abnormal rhombomere morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of any of the transiently divided segments of the developing neural tube of vertebrate embryos found within the hindbrain region in the area that will eventually become the rhombencephalon; the rhombomeres appear as a series of slightly constricted swellings in the neural tube, caudal to the cephalic flexure (Mammalian Phenotype Ontology, MP_0000933)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000933
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Genes

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

Symbol Name
CYP26A1 cytochrome P450, family 26, subfamily A, polypeptide 1
EGR2 early growth response 2
EN1 engrailed homeobox 1
FBLN1 fibulin 1
GBX2 gastrulation brain homeobox 2
GLI3 GLI family zinc finger 3
HOXA1 homeobox A1
HOXA2 homeobox A2
HOXB1 homeobox B1
HOXB2 homeobox B2
IFT172 intraflagellar transport 172
LDB1 LIM domain binding 1
LMX1A LIM homeobox transcription factor 1, alpha
LMX1B LIM homeobox transcription factor 1, beta
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
WNT1 wingless-type MMTV integration site family, member 1
ZIC2 Zic family member 2