abnormal tongue morphology Gene Set

Dataset	MGI Mouse Phenotype Associations 2023
Category	disease or phenotype associations
Type	phenotype
Description	any structural anomaly of the mobile mass of muscular tissue and surrounding epithelial tissue occupying the cavity of the mouth and forming part of the floor (Mammalian Phenotype Ontology, MP_0000762)
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Genes

28 gene mutations causing the abnormal tongue morphology phenotype in transgenic mice from the MGI Mouse Phenotype Associations 2023 dataset.

Symbol	Name
CACNA1S	calcium channel, voltage-dependent, L type, alpha 1S subunit
COL7A1	collagen, type VII, alpha 1
CPLANE1	ciliogenesis and planar polarity effector complex subunit 1
CTNNB1	catenin (cadherin-associated protein), beta 1, 88kDa
DSG3	desmoglein 3
EDN1	endothelin 1
EGFR	epidermal growth factor receptor
FGF10	fibroblast growth factor 10
FGFR2	fibroblast growth factor receptor 2
FUZ	fuzzy planar cell polarity protein
GALNT3	polypeptide N-acetylgalactosaminyltransferase 3
ICK	intestinal cell (MAK-like) kinase
IFT27	intraflagellar transport 27
IMPA1	inositol(myo)-1(or 4)-monophosphatase 1
KRT13	keratin 13, type I
KRT4	keratin 4, type II
LARGE	like-glycosyltransferase
LGR5	leucine-rich repeat containing G protein-coupled receptor 5
LMNA	lamin A/C
MET	MET proto-oncogene, receptor tyrosine kinase
NF1	neurofibromin 1
PRDM16	PR domain containing 16
SALL3	spalt-like transcription factor 3
SFN	stratifin
SOX2	SRY (sex determining region Y)-box 2
TMEM107	transmembrane protein 107
TP53	tumor protein p53
WNT10A	wingless-type MMTV integration site family, member 10A