTGPFFRYRTYLDWLEQPFPGAVPSLRPLLRRAWPAPLFGLLFLLSSHLFPLEAVREDAFYARPLPARLFYMIPVFFAFRMRFYVAWIAAECGCIAAGFGAYPVAAKARAGGGPTLQCPPPSSPEKAASLEYDYETIRNIDCYSTDFCVRVRDGMRYWNMTVQWWLAQYIYKSAPARSYVLRSAWTMLLSAYWHGLHPGYYLSFLTIPLCLAAEGRLESALRGRLSPGGQKAWDWVHWFLKMRAYDYMCMGFVLLSLADTLRYWASIYFCIHFLALAALGLGLALGGGSPSRRKAASQPTSLAPEKLREE
Glycosylation Sites
Displaying all 2 entries
Position Description PubMed ID GlyTouCan ID Source
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 entries 1 - 10 of 52 in total
DO ID Disease Name Source
DOID:0060041 autism spectrum disorder
DOID:0060262 gallbladder disease
DOID:0060810 syndromic X-linked intellectual disability type 10
DOID:0060823 syndromic X-linked intellectual disability 94
DOID:10534 stomach cancer
DOID:10588 adrenoleukodystrophy
DOID:1059 intellectual disability
DOID:10907 microcephaly
DOID:10908 hydrocephalus
DOID:1094 attention deficit hyperactivity disorder

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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: August 19, 2024