abnormal hindbrain size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the average range of hindbrain size compared to normal (Mammalian Phenotype Ontology, MP_0012262)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012262
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Genes

9 gene mutations causing the abnormal hindbrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CSNK2A1 casein kinase 2, alpha 1 polypeptide
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
ERF Ets2 repressor factor
HIF1A hypoxia inducible factor 1, alpha subunit (basic helix-loop-helix transcription factor)
HSD17B7 hydroxysteroid (17-beta) dehydrogenase 7
ITGB1 integrin, beta 1 (fibronectin receptor, beta polypeptide, antigen CD29 includes MDF2, MSK12)
KDM2B lysine (K)-specific demethylase 2B
PAK1IP1 PAK1 interacting protein 1
ZNF423 zinc finger protein 423