abnormal ear distance/ position Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the space between or the placement of the outer ears (Mammalian Phenotype Ontology, MP_0000023)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000023
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Genes

23 gene mutations causing the abnormal ear distance/ position phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BMP5 bone morphogenetic protein 5
CHRD chordin
CISD2 CDGSH iron sulfur domain 2
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
FGFR1 fibroblast growth factor receptor 1
GLI3 GLI family zinc finger 3
HFM Hemifacial microsomia
HIC1 hypermethylated in cancer 1
HMX1 H6 family homeobox 1
HTT huntingtin
KAT6B K(lysine) acetyltransferase 6B
LMNA lamin A/C
NCOA3 nuclear receptor coactivator 3
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
PAX6 paired box 6
PRRX1 paired related homeobox 1
TBX1 T-box 1
TBX15 T-box 15
TCF15 transcription factor 15 (basic helix-loop-helix)
TCOF1 Treacher Collins-Franceschetti syndrome 1
TWIST2 twist family bHLH transcription factor 2
TWSG1 twisted gastrulation BMP signaling modulator 1
ZIC3 Zic family member 3