All individuals with variants in gene KIF22

14 entries on 1 page. Showing entries 1 - 14.
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00050370 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected mother/child M - United Kingdom (Great Britain) - - - Decipher - ? cleft palate, micrognathia, upslanted palpebral fissure, obesity, global developmental delay 1 2 Johan den Dunnen
00050653 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, specific learning disability, constipation, hypoplasia of dental enamel 1 1 Johan den Dunnen
00050683 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) M - United Kingdom (Great Britain) - - - Decipher - ? microcephaly, abnormality of the outer ear, prominent metopic ridge, narrow mouth, inferior vermis hypoplasia, delayed speech and language development 1 2 Johan den Dunnen
00081741 Pat26 PubMed: Silveira 2021, Journal: Silveira 2021 - M no Brazil - - - - - SEMDJL2 - 1 1 Cynthia Silveira
00107945 - PubMed: Min 2011 - F - Korea - - - - - SEMDJL2 Spondyloepimetaphyseal dysplasia with joint laxity, type 2 1 1 Johan den Dunnen
00107946 - PubMed: Min 2011 - F - Korea - - - - - SEMDJL2 Spondyloepimetaphyseal dysplasia with joint laxity, type 2 1 1 Johan den Dunnen
00107947 - PubMed: Min 2011 - M - Korea - - - - - SEMDJL2 Spondyloepimetaphyseal dysplasia with joint laxity, type 2 1 1 Johan den Dunnen
00107948 - PubMed: Min 2011 - F - Korea - - - - - SEMDJL2 Spondyloepimetaphyseal dysplasia with joint laxity, type 2 2 1 Johan den Dunnen
00107949 - PubMed: Min 2011 - F - Korea - - - - - SEMDJL2 Spondyloepimetaphyseal dysplasia with joint laxity, type 2 1 1 Johan den Dunnen
00107950 - PubMed: Min 2011 - M - Korea - - - - - SEMDJL2 Spondyloepimetaphyseal dysplasia with joint laxity, type 2 1 1 Johan den Dunnen
00107951 - PubMed: Min 2011 - F - Korea - - - - - SEMDJL2 Spondyloepimetaphyseal dysplasia with joint laxity, type 2 2 1 Johan den Dunnen
00390025 3 PubMed: Ruberto 2020 - ? - Italy - - - - - retinal disease Pale and tilted optic disk associated to hypoplasia, tortuous retinal vessels, non-homogeneous macula 1 1 LOVD
00419620 8113 PubMed: Marinakis 2021 - M - Greece - - - - - ? - 1 1 Jan Traeger-Synodinos
00465860 Pat17 PubMed: Ranza 2017 patient, no family history - yes Algeria - - - - - ? see paper; ..., no intrauterine growth retadation; 3y-short stature (-3 SD); retarded bone age; joint dislocations hips; hands slender phalanges; kyphoscoliosis, hemivertebrae, sacrum anomaly, prominent heels, slender distal femur, sternal protrusion; tracheomalacia; flat nose, midface retrusion, thick lips; no intellectual disability 1 1 Johan den Dunnen
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