absent eyelids Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Absent eyelids. (Human Phenotype Ontology, HP_0011224)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001341
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Genes

11 gene mutations causing the absent eyelids phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CECR2 cat eye syndrome chromosome region, candidate 2
CELSR1 cadherin, EGF LAG seven-pass G-type receptor 1
EGFR epidermal growth factor receptor
FGFR2 fibroblast growth factor receptor 2
FRAS1 Fraser extracellular matrix complex subunit 1
FREM1 FRAS1 related extracellular matrix 1
FREM2 FRAS1 related extracellular matrix protein 2
GAB1 GRB2-associated binding protein 1
SCRIB scribbled planar cell polarity protein
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
TP63 tumor protein p63