cerebellum hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000851
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Genes

16 gene mutations causing the cerebellum hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHI1 Abelson helper integration site 1
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
COMMD3-BMI1 COMMD3-BMI1 readthrough
CSTB cystatin B (stefin B)
CTNNA2 catenin (cadherin-associated protein), alpha 2
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
ERBB3 erb-b2 receptor tyrosine kinase 3
FZD4 frizzled class receptor 4
KIF14 kinesin family member 14
PURA purine-rich element binding protein A
RPGRIP1L RPGRIP1-like
SHH sonic hedgehog
TP53 tumor protein p53
ZIC1 Zic family member 1
ZIC4 Zic family member 4
ZNF423 zinc finger protein 423