abnormality of the superior cerebellar peduncle Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An anomaly of the superior cerebellar peduncle. (Human Phenotype Ontology, HP_0011932)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011932
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7 genes associated with the abnormality of the superior cerebellar peduncle phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AHI1 Abelson helper integration site 1
CEP290 centrosomal protein 290kDa
CSPP1 centrosome and spindle pole associated protein 1
INPP5E inositol polyphosphate-5-phosphatase, 72 kDa
NPHP1 nephronophthisis 1 (juvenile)
TMEM216 transmembrane protein 216
TMEM67 transmembrane protein 67