All individuals with variants in gene KAL1

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) 4 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) 5 1 Yu Sun
00037751 19377180-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 1 Lucy Raymond
00037752 19377181-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 92 Lucy Raymond
00037753 19377182-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 1 Lucy Raymond
00037754 19377183-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 100 Lucy Raymond
00037755 - - - M no (China) Han Chinese - - - - HH1;KAL1 hypogonadotropic hypogonadism, anosmia or hyposmia, no mental retardation 1 1 Fei Wang
00037756 - - - F no (United Kingdom (Great Britain)) - - - - - dysplasia, septo-optic ectopic posterior pituitary and bilateral optic nerve hypoplasia. ACTH, TSH and GH deficiency. Poor response to GnRH, puberty induced. 1 1 Mark McCabe
00037757 - - - M - Belgium European - - - - HH1;KAL1 hypogonatropic hypogonadism, anosmy, cryptorchidism 1 1 Cecile Libioulle
00037758 - - variant detected in two sisters F no Australia African/white - - - - dysplasia, septo-optic elder sibling had bilateral optic nerve hypoplasia, hypoplastic optic chiasm and cavum septum pellucidum; younger sibling also presented the first two characteristics, plus a thinning corpus callosum, anterior pituitary hypoplasia and an absent posterior pituitary. 1 2 Mark McCabe
00039390 - PubMed: Bosch 2016, Journal: Bosch 2016 - M no Netherlands - - - - - CVI, ID - 1 1 Danielle Bosch
00081734 - PubMed: Hanchate 2012, Journal: Hanchate 2012 targeted sequencing in 386 Kallmann syndrome patients, 1 affected M - France - - - - - KAL - 1 1 Johan den Dunnen
00104952 - - - M ? Israel Jewish - - - - ANI - 1 1 Anna Alkelai
00231456 Pat76 PubMed: Eggers 2016 - M - - - - - - - DSD disorder of sex development 1 1 Johan den Dunnen
00231472 Pat108 PubMed: Eggers 2016 - - - - - - - - - DSD disorder of sex development 1 1 Johan den Dunnen
00231501 Pat172 PubMed: Eggers 2016 - M - - - - - - - DSD disorder of sex development 1 1 Johan den Dunnen
00316110 K158 PubMed: Heidet 2017 affected fetus and 1st degree relative - - France - - - - - CAKUT bilateral kidney agenesis 1 2 Johan den Dunnen
00316145 K26 PubMed: Heidet 2017 fetus - - France - - - - - CAKUT bilateral kidney agenesis 1 1 Johan den Dunnen
00395575 RP-1018 PubMed: Perea-Romero 2021 - - - Spain - - - - - retinal disease astigmatism, early onset rod-cone dystrophy, hypermetropia, strabismus, global developmental delay, tip-toe gait, talipes equinovarus, anteverted nares, broad nasal tip, depressed nasal bridge, hypertelorism, long philtrum, low anterior hairline, narrow palate, retrognathia, thin vermilion border 1 1 LOVD
00435425 patient - - M no Poland white - - - none KAL - 1 1 Katarzyna Bilińska
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