dilated cardiomyopathy 1G

Summary
Synonym
  • CMD1G
Definition
A dilated cardiomyopathy that has_material_basis_in mutation in the TTN gene on chromosome 2q31.
Super Class
dilated cardiomyopathy monogenic disease
External Links
Disease Ontology
DOID:0110430
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 21 - 30 of 41 in total
Gene ID Gene Symbol Description Source
4684 NCAM1 neural cell adhesion molecule 1
4706 NDUFAB1 NADH:ubiquinone oxidoreductase subunit AB1
5130 PCYT1A phosphate cytidylyltransferase 1A, choline
5236 PGM1 phosphoglucomutase 1
5290 PIK3CA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha
5291 PIK3CB phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta
5293 PIK3CD phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit delta
5294 PIK3CG phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma
5973 RENBP renin binding protein
6389 SDHA succinate dehydrogenase complex flavoprotein subunit A
The Human Phenotype Ontology
Displaying entries 11 - 12 of 12 in total
HPO ID HPO Term
HP:0012764 Orthopnea
HP:0100578 Lipoatrophy
Displaying all 3 entries
Gene ID Gene Symbol Description
6389 SDHA succinate dehydrogenase complex flavoprotein subunit A
2218 FKTN fukutin
22845 DOLK dolichol kinase

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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