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
External Links
Disease Ontology
DOID:0111136
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 21 - 28 of 28 in total
Gene ID Gene Symbol Description Source
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
Displaying entry 21 - 21 of 21 in total
UniProt ID Protein Name Source
Q9Y487 V-type proton ATPase 116 kDa subunit a 2
The Human Phenotype Ontology
Displaying entries 1 - 10 of 36 in total
HPO ID HPO Term
HP:0001263 Global developmental delay
HP:0008887 Adipose tissue loss
HP:0000842 Hyperinsulinemia
HP:0002155 Hypertriglyceridemia
HP:0000294 Low anterior hairline
HP:0003247 Overgrowth of external genitalia
HP:0000998 Hypertrichosis
HP:0012062 Bone cyst
HP:0001635 Congestive heart failure
HP:0000147 Polycystic ovaries
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