Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		1.000 Biomarker CLINGEN These results demonstrate the advantages of using de novo Zeb2 Δex7/+ mice with the C57BL/6 background as the MOWS model. 26319231

2015
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		1.000 Biomarker CLINGEN Zfhx1b induces a definitive neural stem cell fate in mouse embryonic stem cells. 22594450

2012
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		1.000 Biomarker CLINGEN Neural crest-specific removal of Zfhx1b in mouse leads to a wide range of neurocristopathies reminiscent of Mowat-Wilson syndrome. 17478475

2007
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		1.000 Biomarker CLINGEN A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype. 16688751

2006
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		1.000 Biomarker CLINGEN Mowat-Wilson Syndrome is a recently delineated mental retardation syndrome usually associated with multiple malformations and a recognizable facial phenotype caused by defects of the transcriptional repressor ZFHX1B. 16053902

2005
Entrez Id: 9839
Gene Symbol: ZEB2
ZEB2
CUI: C1856113
Disease: Mowat-Wilson syndrome
Mowat-Wilson syndrome 		1.000 Biomarker CLINGEN Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23. 9719364

1998