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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 10554 | AGPAT1 | 1-acylglycerol-3-phosphate O-acyltransferase 1 | |
| 10555 | AGPAT2 | 1-acylglycerol-3-phosphate O-acyltransferase 2 | |
| 11285 | B4GALT7 | beta-1,4-galactosyltransferase 7 | |
| 22845 | DOLK | dolichol kinase | |
| 23175 | LPIN1 | lipin 1 | |
| 23545 | ATP6V0A2 | ATPase H+ transporting V0 subunit a2 | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 57104 | PNPLA2 | patatin like phospholipase domain containing 2 | |
| 64132 | XYLT2 | xylosyltransferase 2 |
Related Glycoprotein
- The Human Phenotype Ontology
| 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 |
