intrinsic cardiomyopathy

Summary
Definition
A cardiomyopathy that is characterized as weakness in the muscle of the heart that is not due to an identifiable external cause.
Super Class
cardiomyopathy
Disease Ontology
DOID:0060036
MGI genotype (from TogoID)
Related Genes
Displaying all 10 entries
Gene ID Gene Symbol Description Source
908 CCT6A chaperonin containing TCP1 subunit 6A
1829 DSG2 desmoglein 2
4625 MYH7 myosin heavy chain 7
4878 NPPA natriuretic peptide A
6157 RPL27A ribosomal protein L27a
6188 RPS3 ribosomal protein S3
7203 CCT3 chaperonin containing TCP1 subunit 3
10575 CCT4 chaperonin containing TCP1 subunit 4
23002 DAAM1 dishevelled associated activator of morphogenesis 1
51650 MRPS33 mitochondrial ribosomal protein S33
Displaying all 6 entries
Gene ID Gene Symbol Description Source
12462 Cct3 chaperonin containing TCP1 subunit 3
13511 Dsg2 desmoglein 2
20103 Rps5 ribosomal protein S5
27050 Rps3 ribosomal protein S3
140781 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta
208846 Daam1 dishevelled associated activator of morphogenesis 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
24837 Tnnt2 troponin T2, cardiac type
Displaying 1 entry
Gene ID Gene Symbol Description Source
42761 RpS3 Ribosomal protein S3
Displaying 1 entry
Gene ID Gene Symbol Description Source
851412 CCT4 chaperonin-containing T-complex subunit CCT4

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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: December 9, 2024