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Mitochondrial Complex V deficiency, TMEM70 type v1.2 TMEM70 Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #614052) and the OMIM record was last accessed on 20 December 2025.
Mitochondrial Complex V deficiency, TMEM70 type v1.2 TMEM70 Achchuthan Shanmugasundram Phenotypes for gene: TMEM70 were changed from to Mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, OMIM:614052; mitochondrial complex V (ATP synthase) deficiency, nuclear type 2, MONDO:0013546
Mitochondrial Complex V deficiency, TMEM70 type v1.1 Sarah Leigh Panel version 1.0 has been signed off on 2023-09-14
Mitochondrial Complex V deficiency, TMEM70 type v1.0 Sarah Leigh promoted panel to version 1.0
Mitochondrial Complex V deficiency, TMEM70 type v0.3 Sarah Leigh Panel types changed to GMS Rare Disease; GMS signed-off
Mitochondrial Complex V deficiency, TMEM70 type v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Mitochondrial Complex V deficiency, TMEM70 type v0.1 TMEM70 Achchuthan Shanmugasundram reviewed gene: TMEM70: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial Complex V deficiency, TMEM70 type v0.1 TMEM70 Achchuthan Shanmugasundram gene: TMEM70 was added
gene: TMEM70 was added to Mitochondrial Complex V deficiency, TMEM70 type. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: TMEM70 was set to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial Complex V deficiency, TMEM70 type v0.0 Achchuthan Shanmugasundram Added Panel Mitochondrial Complex V deficiency, TMEM70 type
Set list of related panels to R396
Set panel types to: GMS Rare Disease