All individuals with variants in gene MTOR

16 entries on 1 page. Showing entries 1 - 16.
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     
00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 3 1 Yu Sun
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 2 1 Yu Sun
00103992 Vogelaar-025A PubMed: Vogelaar 2017, Journal: Vogelaar 2017 54 patients from 53 families with genetically unexplained diffuse-type and intestinal-type gastric cancer - - - - - - - - cancer, gastric diffuse-type or intestinal-type gastric cancer 1 1 Marjolijn JL Ligtenberg
00218046 patient PubMed: Rodriguez-Garcia 2019, Journal: Rodriguez-Garcia 2019 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Spain - >13y - - - SKS, antiphospholipid syndrome, familial - 1 1 Francisco Martínez-Azorín
00226335 patient5 - - F - - - - - - - FCORD2 - 1 1 Lisa-Marie Niestroj
00234387 - - - F - - - - - - - ? - 1 1 Lisa-Marie Niestroj
00305989 Pat20 PubMed: Johannesen 2020, PubMed: Moller 2016 - F - Denmark - - - - - epilepsy - 1 1 Johan den Dunnen
00307142 Patient 06 PubMed: Mendonca 2021 - M - Brazil - - - - - RB1 Unilateral 1 1 Vanessa Mendonça
00307257 Patient 62 PubMed: Mendonca 2021 - M - Brazil - - - - - RB1 Unilateral 3 1 Vanessa Mendonça
00307260 Patient 75 PubMed: Mendonca 2021 - F - Brazil - - - - - RB1 Unilateral 1 1 Vanessa Mendonça
00325949 XI PubMed: Tjota, 2020 patient with IHC staining pattern profile of CHRCC, but molecular finding is distinct from that commonly found in CHRCC; patient's tumour correlates with low-grade oncocytic tumour (LOT) F ? (United States) - - - - - RCC - 1 1 Rosemary Ekong
00390029 16 PubMed: Ruberto 2020 - ? - Italy - - - - - retinal disease Very pale optic disk, chorioretinal atrophy in macular area, highly altered fundus 1 1 LOVD
00401645 227P - - M no Spain - - - - - ID - 1 1 Alejandro Brea-Fernández
00431130 213269 - - F no Germany - - - - - SKS Seizure, Global developmental delay, Macrocephaly, Depressed nasal bridge, Wolff-Parkinson-White syndrome 1 1 Andreas Laner
00450295 COG0020 PubMed: Tatton-Brown 2017 patient - - United States - - - - - ? overgrowth head; mild intellectual disability; 1 1 Johan den Dunnen
00450296 COG1554 PubMed: Tatton-Brown 2017 patient - - United States - - - - - ? overgrowth head; severe intellectual disability; 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.