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Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Phenotypes for gene: ERBB2 were changed from Visceral neuropathy, familial, 2, autosomal recessive, MIM # 619465, Complex neurocristinopathy to Visceral neuropathy, familial, 2, autosomal recessive, MIM # 619465, Complex neurocristinopathy
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.365 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.366 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 33497358
Deafness_IsolatedAndComplex v1.365 ERBB2 Chirag Patel Publications for gene: ERBB2 were set to 40329538; 33720042
Deafness_IsolatedAndComplex v1.365 ERBB2 Chirag Patel Phenotypes for gene: ERBB2 were changed from Congenital heart disease - left ventricular outflow tract obstruction defects; MONDO:0005453; Hirschsprung disease (HSCR, aganglionic megacolon, MIM#142623) to Visceral neuropathy, familial, 2, autosomal recessive, MIM # 619465, Complex neurocristinopathy
Deafness_IsolatedAndComplex v1.365 ERBB2 Chirag Patel Mode of inheritance for gene: ERBB2 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to BIALLELIC, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v1.364 ERBB2 Chirag Patel Classified gene: ERBB2 as Red List (low evidence)
Deafness_IsolatedAndComplex v1.364 ERBB2 Chirag Patel Gene: erbb2 has been classified as Red List (Low Evidence).
Deafness_IsolatedAndComplex v1.364 ERBB2 Chirag Patel Classified gene: ERBB2 as Red List (low evidence)
Deafness_IsolatedAndComplex v1.364 ERBB2 Chirag Patel Gene: erbb2 has been classified as Red List (Low Evidence).
Deafness_IsolatedAndComplex v1.363 ERBB2 Chirag Patel Marked gene: ERBB2 as ready
Deafness_IsolatedAndComplex v1.363 ERBB2 Chirag Patel Gene: erbb2 has been classified as Amber List (Moderate Evidence).
Deafness_IsolatedAndComplex v1.363 Chirag Patel Copied gene ERBB2 from panel Mendeliome
Deafness_IsolatedAndComplex v1.363 ERBB2 Chirag Patel gene: ERBB2 was added
gene: ERBB2 was added to Deafness_IsolatedAndComplex. Sources: Expert Review Amber,Victorian Clinical Genetics Services
Mode of inheritance for gene: ERBB2 was set to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Publications for gene: ERBB2 were set to 40329538; 33720042
Phenotypes for gene: ERBB2 were set to Congenital heart disease - left ventricular outflow tract obstruction defects; MONDO:0005453; Hirschsprung disease (HSCR, aganglionic megacolon, MIM#142623)