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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
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9UGN5 | Poly [ADP-ribose] polymerase 2 | |
| Q9Y487 | V-type proton ATPase 116 kDa subunit a 2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000819 | Diabetes mellitus |
| HP:0001999 | Abnormal facial shape |
| HP:0000158 | Macroglossia |
| HP:0001508 | Failure to thrive |
| HP:0003124 | Hypercholesterolemia |
| HP:0000956 | Acanthosis nigricans |
| HP:0003623 | Neonatal onset |
| HP:0000787 | Nephrolithiasis |
| HP:0002833 | Cystic angiomatosis of bone |
| HP:0000877 | Insulin-resistant diabetes mellitus at puberty |
