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DDG2P v3.12 ESCO2 Achchuthan Shanmugasundram reviewed gene: ESCO2: Rating: GREEN; Mode of pathogenicity: ; Publications: 3740099, 15821733, 495649; Phenotypes: ROBERTS SYNDROME, OMIM:268300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
DDG2P v3.11 ESCO2 Achchuthan Shanmugasundram Publications for gene: ESCO2 were updated from 15821733; 495649 to 3740099; 15821733; 495649
DDG2P v0.2 ESCO2 Rebecca Foulger reviewed gene: ESCO2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
DDG2P v0.1 ESCO2 Rebecca Foulger Added phenotypes ROBERTS SYNDROME 268300 for gene: ESCO2
Publications for gene ESCO2 were changed from 3740099 to 15821733; 495649
DDG2P v0.1 ESCO2 Rebecca Foulger gene: ESCO2 was added
gene: ESCO2 was added to DDG2P. Sources: Expert Review Green,DD-Gene2Phenotype
Mode of inheritance for gene: ESCO2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ESCO2 were set to 3740099
Phenotypes for gene: ESCO2 were set to SC PHOCOMELIA SYNDROME 269000