abnormal podocyte slit junction morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the gaps between the interdigitated foot processes of the podocyte (Mammalian Phenotype Ontology, MP_0008062)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008062
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10 gene mutations causing the abnormal podocyte slit junction morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CD151 CD151 molecule (Raph blood group)
DDR1 discoidin domain receptor tyrosine kinase 1
FAT1 FAT atypical cadherin 1
FOXC2 forkhead box C2
GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
HPRT1 hypoxanthine phosphoribosyltransferase 1
LMX1B LIM homeobox transcription factor 1, beta
NPHS1 nephrosis 1, congenital, Finnish type (nephrin)
NPHS2 nephrosis 2, idiopathic, steroid-resistant (podocin)
PODXL podocalyxin-like