All individuals with variants in gene CPT1A

24 entries on 1 page. Showing entries 1 - 24.
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00000010 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000024 - PubMed: Bell 2011 - - - - - - - - - BMD/DMD - 1 1 Global Variome, with Curator vacancy
00000026 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000048 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000067 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000082 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000083 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000084 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00024265 - Journal: Clemente (2014) 25 Northeast Siberian (Chukchi, Eskimo, and Koryaks) genomes with a control panel of 25 European and 11 East Asian genomes, publicly available. Complete Genomics genomes ? ? - Northeast Siberian - - - - Healthy/Control - 1 61 Marianne Vos (LOVD-team)
00181015 - - - - - - - - - - - CPTD1A - 1 1 Belen Perez
00276321 - - - F yes Turkey Turkish - - - - MPS3B, SPG54 HP:0001250 HP:0006834 HP:0031358 HP:0002240 HP:0001263 HP:0001249 HP:0000007 HP:0003676, HP:0001347 HP:0001263 HP:0001258 HP:0001249 HP:0000007 HP:0007340 HP:0003676 1 2 Dilek Gün Bilgiç
00290517 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00290518 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 105 Mohammed Faruq
00290519 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00301693 - - - M ? - - - - - - CPTD1A Cirrhosis 1 1 Ponghatai Boonsimma
00304317 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00397805 U37 PubMed: Fan 2018 - - - China - - - - - MD moderate-progressive Ullrich congenital muscular dystrophy 1 1 Johan den Dunnen
00397806 U17 PubMed: Fan 2018 - - - China - - - - - MD moderate-progressive Ullrich congenital muscular dystrophy 1 1 Johan den Dunnen
00397807 U3 PubMed: Zhang 2014, PubMed: Fan 2018 - - - China - - - - - MD mild Ullrich congenital muscular dystrophy 1 1 Johan den Dunnen
00414706 NA03575 PubMed: Bell 2011 - ? - - - - - - - retinal disease - 1 1 LOVD
00453615 Pat31 PubMed: Navarrete 2019 newborn screening - - Spain - - - - - metabolic syndrome see paper; ..., newborn screening tandem mass spectrometry dried blood spots 1 1 Johan den Dunnen
00457569 Pat12 PubMed: Kang 2018 - - - Korea - - - - - ? newborn screening; normal development 2 1 Johan den Dunnen
00457579 Pat8 PubMed: Kang 2018 - - - Korea - - - - - ? recurrent hepatic failure, nephromegaly, hemolytic anemia, rhabomyolysis, developmental delay 2 1 Johan den Dunnen
00465392 Pat63 PubMed: Chuan 2021 analysis 63 cases oculocutaneous albinism - - China - - - - - OCA1 see paper; ..., skin color white; hair color white; iris color light blue; no nystagmus 1 1 Johan den Dunnen
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