abnormal eyelid development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description aberrant formation of the skin folds covering the front of the eyeball (Mammalian Phenotype Ontology, MP_0009651)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009651
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23 gene mutations causing the abnormal eyelid development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADAM17 ADAM metallopeptidase domain 17
ALX3 ALX homeobox 3
APAF1 apoptotic peptidase activating factor 1
DSC1 desmocollin 1
EGFR epidermal growth factor receptor
IGF2 insulin-like growth factor 2
IKZF2 IKAROS family zinc finger 2 (Helios)
JUN jun proto-oncogene
LIMK2 LIM domain kinase 2
LRP6 low density lipoprotein receptor-related protein 6
LUZP1 leucine zipper protein 1
MAP3K1 mitogen-activated protein kinase kinase kinase 1, E3 ubiquitin protein ligase
NFIB nuclear factor I/B
OSR2 odd-skipped related transciption factor 2
PAX6 paired box 6
PPP1R13L protein phosphatase 1, regulatory subunit 13 like
PVRL1 poliovirus receptor-related 1 (herpesvirus entry mediator C)
SEC24B SEC24 family member B
SFN stratifin
TBX10 T-box 10
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)
TGFA transforming growth factor, alpha
VANGL2 VANGL planar cell polarity protein 2