All individuals with variants in gene PUF60

19 entries on 1 page. Showing entries 1 - 19.
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00073735 - - - F no France - - - 3y - VRJS - 1 1 Paul Kuentz
00073736 - - - M no - - - - 14y - VRJS - 1 1 Paul Kuentz
00073737 - - - M no - - - - 7y - VRJS - 1 1 Paul Kuentz
00073738 - - - M no Czech Republic - - - 17y - VRJS - 1 1 Paul Kuentz
00073739 - - - F no Belgium - - - - - VRJS - 1 1 Paul Kuentz
00078890 - - - F - - - - - - - VRJS - 1 1 Paul Kuentz
00266261 Fam6 PubMed: Charzewska 2018 3-generation family, 1 affected (M), unaffected heterozygous carrier mother M no - - - - - - ID intellectual disability, developmental delay, poor/absent speech, speech dealy/speech disturbances, hyper nasal speech, short stature, hypotonia, seizures and EEG abnormalities, corpus callosum agenesis, macrocephaly, brachycephaly, long narrow face, coarse face, prominent forehead, anteverted nares, bulbous nasal tip, small ears, open mouth, dental abnormalities, prognathism, hypertelorism, ptosis, epicentral folds, downslanted palberal fissures, sparse eyebrows, hearing loss, camptodactyly, single palmar crease, cardiac anomaly, Hirschsprung disease, constipation, anal anomaly, cryptorchidism, genital hypoplasia, hyperactive/friendly/affable 1 1 Johan den Dunnen
00296381 - - - ? - - - - - - - ? Craniosynostosis (HP:0001363); Abnormality of prenatal development or birth (HP:0001197); Intrauterine growth retardation (HP:0001511); Tetralogy of Fallot (HP:0001636); Agenesis of corpus callosum (HP:0001274) 1 1 Andreas Laner
00320170 - - - F - - - - - - - ? Thin upper lip vermilion (HP:0000219); Long philtrum (HP:0000343); Hyperopic astigmatism (HP:0000484); Delayed speech and language development (HP:0000750); Pallor (HP:0000980); Failure to thrive (HP:0001508); Short stature (HP:0004322); Abnormal fucosylation of protein N-linked glycosylation (HP:0012352); Abnormal fucosylation of O-linked protein glycosylation (HP:0012359) 1 1 IMGAG
00326212 173715 - prenatal sample - ultrasound abnormalities M ? Germany - - - - - VRJS (+) Abnormality of prenatal development or birth,(+) Increased nuchal translucency,(+) Fetal ultrasound soft marker,(+) Abnormal heart morphology 1 1 Andreas Laner
00387675 74 PubMed: Zanolli 2020 individual ID not present in paper, consecutive numbers given ? - Chile - - - - - retinal disease - 1 1 LOVD
00398755 - - - M - - - - - - - VRJS Verheij Syndrome 1 1 Michael Hildebrand
00401513 127P - - F no Spain - - - - - ID, VRJS - 1 1 Alejandro Brea-Fernández
00440406 PED3677.1 PubMed: Nambot 2018 - - - France - - - - - ? - 1 1 Johan den Dunnen
00440410 PED1525.1 PubMed: Nambot 2018 - - - France - - - - - ? - 1 1 Johan den Dunnen
00446741 281422 - - F no Germany - - - - - VRJS Neurodevelopmental delay, Delayed speech and language development, Poor fine motor coordination, Seizure, Generalized non-motor (absence) seizure, Generalized myoclonic seizure, Renal duplication, Abnormal finger phalanx morphology 1 1 Andreas Laner
00448199 Pat30 PubMed: Grimes 2023, PubMed: Poli 2024 - F - Chile - - - - - ? developmental delay; short stature; iris coloboma; chorioretinal coloboma; minor limb anomalies; pineoblastoma; dysmorphic facial features 1 1 Johan den Dunnen
00458171 - - - F - - (not applicable) white - - - - ? HP:0000104, HP:0000365, HP:0000589, HP:0000612, HP:0000750, HP:0001263, HP:0001679, HP:0002650, HP:0002721, HP:0006712, HP:0012303 1 1 Marketa Wayhelova
00460998 - - - - - Netherlands - - - - - ? - 1 1 Tjakko van Ham
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