Activity

Filter

Cancel
Date Panel Item Activity
12 actions
Renal tubulopathies v1.107 CLDN19 Eleanor Williams changed review comment from: Associated with Hypomagnesemia 5, renal, with ocular involvement 248190 in OMIM.

Many cases reported in OMIM.; to: Associated with Hypomagnesemia 5, renal, with ocular involvement 248190 in OMIM.

Many cases reported in OMIM, but note some cases have the same variant - likely founder effect.
Renal tubulopathies v1.107 CLDN19 Eleanor Williams Publications for gene: CLDN19 were set to 17033971; 22422540
Renal tubulopathies v1.106 CLDN19 Eleanor Williams Classified gene: CLDN19 as Green List (high evidence)
Renal tubulopathies v1.106 CLDN19 Eleanor Williams Added comment: Comment on list classification: Changing rating from red to green. More than 3 cases reported in OMIM.
Renal tubulopathies v1.106 CLDN19 Eleanor Williams Gene: cldn19 has been classified as Green List (High Evidence).
Renal tubulopathies v1.105 CLDN19 Eleanor Williams Added comment: Comment on publications: Publications added from OMIM
Renal tubulopathies v1.105 CLDN19 Eleanor Williams Publications for gene: CLDN19 were set to
Renal tubulopathies v1.104 CLDN19 Eleanor Williams Mode of inheritance for gene: CLDN19 was changed from to BIALLELIC, autosomal or pseudoautosomal
Renal tubulopathies v1.82 CLDN19 Eleanor Williams commented on gene: CLDN19: Associated with Hypomagnesemia 5, renal, with ocular involvement 248190 in OMIM.

Many cases reported in OMIM.
Renal tubulopathies v1.36 CLDN19 Eleanor Williams Phenotypes for gene: CLDN19 were changed from to Hypomagnesemia 5, renal, with ocular involvement, 248190
Renal tubulopathies v1.16 CLDN19 Eleanor Williams reviewed gene: CLDN19: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: Hypomagnesemia 5, renal, with ocular involvement, MIM 248190; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Renal tubulopathies v1.15 CLDN19 Eleanor Williams gene: CLDN19 was added
gene: CLDN19 was added to Renal tubulopathies. Sources: NHS GMS
Mode of inheritance for gene: CLDN19 was set to