Atypical haemolytic uraemic syndromeGene: INF2
Although associated with a clinical phenotype of aHUS it is not currently clear whether it is a primary phenomenon or secondary to FSGS
Created: 6 Aug 2019, 9:08 a.m. | Last Modified: 6 Aug 2019, 9:08 a.m.
Panel Version: 1.9
Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
FSGS MIM 613237; CHT MIM 614455
This gene was part of an initial gene list collated by Valerie Wilson, The National Renal Complement Therapeutics Centre, February 2019 on behalf of Yorkshire and North East GLH for the GMS Renal Specialist Test Group; Gene Symbol submitted: INF2; Suggested initial gene rating: none provided;
Created: 12 Feb 2019, 12:40 p.m.
Phenotypes for gene: INF2 were changed from to Charcot-Marie-Tooth disease, dominant intermediate E, 614455; Glomerulosclerosis, focal segmental, 5, 613237
Publications for gene: INF2 were set to
Mode of inheritance for gene: INF2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
gene: INF2 was added gene: INF2 was added to Atypical haemolytic uraemic syndrome. Sources: NHS GMS Mode of inheritance for gene: INF2 was set to