abnormal medulla oblongata morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the most caudal region of the brainstem that lies directly rostral to the spinal cord; includes regions responsible for autonomic functions such as digestion, breathing and control of heart rate (Mammalian Phenotype Ontology, MP_0000846)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000846
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Genes

23 gene mutations causing the abnormal medulla oblongata morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATRN attractin
BHLHE22 basic helix-loop-helix family, member e22
CACNA2D2 calcium channel, voltage-dependent, alpha 2/delta subunit 2
DBX1 developing brain homeobox 1
DCC DCC netrin 1 receptor
GALC galactosylceramidase
GLI3 GLI family zinc finger 3
KDM6B lysine (K)-specific demethylase 6B
KIF2A kinesin heavy chain member 2A
KIFAP3 kinesin-associated protein 3
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NTN1 netrin 1
OLIG3 oligodendrocyte transcription factor 3
PHOX2B paired-like homeobox 2b
POU4F1 POU class 4 homeobox 1
RORA RAR-related orphan receptor A
SCUBE1 signal peptide, CUB domain, EGF-like 1
UBE4B ubiquitination factor E4B
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
UNC5C unc-5 homolog C (C. elegans)
VAC14 Vac14 homolog (S. cerevisiae)
ZNF423 zinc finger protein 423