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| DDG2P v3.21 | KCNK9 | Achchuthan Shanmugasundram Phenotypes for gene: KCNK9 were changed from BIRK-BAREL SYNDROME, OMIM:612292 to BIRK-BAREL SYNDROME, OMIM:612292 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v3.21 | KCNK9 | Achchuthan Shanmugasundram Phenotypes for gene: KCNK9 were changed from BIRK-BAREL SYNDROME, OMIM:612292 to BIRK-BAREL SYNDROME, OMIM:612292 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v3.21 | KCNK9 | Achchuthan Shanmugasundram Phenotypes for gene: KCNK9 were changed from BIRK-BAREL SYNDROME 612292 to BIRK-BAREL SYNDROME, OMIM:612292 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v3.12 | KCNK9 | Achchuthan Shanmugasundram reviewed gene: KCNK9: Rating: RED; Mode of pathogenicity: Other; Publications: ; Phenotypes: BIRK-BAREL SYNDROME, OMIM:612292; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v3.11 | KCNK9 |
Achchuthan Shanmugasundram Mode of inheritance for gene KCNK9 was changed from MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed) to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed) Mode of pathogenicity for gene KCNK9 was changed from Other - please provide details in the comments to Other |
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| DDG2P v0.2 | KCNK9 | Rebecca Foulger reviewed gene: KCNK9: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| DDG2P v0.1 | KCNK9 |
Rebecca Foulger gene: KCNK9 was added gene: KCNK9 was added to DDG2P. Sources: Expert Review Red,DD-Gene2Phenotype Mode of inheritance for gene: KCNK9 was set to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed) Phenotypes for gene: KCNK9 were set to BIRK-BAREL SYNDROME 612292 Mode of pathogenicity for gene: KCNK9 was set to Other - please provide details in the comments |
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