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- NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_assertion type Assertion NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_head.
- NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_assertion description "[In humans, a mutation in the Glis2 gene has been linked to the development of nephronophthisis (NPHP), a recessive cystic kidney disease, while mutations in Glis3 lead to an extended multisystem phenotype that includes the development of neonatal diabetes, polycystic kidneys, congenital hypothyroidism, and facial dysmorphism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_provenance.
- NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_assertion evidence source_evidence_literature NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_provenance.
- NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_assertion SIO_000772 22391303 NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_provenance.
- NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_assertion wasDerivedFrom befree-2016 NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_provenance.
- NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_assertion wasGeneratedBy ECO_0000203 NP965530.RADK15-10GMfHavZuzw1PhIhFo_vkWf0qRKXc1Hug83yA130_provenance.