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Severe Paediatric Disorders v0.17 AMMECR1 Louise Daugherty Mode of inheritance for gene AMMECR1 was changed from to X-LINKED: hemizygous mutation in males, biallelic mutations in females
Severe Paediatric Disorders v0.12 AMMECR1 Louise Daugherty reviewed gene: AMMECR1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 AMMECR1 Louise Daugherty Publications for gene AMMECR1 were updated from to 30847515
Severe Paediatric Disorders v0.10 AMMECR1 Louise Daugherty Added phenotypes Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, 300990 for gene: AMMECR1
Severe Paediatric Disorders v0.9 AMMECR1 Louise Daugherty Added phenotypes Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, 300990 for gene: AMMECR1
Severe Paediatric Disorders v0.9 AMMECR1 Louise Daugherty Added phenotypes Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, 300990 for gene: AMMECR1
Severe Paediatric Disorders v0.8 AMMECR1 Louise Daugherty Added phenotypes Midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, 300990 for gene: AMMECR1
Severe Paediatric Disorders v0.7 AMMECR1 Louise Daugherty Source Next Generation Children Project was added to AMMECR1.
Severe Paediatric Disorders v0.5 AMMECR1 Louise Daugherty Source Expert Review Green was added to AMMECR1.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 AMMECR1 Louise Daugherty gene: AMMECR1 was added
gene: AMMECR1 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: AMMECR1 was set to