All individuals with variants in gene TGFBR1

48 entries on 1 page. Showing entries 1 - 48.
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00053069 - PubMed: Carmignac 2014, Journal: Carmignac 2014 2-generation family, 1 affected, unaffected non-carrier parents M no - - >06y - - - ? non-SGS Marfanoid-craniosynostosis; craniosynostosis, arachnodactyly, no pectus deformity, scoliosis, no joint contractures, no camptodactyly, foot malposition, scaphocephaly or dolichocephaly, hypertelorism, no proptosis, downslanting palpebral fissures, no micrognathia/retrognathia, no intellectual disability, hernias, no loss of subcutaneous fat, valvular anomalies, aortic root dilatation required surgery in childhood, myopia 1 1 Johan den Dunnen
00090851 - - gene panel study on colon cancer cases - - United States - - - data for MLH1, MLH3, MSH2, MSH3, MSH6, MUTYH, PMS2 in the LOVD Insight database - CRC - 1 1 Melissa DeRycke
00090852 - - gene panel study on controls - - United States - - - data for MLH1, MLH3, MSH2, MSH3, MSH6, MUTYH, PMS2 in the LOVD Insight database - Healthy/Control - 1 2 Melissa DeRycke
00090853 - - gene panel study on controls - - United States - - - data for MLH1, MLH3, MSH2, MSH3, MSH6, MUTYH, PMS2 in the LOVD Insight database - Healthy/Control - 1 1 Melissa DeRycke
00090854 - - gene panel study on colon cancer cases - - United States - - - data for MLH1, MLH3, MSH2, MSH3, MSH6, MUTYH, PMS2 in the LOVD Insight database - CRC - 1 3 Melissa DeRycke
00104008 Vogelaar-167A 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
00144417 - - 3 affecteds F - Japan Asian - - - David procedure LDS1 Pectus excavatum (HP:0000767), long fingers (HP:0100807), scoliosis (HP:0002650), high palate (HP:0000218), dural ectasia (HP:0100775), ascending aortic aneurysm (HP:0002631), carotid artery tortuosity (HP:0005302), no ectopia lentis (-HP:0001083), no hypertelorism (-HP:0000316), no bifid uvula (-HP:0000193) 1 3 Norifumi Takeda
00151836 - - - M - Japan Asian - - - - LDS1 Pectus excavatum (HP:0000767), long fingers (HP:0100807), scoliosis (HP:0002650), dural ectasia (HP:0100775), ascending aortic aneurysm (HP:0002631), hypertelorism (HP:0000316), bifid uvula (HP:0000193), Arterial tortuosity (HP:0005116), Tall stature (HP:0000098), Mitral valve prolapse (HP:0001634), no ectopia lentis (-HP:0001083) 1 1 Hironori Hara
00181216 - - - - - - - - - - - LDS1 - 1 1 Gemeinschaftspraxis für Humangenetik Dresden
00235309 - PubMed: Laterza 2019 - M no Italy - - - - - LDS1 - 1 1 Marco Ritelli
00245208 F1, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 07y - - - LDS1 - 1 1 Marco Ritelli
00245211 F2, I PubMed: Camerota 2019, Journal: Camerota 2019 - F no Italy - 31y - - - LDS1 - 1 2 Marco Ritelli
00245212 F3, I PubMed: Camerota 2019, Journal: Camerota 2019 - F no Italy - 29y - - - LDS1 - 1 1 Marco Ritelli
00245213 F4, I PubMed: Camerota 2019, Journal: Camerota 2019 patient has an affected brother carrying the same variant M no Italy - 29y - - - LDS1 - 1 2 Marco Ritelli
00245343 F5, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 47y - - - LDS1 - 1 2 Marco Ritelli
00245345 F6, I PubMed: Camerota 2019, Journal: Camerota 2019 - F no Philippines - 17y - - - LDS1 - 1 1 Marco Ritelli
00245346 F7, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 23y - - - LDS1 - 1 1 Marco Ritelli
00245347 F8, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 17y - - - LDS1 - 1 1 Marco Ritelli
00245348 F9, I PubMed: Camerota 2019, Journal: Camerota 2019 - M no Italy - 43y - - - LDS1 - 1 1 Marco Ritelli
00294693 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00295486 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00296536 - - - M - - - - - - - ? Abnormality of skeletal morphology (HP:0011842); Joint hypermobility (HP:0001382); Abnormality of central retinal artery (HP:3000032); Abnormality of ophthalmic artery (HP:0410006) 1 1 Andreas Laner
00300287 - - - F - - - - - - - ? Cleft palate (HP:0000175); Microretrognathia (HP:0000308); Muscular hypotonia (HP:0001252); Feeding difficulties (HP:0011968) 1 1 IMGAG
00303326 P41 - - M no India - - - - - LDS Aortic root dilatation (HP:0002616), Mitral valve prolapse (HP: 0001634), Scoliosis (HP:0002650) 1 2 Katta M Girisha
00373331 P1 Ritelli et al., 2021 submited - F no Italy - - - - - LDS1 - 1 2 Marco Ritelli
00373332 P3 Ritelli et al., 2021 submited - F no Italy - - - - - LDS1 - 1 1 Marco Ritelli
00398117 Pat55 PubMed: Overwater 2018 - - - Netherlands - - - - - ? see paper; ... 1 1 Johan den Dunnen
00398118 Pat56 PubMed: Overwater 2018 - - - Netherlands - - - - - ? see paper; ... 1 1 Johan den Dunnen
00398119 Pat57 PubMed: Overwater 2018 - - - Netherlands - - - - - ? see paper; ... 1 1 Johan den Dunnen
00398202 Pat147 PubMed: Overwater 2018 - - - Netherlands - - - - - ? see paper; ... 1 1 Johan den Dunnen
00398203 Pat148 PubMed: Overwater 2018 - - - Netherlands - - - - - ? see paper; ... 1 1 Johan den Dunnen
00398204 Pat149 PubMed: Overwater 2018 - - - Netherlands - - - - - ? see paper; ... 1 1 Johan den Dunnen
00418534 PatI PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418535 FamPatIIA PubMed: Almpani 2022 family, proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 2 Johan den Dunnen
00418536 FamPatIIB PubMed: Almpani 2022 offspring - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418537 FamPatIIIA PubMed: Almpani 2022 family, proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 2 Johan den Dunnen
00418538 FamPatIIIB PubMed: Almpani 2022 mother - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418539 PatIV PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418540 PatV PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418541 PatVI PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418542 FamPatVIIA PubMed: Almpani 2022 family, proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 2 Johan den Dunnen
00418543 FamPatVIIB PubMed: Almpani 2022 offspring - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418544 PatVIII PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418545 PatIX PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418546 PatX PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418547 PatXI PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00418548 PatXII PubMed: Almpani 2022 proband - - United States - - - - - LDS see paper (extensive phenotyping) 1 1 Johan den Dunnen
00462310 CONGE-021 PubMed: Boissel 2017 analysis 101 stillborn fetuses with severe prenatal anoalies - - Canada - 0d - - - ? 25gw-heart defects, posterior cleft palate with microretrognathia, clubfeet 1 1 Johan den Dunnen
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