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Bone Marrow Failure v2.0 MDM4 Gene migrated from ENSG00000198625 to ENSG00000198625 (gene set migration)
Bone Marrow Failure v1.141 MDM4 Zornitza Stark Phenotypes for gene: MDM4 were changed from bone marrow failure syndrome MONDO:0000159, MDM4-related to bone marrow failure syndrome 6, MONDO:0030015
Bone Marrow Failure v1.140 MDM4 Zornitza Stark Classified gene: MDM4 as Green List (high evidence)
Bone Marrow Failure v1.140 MDM4 Zornitza Stark Gene: mdm4 has been classified as Green List (High Evidence).
Bone Marrow Failure v1.139 MDM4 Zornitza Stark reviewed gene: MDM4: Rating: GREEN; Mode of pathogenicity: None; Publications: 41758987; Phenotypes: bone marrow failure syndrome 6, MONDO:0030015; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Bone Marrow Failure v1.56 MDM4 Bryony Thompson Marked gene: MDM4 as ready
Bone Marrow Failure v1.56 MDM4 Bryony Thompson Gene: mdm4 has been classified as Amber List (Moderate Evidence).
Bone Marrow Failure v1.56 MDM4 Bryony Thompson Classified gene: MDM4 as Amber List (moderate evidence)
Bone Marrow Failure v1.56 MDM4 Bryony Thompson Gene: mdm4 has been classified as Amber List (Moderate Evidence).
Bone Marrow Failure v1.55 MDM4 Bryony Thompson gene: MDM4 was added
gene: MDM4 was added to Bone Marrow Failure. Sources: Other
Mode of inheritance for gene: MDM4 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: MDM4 were set to 32300648; 33104793
Phenotypes for gene: MDM4 were set to bone marrow failure syndrome MONDO:0000159, MDM4-related
Review for gene: MDM4 was set to AMBER
Added comment: A single family was reported to segregate a missense variant (p.Thr454Met) with features suggestive of dyskeratosis congenita, e.g., bone marrow hypocellularity, short telomeres, tongue squamous cell carcinoma, and acute myeloid leukemia. A mouse model of p.Thr454Met showed increased p53 activity, decreased telomere length, and bone marrow failure.
Sources: Other