BSCL2 lipid droplet biogenesis associated, seipin

Summary
Gene Symbol
  • BSCL2
Organism
Homo sapiens (human)
NCBI Gene
26580
PubChem
26580
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Congenital generalized lipodystrophy
  • Diabetes mellitus
  • Disease variant
  • Endoplasmic reticulum
  • Glycoprotein
  • Hereditary spastic paraplegia
  • Lipid degradation
  • Lipid droplet
  • Lipid metabolism
  • Neuropathy
  • Phosphoprotein
  • Reference proteome
  • Transmembrane helix
Proteins
Displaying all 2 entries
UniProt Protein Name
A0A024R549
Q96G97
  • Bernardinelli-Seip congenital lipodystrophy type 2 protein
Gene Ontology (GO)
GO Hierarchy
OrthoDB (Group)
Group level
Eukaryota
Group Name
Seipin
Functional Category
  • E: Amino acid transport and metabolism
  • Q: Secondary metabolites biosynthesis, transport and catabolism
  • T: Signal transduction mechanisms
Displaying 1 entry
InterPro
Seipin family
Disease
Disease Ontology
Displaying all 5 entries
DO ID Disease Name Source
DOID:0081401 autosomal dominant distal hereditary motor neuronopathy 13
DOID:0110770 hereditary spastic paraplegia 17
DOID:0111136 congenital generalized lipodystrophy type 2
DOID:2476 hereditary spastic paraplegia
DOID:811 lipodystrophy

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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: March 31, 2025