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Calcium and Phosphate disorders v0.35 STX16 Zornitza Stark Mode of inheritance for gene: STX16 was changed from MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted to MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Calcium and Phosphate disorders v0.34 STX16 Zornitza Stark edited their review of gene: STX16: Changed mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, paternally imprinted (maternal allele expressed)
Calcium and Phosphate disorders v0.15 STX16 Zornitza Stark Classified gene: STX16 as Green List (high evidence)
Calcium and Phosphate disorders v0.15 STX16 Zornitza Stark Gene: stx16 has been classified as Green List (High Evidence).
Calcium and Phosphate disorders v0.14 STX16 Zornitza Stark Marked gene: STX16 as ready
Calcium and Phosphate disorders v0.14 STX16 Zornitza Stark Gene: stx16 has been classified as Green List (High Evidence).
Calcium and Phosphate disorders v0.14 STX16 Zornitza Stark Classified gene: STX16 as Green List (high evidence)
Calcium and Phosphate disorders v0.14 STX16 Zornitza Stark Gene: stx16 has been classified as Green List (High Evidence).
Calcium and Phosphate disorders v0.13 STX16 Zornitza Stark Tag SV/CNV tag was added to gene: STX16.
Calcium and Phosphate disorders v0.13 STX16 Zornitza Stark gene: STX16 was added
gene: STX16 was added to Renal abnormalities of calcium and phosphate metabolism. Sources: Expert list
Mode of inheritance for gene: STX16 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: STX16 were set to 14561710; 15579741; 27338644; 24438374
Phenotypes for gene: STX16 were set to Pseudohypoparathyroidism, type IB, MIM#603233
Review for gene: STX16 was set to GREEN
Added comment: Note multiple cases reported of recurrent 3-4kb deletion.
Sources: Expert list