All individuals with variants in gene MOCS2

26 entries on 1 page. Showing entries 1 - 26.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00293883 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00302631 Pat1 PubMed: Riess 1999 - - - Egypt Coptic - - - - MOCOD - 1 1 Johan den Dunnen
00302632 Pat2 PubMed: Riess 1999 - - - Portugal - - - - - MOCOD - 1 1 Johan den Dunnen
00302633 Pat3 PubMed: Riess 1999 - - - Italy - - - - - MOCOD - 1 1 Johan den Dunnen
00302634 Pat4 PubMed: Riess 1999 - - - Germany - - - - - MOCOD - 2 1 Johan den Dunnen
00302635 Pat5 PubMed: Riess 1999 - - - France - - - - - MOCOD - 1 1 Johan den Dunnen
00302636 Pat6 PubMed: Riess 1999 - - - Portugal - - - - - MOCOD - 1 1 Johan den Dunnen
00302637 Pat7 PubMed: Riess 1999 - - - United Kingdom (Great Britain) - - - - - MOCOD - 1 1 Johan den Dunnen
00302638 patient PubMed: Johnson 2001 - F no China - - - - - MOCOD see paper; ... 2 1 Johan den Dunnen
00302639 - PubMed: Leimkuhler 2005 - - - United Kingdom (Great Britain) - - - - - MOCOD - 1 1 Johan den Dunnen
00302640 - PubMed: Leimkuhler 2005 - - - Mexico - - - - - MOCOD - 1 1 Johan den Dunnen
00302641 patient PubMed: Per 2007 2-generation family, 1 affected, 3 deceased sibs, unaffected heterozygous carrier parents/relatives M yes Turkey - - - - - MOCOD see paper; ... 1 1 Johan den Dunnen
00302642 patient PubMed: Hahnewald 2006 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Senegal - 00y00m23d - - - MOCOD see paper; ..., healthy at birth; 3d-feeding difficulties, hypotonia, drug-resistant tonic seizures and clonic seizures, elevated sulfite and diminished uric acid in urine; 21d-died cardiorespiratory arrest 1 1 Johan den Dunnen
00302643 - PubMed: Reiss 2011 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302644 - PubMed: Reiss 2011 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302645 - PubMed: Reiss 2011 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302646 - PubMed: Reiss 2011 - - - France - - - - - MOCOD - 1 1 Johan den Dunnen
00302647 - PubMed: Reiss 2003 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302648 - PubMed: Reiss 2003 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302649 - PubMed: Reiss 2003 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302650 - PubMed: Reiss 2003 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302651 - PubMed: Reiss 2003 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302652 - PubMed: Reiss 2003 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302653 - PubMed: Reiss 2003 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00302654 - PubMed: Reiss 2003 - - - - - - - - - MOCOD - 1 1 Johan den Dunnen
00428067 Pat6 PubMed: Paul 2023, Journal: Paul 2023 2-generation family, 1 affected, unaffected non carrier parents, older sister with simple febrile seizures, otherwise healthy M - United States Europe - - - - NDD brith at term; delayed speech development; delayed gross motor development; delayed fine motor milestones; mild global developmental delay; 19m-generalized-tonic clonic seizures; no autism; hypotonia; MRI brain retrocerebellar arachnoid cysts; overly friendly in comparison with two older sisters; no failure to thrive; no feeding problems; no dysmotility; no hypoventilation; no vision/eye abnormalities; no hearing impairment; no dysmorphic features; no congenital anomalies; muscle biopsy normal 1 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.