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Phagocyte Defects v2.0 SENP7 Gene migrated from ENSG00000138468 to ENSG00000138468 (gene set migration)
Phagocyte Defects v1.29 SENP7 Zornitza Stark Publications for gene: SENP7 were set to PMID: 37460201; 38972567
Phagocyte Defects v1.28 SENP7 Zornitza Stark Publications for gene: SENP7 were set to PMID: 37460201
Phagocyte Defects v1.27 SENP7 Zornitza Stark Classified gene: SENP7 as Green List (high evidence)
Phagocyte Defects v1.27 SENP7 Zornitza Stark Gene: senp7 has been classified as Green List (High Evidence).
Phagocyte Defects v1.26 SENP7 Zornitza Stark reviewed gene: SENP7: Rating: GREEN; Mode of pathogenicity: None; Publications: 38972567; Phenotypes: Arthrogryposis multiplex congenita, MONDO:0015168, SENP7-related; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Phagocyte Defects v1.16 SENP7 Elena Savva Classified gene: SENP7 as Amber List (moderate evidence)
Phagocyte Defects v1.16 SENP7 Elena Savva Gene: senp7 has been classified as Amber List (Moderate Evidence).
Phagocyte Defects v1.16 SENP7 Elena Savva Classified gene: SENP7 as Amber List (moderate evidence)
Phagocyte Defects v1.16 SENP7 Elena Savva Gene: senp7 has been classified as Amber List (Moderate Evidence).
Phagocyte Defects v1.16 SENP7 Elena Savva Classified gene: SENP7 as Amber List (moderate evidence)
Phagocyte Defects v1.16 SENP7 Elena Savva Gene: senp7 has been classified as Amber List (Moderate Evidence).
Phagocyte Defects v1.15 SENP7 Elena Savva Marked gene: SENP7 as ready
Phagocyte Defects v1.15 SENP7 Elena Savva Gene: senp7 has been classified as Red List (Low Evidence).
Phagocyte Defects v1.15 SENP7 Elena Savva gene: SENP7 was added
gene: SENP7 was added to Phagocyte Defects. 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