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Intellectual disability syndromic and non-syndromic v0.5216 SLC30A9 Zornitza Stark Classified gene: SLC30A9 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.5216 SLC30A9 Zornitza Stark Gene: slc30a9 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.5216 SLC30A9 Zornitza Stark Marked gene: SLC30A9 as ready
Intellectual disability syndromic and non-syndromic v0.5216 SLC30A9 Zornitza Stark Gene: slc30a9 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.5216 SLC30A9 Zornitza Stark Classified gene: SLC30A9 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.5216 SLC30A9 Zornitza Stark Gene: slc30a9 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.5216 SLC30A9 Zornitza Stark Classified gene: SLC30A9 as Green List (high evidence)
Intellectual disability syndromic and non-syndromic v0.5216 SLC30A9 Zornitza Stark Gene: slc30a9 has been classified as Green List (High Evidence).
Intellectual disability syndromic and non-syndromic v0.5215 SLC30A9 Lucy Spencer gene: SLC30A9 was added
gene: SLC30A9 was added to Intellectual disability syndromic and non-syndromic. Sources: Literature
Mode of inheritance for gene: SLC30A9 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SLC30A9 were set to 37041080
Phenotypes for gene: SLC30A9 were set to Birk-Landau-Perez syndrome (MIM#617595)
Review for gene: SLC30A9 was set to GREEN
Added comment: PMID:37041080 - 2 families previously reported and this paper describes 4 more with biallelic SLC30A9 variants. Original 2 families: 6 affected members all hom for Ala350del, and 1 affected member chet for 2 frameshifts. 4 families from this paper: 2 families have the same homozygous missense (Gly418Val), family 3 has 4 affected sibs hom for Ala350del, family 4 1 affected chet for a frameshift and a synonymous. So 2 fams homs for Ala350del and 2 fams hom for Gly418Val.
All have Brik-Landau-Perez syndrome: all with ID, movement disorder and dystonia, and many with oculomotor apraxia, renal abnormalitie, ptosis, some had hearing impairment.
Sources: Literature