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Severe microcephaly v1.62 TRMT1 Louise Daugherty reviewed gene: TRMT1: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe microcephaly v1.62 TRMT10A Louise Daugherty reviewed gene: TRMT10A: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe microcephaly v1.61 TRMT1 Louise Daugherty Source NHS GMS was added to TRMT1.
Severe microcephaly v1.61 TRMT10A Louise Daugherty Source NHS GMS was added to TRMT10A.
Severe microcephaly v1.48 TRMT1 Rebecca Foulger gene: TRMT1 was added
gene: TRMT1 was added to Severe microcephaly. Sources: Literature
Mode of inheritance for gene: TRMT1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: TRMT1 were set to 30289604
Phenotypes for gene: TRMT1 were set to Non‐syndromal congenital microcephaly
Review for gene: TRMT1 was set to RED
Added comment: Added TRMT1 to the microcephaly panel based on PMID:30289604 (Blaesius et al., 2018) who report 4 patients from 2 unrelated consanguineous Pakistani families with homozygous variants in TRMT1 and intellectual disability. Non‐syndromal microcephaly was diagnosed at birth in three of the patients (V:2 from Family 1 (OFC -4.9 SD), and III.3 (OFC -4.1 SD) and III.4 (OFC -4 SD) from Family 2). The authors note that the clinical features are reminiscent of autosomal recessive primary microcephaly (MCPH). Rated as Red awaiting further cases.
Sources: Literature
Severe microcephaly TRMT10A Rebecca Foulger classified TRMT10A as green
Severe microcephaly TRMT10A Rebecca Foulger commented on TRMT10A
Severe microcephaly TRMT10A Rebecca Foulger commented on TRMT10A
Severe microcephaly TRMT10A Rebecca Foulger commented on TRMT10A
Severe microcephaly TRMT10A Rebecca Foulger commented on TRMT10A
Severe microcephaly TRMT10A Rebecca Foulger commented on TRMT10A