abnormal somite size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description atypical size of any of mesodermal clusters that are arranged segmentally along the anterior posterior axis of an embryo (Mammalian Phenotype Ontology, MP_0005222)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005222
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33 gene mutations causing the abnormal somite size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIFM1 apoptosis-inducing factor, mitochondrion-associated, 1
ALDH1A2 aldehyde dehydrogenase 1 family, member A2
APH1A APH1A gamma secretase subunit
DLL3 delta-like 3 (Drosophila)
FGFR1 fibroblast growth factor receptor 1
FOXA2 forkhead box A2
FOXO1 forkhead box O1
FURIN furin (paired basic amino acid cleaving enzyme)
HAND2 heart and neural crest derivatives expressed 2
HES7 hes family bHLH transcription factor 7
HIRA histone cell cycle regulator
HUWE1 HECT, UBA and WWE domain containing 1, E3 ubiquitin protein ligase
LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
LRP6 low density lipoprotein receptor-related protein 6
MED12 mediator complex subunit 12
MESP1 mesoderm posterior basic helix-loop-helix transcription factor 1
MSGN1 mesogenin 1
NCKAP1 NCK-associated protein 1
NOG noggin
NOTCH1 notch 1
OPA1 optic atrophy 1 (autosomal dominant)
POFUT1 protein O-fucosyltransferase 1
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
RDH10 retinol dehydrogenase 10 (all-trans)
RERE arginine-glutamic acid dipeptide (RE) repeats
ROR2 receptor tyrosine kinase-like orphan receptor 2
SHH sonic hedgehog
SSBP3 single stranded DNA binding protein 3
STK11 serine/threonine kinase 11
VANGL2 VANGL planar cell polarity protein 2
VCL vinculin
WNT5A wingless-type MMTV integration site family, member 5A
ZEB2 zinc finger E-box binding homeobox 2