Rare genetic inflammatory skin disordersGene: NCSTN
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
ACNE INVERSA, FAMILIAL, 1; ACNINV1
Following discussion with the Genomics England clinical team it was agreed that Green genes associated with Familial hidradenitis suppurativa should be included on this panel. Therefore added to panel as a Green gene.
Created: 2 Dec 2019, 3:48 p.m. | Last Modified: 2 Dec 2019, 3:48 p.m.
Panel Version: 0.17
Phenotypes for gene: NCSTN were changed from ACNINV1; ACNE INVERSA, FAMILIAL, 1 to ACNE INVERSA, FAMILIAL, 1, OMIM:142690
Added phenotypes ACNINV1; ACNE INVERSA, FAMILIAL, 1 for gene: NCSTN Publications for gene NCSTN were changed from to 20929727
Source Expert Review Green was added to NCSTN. Rating Changed from Red List (low evidence) to Green List (high evidence)
gene: NCSTN was added gene: NCSTN was added to Rare genetic inflammatory skin disorders. Sources: Expert Review Mode of inheritance for gene: NCSTN was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown