abnormal lip morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the fleshy margins of the mouth (Mammalian Phenotype Ontology, MP_0003769)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003769
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Genes

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

Symbol Name
ABCA12 ATP-binding cassette, sub-family A (ABC1), member 12
CDON cell adhesion associated, oncogene regulated
DISP1 dispatched homolog 1 (Drosophila)
EDNRB endothelin receptor type B
GLI3 GLI family zinc finger 3
HOXB1 homeobox B1
HOXB2 homeobox B2
HRAS Harvey rat sarcoma viral oncogene homolog
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
PDS5B PDS5 cohesin associated factor B
RAD23B RAD23 homolog B (S. cerevisiae)
RPGRIP1L RPGRIP1-like
RPL38 ribosomal protein L38
RSPO2 R-spondin 2
SATB2 SATB homeobox 2
SFN stratifin
SOX11 SRY (sex determining region Y)-box 11
TBC1D32 TBC1 domain family, member 32
TBX10 T-box 10
TCOF1 Treacher Collins-Franceschetti syndrome 1
TGIF1 TGFB-induced factor homeobox 1
WDR19 WD repeat domain 19
WNT9B wingless-type MMTV integration site family, member 9B
ZEB1 zinc finger E-box binding homeobox 1