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| Additional findings_Paediatric v1.0 | TRPM4 | Gene migrated from ENSG00000130529 to ENSG00000130529 (gene set migration) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Additional findings_Paediatric v0.2 | TRPM4 |
Zornitza Stark gene: TRPM4 was added gene: TRPM4 was added to Newborn Screening_BabySeq. Sources: Expert Review Green,BabySeq Category A gene Mode of inheritance for gene: TRPM4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: TRPM4 were set to Cardiac conduction disease |
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