All individuals with variants in gene STIM1

20 entries on 1 page. Showing entries 1 - 20.
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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) 2 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
00029011 - PubMed: Nesin 2014 3-generation family, 1 affected M ? United States - - - - - STRMK see paper; congenital miosis, bleeding diathesis, thrombocytopenia, proximal muscle weakness 1 1 Johan den Dunnen
00029012 - PubMed: Nesin 2014 2-generation family, 1 affected M - United States - - - - - STRMK see paper; congenital miosis, bleeding diathesis, thrombocytopenia, proximal muscle weakness 1 1 Johan den Dunnen
00234377 - - - M no France - - - - - TAM1 - 1 1 Johann Böhm
00234378 - - - F ? Italy - - - - - TAM1 - 1 1 Johann Böhm
00234379 - - - F yes Eritrea - - - - - TAM1 - 1 1 Johann Böhm
00266102 FamPatV1 PubMed: Picard 2009 5-generation family, 3 affected sibs (2F, M), unaffected heterozygous carrier parents/relatives F yes France - 9y - - - IMD infection with Escherichia coli and Streptococcus pneu-moniae resulting in sepsis, urinary tract infections, pneumonia, infection with CMV and VZV; hemolytic anemia, thrombocytopenia; lymphadenopathy, hepatosplenomegaly; muscular hypotonia, partial iris hypoplasia, abnormal dental enamel; 9y-died from hematopoietic stem-cell transplantation complications 1 3 Johan den Dunnen
00266104 FamPatV7 PubMed: Picard 2009 - M yes France - - - - - IMD undocumented sepsis, treatment with IV immune globulin since birth; thrombocytopenia; no lymphoproliferative disorder; muscular hypotonia, partial iris hypoplasia, abnormal dental enamel, hypoglycemia; 15m-hematopoietic stem-cell transplantation, currently alive and well with muscular hypotonia 1 1 Johan den Dunnen
00266105 FamPatIV2 PubMed: Byun 2010 4-generation family, 1 affected, unaffected heterozygous carrier parents/relatives F yes Turkey - 2y4m - - - IMD see paper; … 1 1 Johan den Dunnen
00266381 1.II.2 PubMed: Morin 2019 - M no France - - - - - TAM1 Axial muscle weakness, myalgia, diabetes, hypertension, lipodystrophy, coronary artery disease. Muscle biopsy: tubular aggregates, fiber size variability, type I fiber predominance, internal nuclei 1 1 Johann Böhm
00266385 - PubMed: Bohm 2014 - M yes Italy - - - - - TAM1 Lower limb weakness, myalgia, eye movement defects. Muscle biopsy: tubular aggregates, fiber size variability, internal nuclei, fibrosis 1 1 Johann Böhm
00269322 I.1 PubMed: Walter 2015 - M no Germany - - - - - TAM1 - 1 1 Johann Böhm
00271177 Fam1PatII1 PubMed: Böhm 2013 - M no - - - - - - TAM1 Upper and lower limb muscle weakness, eye movement defects, contractures 1 1 Johann Böhm
00271178 - PubMed: Noury 2017 - F no Portugal - - - - - TAM1 Lower limb muscle weakness, cramps, eye movement defects, contractures, asplenia, short stature, hypocalcemia, anemia, tooth enamel hypocalcification, 1 1 Johann Böhm
00287377 - - - F ? Belgium - 20y - - - LGMD psoas weakness, pelvic girdle weakness, tibialis anterior weakness, easy fatigability 1 1 Alicia Alonso-Jiménez
00290391 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00290392 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 8 Mohammed Faruq
00290393 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 11 Mohammed Faruq
00466395 - Pending - F - France - - - - - TAM1 Limb-girdle muscular dystrophy * Motor delay * Hyperlordosis * Muscle fiber necrosis * Increased endomysial connective tissue * Abnormal circulating creatine kinase concentration * Specific learning disability 1 1 Camille Verebi
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