increased cranium width Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description having an increased side-to-side, or lateral distance of the cranium (Mammalian Phenotype Ontology, MP_0000441)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000441
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Genes

10 gene mutations causing the increased cranium width phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AMER1 APC membrane recruitment protein 1
ANKRD11 ankyrin repeat domain 11
ARSB arylsulfatase B
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
FGFR3 fibroblast growth factor receptor 3
LAMA2 laminin, alpha 2
PLCB1 phospholipase C, beta 1 (phosphoinositide-specific)
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
ROR2 receptor tyrosine kinase-like orphan receptor 2
RPL38 ribosomal protein L38