holoprosencephaly 1

Summary
Synonym
  • HPE1
Definition
A holoprosencephaly that has_material_basis_in variation in the chromosome region 21q22.3.
Super Class
autosomal dominant disease holoprosencephaly
External Links
Disease Ontology
DOID:0110881
Mondo Disease Ontology
OMIM
Related Genes
Displaying entries 11 - 18 of 18 in total
Gene ID Gene Symbol Description Source
10585 POMT1 protein O-mannosyltransferase 1
23556 PIGN phosphatidylinositol glycan anchor biosynthesis class N
29925 GMPPB GDP-mannose pyrophosphorylase B
29954 POMT2 protein O-mannosyltransferase 2
55624 POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
79147 FKRP fukutin related protein
80055 PGAP1 post-GPI attachment to proteins inositol deacylase 1
148789 B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 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