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Arthrogryposis v0.416 SENP7 Bryony Thompson Publications for gene: SENP7 were set to PMID: 37460201
Arthrogryposis v0.415 SENP7 Bryony Thompson Classified gene: SENP7 as Green List (high evidence)
Arthrogryposis v0.415 SENP7 Bryony Thompson Gene: senp7 has been classified as Green List (High Evidence).
Arthrogryposis v0.414 SENP7 Bryony Thompson reviewed gene: SENP7: Rating: GREEN; Mode of pathogenicity: None; Publications: 37460201, 39763084, 38972567; Phenotypes: Arthrogryposis multiplex congenita, MONDO:0015168, SENP7-related; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal; Current diagnostic: yes
Arthrogryposis v0.401 SENP7 Elena Savva Classified gene: SENP7 as Amber List (moderate evidence)
Arthrogryposis v0.401 SENP7 Elena Savva Gene: senp7 has been classified as Amber List (Moderate Evidence).
Arthrogryposis v0.400 SENP7 Elena Savva Marked gene: SENP7 as ready
Arthrogryposis v0.400 SENP7 Elena Savva Gene: senp7 has been classified as Amber List (Moderate Evidence).
Arthrogryposis v0.400 SENP7 Elena Savva Classified gene: SENP7 as Amber List (moderate evidence)
Arthrogryposis v0.400 SENP7 Elena Savva Gene: senp7 has been classified as Amber List (Moderate Evidence).
Arthrogryposis v0.399 SENP7 Elena Savva gene: SENP7 was added
gene: SENP7 was added to Arthrogryposis. Sources: Literature
Mode of inheritance for gene: SENP7 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: SENP7 were set to PMID: 37460201
Phenotypes for gene: SENP7 were set to Arthrogryposis multiplex congenita, MONDO:0015168, SENP7-related
Review for gene: SENP7 was set to AMBER
Added comment: PMID: 37460201
- 1 family (4 affecteds, sibling pair and 1st cousin) with fatal arthrogryposis multiplex congenita, early respiratory failure and neutropenia. Fetus could not be tested, so 3 confirmed genetically.
- Homozygous for a PTC, decreased mRNA from one sample supports an NMD outcome.
- Additional studies performed supporting downstream proteins expression being affected
- Neutropenia observed in 2/3 patients
Sources: Literature