All individuals with variants in gene TRAPPC9

19 entries on 1 page. Showing entries 1 - 19.
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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) 1 1 Yu Sun
00050367 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) M - United Kingdom (Great Britain) - - - Decipher - ? apneic episodes in infancy, tachypnea episodic, muscular hypotonia, recurrent viral infections, motor delay, strabismus, constipation 2 2 Johan den Dunnen
00080804 - PubMed: Trujillano 2017 unaffected heterozygous carrier mother - - - - - - - - MRT13 Mental retardation, autosomal recessive 13 (OMIM:613192) 2 1 Daniel Trujillano
00105899 TRAPPC9-Patient1 Mortreux et al., submitted 2-generation family, 3 affected (1M, 2F), unaffected heterozygous carrier parents F yes Tunisia Arab >30y - Yes Supportive MRT13 Intellectual disability (HP:0001249); truncal obesity (HP:0001956); no neutropenia (HP:0001875) 1 3 Dominique Germain
00294575 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00294576 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00294577 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00294578 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 7 Mohammed Faruq
00294579 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00294580 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 24 Mohammed Faruq
00307979 17DG0781 PubMed: Anazi 2017 simplex case M - - - - - - - ID see paper; ..., Intellectual disability, Broad-based gait, Microcephaly, Periventricular leukomalacia, Bilateral coxa valga, Skeletal dysplasia 1 1 Johan den Dunnen
00361639 12DG2139 PubMed: Anazi 2017 simplex case M yes Saudi Arabia - - - - - ID syndromic; intellectual disability, progressive microcephaly, dysmorphism, hand flapping motions 1 1 Johan den Dunnen
00387752 M294 PubMed: Hu 2019 family, 2 affected individuals, first cousin parents - yes - Arab - - - - ID syndromic intellectual disability, microcephaly 1 2 Johan den Dunnen
00412313 200577 - - F yes Syria - - - - - MRT13 Microcephaly, Cerebellar vermis hypoplasia, Partial agenesis of the corpus callosum, Short stature, Pain insensitivity, Neurodevelopmental delay, Posterior atrophy of corpus callosum, Self-injurious behavior 1 1 Andreas Laner
00414555 Pat2 PubMed: Uctepe 2023 2-generation family, 1 affected, unaffected heterozygous carrier parents F yes Turkey - - - - - MRT see paper; ..., intellectual disability, autistic features 1 1 Eyyup Uctepe
00433359 FamPatII1/3;Pat28 PubMed: Duerinckx 2018, PubMed: Duerinckx 2021 2-generation family, affected sister/brother F yes Morocco - - - - - microcephaly primary microcephaly, hyperkinesia; OFC (SD-4), weigth (SD-1), length (SD-2); 8y-generalized, tonic‐clonic, treatment VPA; severe intellectual disability, no speech; MRI atrophy of the corpus callosum and cerebellum, abnormal signals in the supratentorial white matter; OFC (SD-4), weigth (SD-1), length (SD-2); 8y-generalized, tonic‐clonic, treatment VPA; severe intellectual disability, no speech; MRI atrophy of the corpus callosum and cerebellum, abnormal signals in the supratentorial white matter 1 3 Johan den Dunnen
00433370 FamPatII2 PubMed: Duerinckx 2018 unaffected sister F yes Morocco - - - - - Healthy/Control - 1 1 Johan den Dunnen
00440435 PED2274.1 PubMed: Nambot 2018 - - - France - - - - - ? - 1 1 Johan den Dunnen
00460329 Pat1 PubMed: Uctepe 2023 4-generation family, 1 affected, unaffected heterozygous carrier parents M yes Turkey - - - - - ID see paper; ..., 3.9y-microcephali, intellectual disability, motor retardation; round face, full cheeks, thin upper lip, ptosis; spasticity left ankle 2 1 Eyyup Uctepe
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