abnormal lip shape Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description changes in the characteristic contours of the fleshy margins of the mouth (Mammalian Phenotype Ontology, MP_0003771)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003771
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Genes

18 gene mutations causing the abnormal lip shape phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EDNRB endothelin receptor type B
GLI3 GLI family zinc finger 3
KIF7 kinesin family member 7
LRP6 low density lipoprotein receptor-related protein 6
MKS1 Meckel syndrome, type 1
MYH10 myosin, heavy chain 10, non-muscle
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
RAD23B RAD23 homolog B (S. cerevisiae)
RPGRIP1L RPGRIP1-like
RPL38 ribosomal protein L38
RSPO2 R-spondin 2
SATB2 SATB homeobox 2
SOX11 SRY (sex determining region Y)-box 11
TBC1D32 TBC1 domain family, member 32
TBX10 T-box 10
WDR19 WD repeat domain 19
WNT9B wingless-type MMTV integration site family, member 9B
ZEB1 zinc finger E-box binding homeobox 1