Disease: Familial Progressive Cardiac Conduction Defect

Familial Progressive Cardiac Conduction Defect
cardiac, genetic
Associated Genes
SCN5A (Withdrawn symbols: CDCD2, CMD1E, CMPD2, HB1, HB2, HBBD, HH1, ICCD, IVF, LQT3, Nav1.5, PFHB1, SSS1 ) , NKX2-5 (Withdrawn symbols: CSX, CSX1, NKX2.5, NKX2E, NKX4-1 ) , TRPM4 (Withdrawn symbols: FLJ20041 ) , SCN1B
Mouse Orthologs
Scn5a , Nkx2-5 (Withdrawn symbols: Csx ) , Trpm4 (Withdrawn symbols: 1110030C19Rik, AW047689 ) , Scn1b
ORPHA:871 (names, synonyms, disease associated genes),
Orphanet (disease classes),
HGNC, Ensembl, MGI (gene symbols, gene orthology)
HPO (phenotypes)

Mouse Models

Learn about how to interpret our results in the Disease Models Help pages

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