congenital generalized lipodystrophy type 2

Summary
Synonym
  • Berardinelli-Seip congenital lipodystrophy type 2
  • Berardinelli-Seip syndrome
  • Brunzell syndrome BSCL2-related
  • CGL2
  • congenital lipoatrophic diabetes
  • total lipodystrophy and acromegaloid gigantism
Definition
A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of BSCL2 on chromosome 11q12.3.
Super Class
congenital generalized lipodystrophy
Disease Ontology
DOID:0111136
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
5468 PPARG peroxisome proliferator activated receptor gamma
26580 BSCL2 BSCL2 lipid droplet biogenesis associated, seipin
Displaying all 2 entries
Gene ID Gene Symbol Description Source
14705 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin
19016 Pparg peroxisome proliferator activated receptor gamma
Displaying all 2 entries
Gene ID Gene Symbol Description Source
25664 Pparg peroxisome proliferator-activated receptor gamma
361722 Bscl2 BSCL2 lipid droplet biogenesis associated, seipin
The Human Phenotype Ontology
Displaying entries 1 - 10 of 36 in total
HPO ID HPO Term
HP:0000147 Polycystic ovaries
HP:0000294 Low anterior hairline
HP:0000141 Amenorrhea
HP:0000303 Mandibular prognathia
HP:0000158 Macroglossia
HP:0001639 Hypertrophic cardiomyopathy
HP:0001015 Prominent superficial veins
HP:0003712 Skeletal muscle hypertrophy
HP:0000855 Insulin resistance
HP:0002162 Low posterior hairline
Displaying 1 entry
Gene ID Gene Symbol Description
10555 AGPAT2 1-acylglycerol-3-phosphate O-acyltransferase 2

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: December 9, 2024