congenital generalized lipodystrophy type 1

Summary
Synonym
  • Berardinelli-Seip Congenital Lipodystrophy, Type 1
  • Brunzell syndrome AGPAT2-related
Definition
A congenital generalized lipodystrophy that has_material_basis_in an autosomal recessive mutation of AGPAT2 on chromosome 9q34.3.
Super Class
congenital generalized lipodystrophy
External Links
Disease Ontology
DOID:0111135
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 11 - 20 of 29 in total
Gene ID Gene Symbol Description Source
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5373 PMM2 phosphomannomutase 2
6319 SCD stearoyl-CoA desaturase
6389 SDHA succinate dehydrogenase complex flavoprotein subunit A
8540 AGPS alkylglycerone phosphate synthase
9663 LPIN2 lipin 2
10038 PARP2 poly(ADP-ribose) polymerase 2
The Human Phenotype Ontology
Displaying entries 51 - 60 of 60 in total
HPO ID HPO Term
HP:0001638 Cardiomyopathy
HP:0011463 Childhood onset
HP:0003577 Congenital onset
HP:0000400 Macrotia
HP:0001744 Splenomegaly
HP:0000098 Tall stature
HP:0002591 Polyphagia
HP:0000868 Decreased fertility in females
HP:0003809 Reduced intrathoracic adipose tissue
HP:0001537 Umbilical hernia
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: August 19, 2024