abnormal rostral-caudal patterning of the somites Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the developmental pattern of the somites along the axis that runs from the rostral to the caudal region of the body (Mammalian Phenotype Ontology, MP_0008530)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0008530
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8 gene mutations causing the abnormal rostral-caudal patterning of the somites phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DLL3 delta-like 3 (Drosophila)
EFNB2 ephrin-B2
FN1 fibronectin 1
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
MESP2 mesoderm posterior basic helix-loop-helix transcription factor 2
NOG noggin
PSEN1 presenilin 1
RIPPLY2 ripply transcriptional repressor 2