autosomal dominant cutis laxa 2

Summary
Synonym
  • ADCL2
Definition
An autosomal dominant cutis laxa that has_material_basis_in heterozygous mutation in the FBLN5 gene on chromosome 14q32.
Super Class
autosomal dominant cutis laxa
External Links
Disease Ontology
DOID:0070136
Mondo Disease Ontology
OMIM
Related Genes
Displaying entries 11 - 19 of 19 in total
Gene ID Gene Symbol Description Source
9791 PTDSS1 phosphatidylserine synthase 1
11253 MAN1B1 mannosidase alpha class 1B member 1
11285 B4GALT7 beta-1,4-galactosyltransferase 7
23545 ATP6V0A2 ATPase H+ transporting V0 subunit a2
26229 B3GAT3 beta-1,3-glucuronyltransferase 3
55556 ENOSF1 enolase superfamily member 1
79644 SRD5A3 steroid 5 alpha-reductase 3
81031 SLC2A10 solute carrier family 2 member 10
126792 B3GALT6 beta-1,3-galactosyltransferase 6

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024