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Date	Panel	Item	Activity
Filter activities 6 actions
28 Jul 2024	BabyScreen+ newborn screening v1.114	CLDN9	Tommy Li Added phenotypes Deafness, autosomal recessive 116 MIM#619093 for gene: CLDN9
30 Mar 2023	BabyScreen+ newborn screening v0.2146	CLDN9	Zornitza Stark Marked gene: CLDN9 as ready
30 Mar 2023	BabyScreen+ newborn screening v0.2146	CLDN9	Zornitza Stark Gene: cldn9 has been classified as Red List (Low Evidence).
30 Mar 2023	BabyScreen+ newborn screening v0.2146	CLDN9	Zornitza Stark Classified gene: CLDN9 as Red List (low evidence)
30 Mar 2023	BabyScreen+ newborn screening v0.2146	CLDN9	Zornitza Stark Gene: cldn9 has been classified as Red List (Low Evidence).
30 Mar 2023	BabyScreen+ newborn screening v0.2141	CLDN9	Lilian Downie gene: CLDN9 was added gene: CLDN9 was added to Baby Screen+ newborn screening. Sources: Expert list Mode of inheritance for gene: CLDN9 was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: CLDN9 were set to PMID: 34265170 Phenotypes for gene: CLDN9 were set to Deafness, autosomal recessive 116 MIM#619093 Review for gene: CLDN9 was set to RED Added comment: Age of onset not consistently <5 Sources: Expert list