NEDO human cDNA sequencing project.Wakamatsu A., Yamamoto J., Kimura K., Ishii S., Watanabe K., Sugiyama A., Murakawa K., Kaida T., Tsuchiya K.[...], Isogai T.Cited forNUCLEOTIDE SEQUENCETissueSynovial membrane tissueCategoriesSequencesSourceUniProtKB unreviewed (TrEMBL)Submission Submitted to EMBL/GenBank/DDBJ databases (JAN-2008)Cited in99+
Exome sequencing revealed DNA variants in NCOR1, IGF2BP1, SGLT2 and NEK11 as potential novel causes of ketotic hypoglycemia in children.Alhaidan Y., Larsen M.J., Schou A.J., Stenlid M.H., Al Balwi M.A., Christesen H.T., Brusgaard K.View abstractAnnotationExome sequencing revealed DNA variants in NCOR1 IGF2BP1 SGLT2 and NEK11 as potential novel causes of ketotic hypoglycemia in children.CategoriesSequencesSourceGeneRif: 79858PubMedEurope PMCSci Rep 10:2114-2114 (2020)Mapped to27
<i>NEK11</i> as a candidate high-penetrance melanoma susceptibility gene.Christodoulou E., van Doorn R., Visser M., Teunisse A., Versluis M., van der Velden P., Hayward N.K., Jochemsen A., Gruis N.View abstractAnnotationNEK11 as a candidate high-penetrance melanoma susceptibility gene.CategoriesSequencesSourceGeneRif: 79858PubMedEurope PMCJ Med Genet 57:203-210 (2020)Mapped to5