atrial heart septal defect 7

Summary
Synonym
  • ASD with or without atrioventricular conduction defects
  • atrial septal defect 7, with or without AV conduction defects
  • atrial septal defect-atrioventricular conduction defects syndrome
Definition
An atrial heart septal defect that has_material_basis_in heterozygous mutation in the NKX2-5 gene on chromosome 5q35.
Super Class
atrial heart septal defect autosomal dominant disease
External Links
Disease Ontology
DOID:0110112
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 38 in total
Gene ID Gene Symbol Description Source
2218 FKTN fukutin
2548 GAA alpha glucosidase
2719 GPC3 glypican 3
4594 MMUT methylmalonyl-CoA mutase
5130 PCYT1A phosphate cytidylyltransferase 1A, choline
5277 PIGA phosphatidylinositol glycan anchor biosynthesis class A
5337 PLD1 phospholipase D1
5648 MASP1 MBL associated serine protease 1
5728 PTEN phosphatase and tensin homolog
5973 RENBP renin binding protein
Related Glycoprotein
Displaying entry 31 - 31 of 31 in total
UniProt ID Protein Name Source
Q9Y625 Glypican-6

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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