All individuals with variants in gene ERCC6

22 entries on 1 page. Showing entries 1 - 22.
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00000010 - PubMed: Bell 2011 - - - - - - - - - - - 1 1 Global Variome, with Curator vacancy
00000057 - PubMed: Bell 2011 - - - - - - - - - - - 3 1 Global Variome, with Curator vacancy
00050608 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) F - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, autism, intrauterine growth retardation, delayed speech and language development, joint contractures of the 5th finger, seizures, microcephaly, brachycephaly, generalized hypotonia, deeply set eye, radioulnar synostosis 2 2 Johan den Dunnen
00050609 - PubMed: DDDS 2015, Journal: DDDS 2015 family, affected sibling(s) F - United Kingdom (Great Britain) - - - Decipher - ? intrauterine growth retardation, global developmental delay, autism, absent speech, seizures, microcephaly, brachycephaly, generalized hypotonia, deeply set eye 2 2 Johan den Dunnen
00081410 - Kay, submitted EJHG - - - Peru - - - - - HD - 1 1 Chris Kay
00081411 - Kay, submitted EJHG - - - Peru - - - - - HD - 1 1 Chris Kay
00081412 - Kay, submitted EJHG - - - Peru - - - - - HD - 1 1 Chris Kay
00081413 - Kay, submitted EJHG - - - Peru - - - - - HD - 1 1 Chris Kay
00248181 - PubMed: Lhota 2016 analysis 325 breast cancer cases negative for BRCA1/BRCA2/PALB2 F no Czech Republic - - - - - cancer, breast 33y ductal breast cancer, subtype luminal A 1 1 Zdenek Kleibl
00290046 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00290047 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00290048 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00290049 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 19 Mohammed Faruq
00304243 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00362007 Pat10AB PubMed: Duvvari 2016 patient - - Netherlands white - - - - retinal disease - 1 1 LOVD
00373510 RH16 PubMed: Liu 2015 - - - China - - - - - retinal disease see paper; ... 1 1 LOVD
00374312 S-4506 PubMed: Ganapathy 2019 - - - India - - - - - ? Neuroregression, nystagmus, brachydactyly and failure to thrive, suggestive of Cockayne syndrome 1 1 Johan den Dunnen
00374313 S-4707 PubMed: Ganapathy 2019 - - - India - - - - - ? Abnormal gait, spasticity, cognitive deficit, ID, microcephaly and short stature 2 1 Johan den Dunnen
00426120 10MS8500 PubMed: Al-Kasbi 2022 patient, other affecteds in family M - Oman - - - - - ID - 1 1 Johan den Dunnen
00448222 Pat124 PubMed: Poli 2024 - F - Chile - - - - - ? global developmental delay; acquired microcephaly; short stature; abnormal foot morphology 2 1 Johan den Dunnen
00453310 OCD032201 PubMed: Cappi 2016 analysis 20 sporadic obsessive-compulsive disorder cases - - Brazil - - - - - ? - 1 1 Johan den Dunnen
00459488 SYD05 IV:4 - - M yes Pakistan - - - - - CSB - 1 4 Amatul Raqeeb Jawaid
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