small stomach Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description reduced size of the stomach (Mammalian Phenotype Ontology, MP_0002691)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002691
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Genes

17 gene mutations causing the small stomach phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCKBR cholecystokinin B receptor
CHUK conserved helix-loop-helix ubiquitous kinase
DHRS7B dehydrogenase/reductase (SDR family) member 7B
ERCC5 excision repair cross-complementation group 5
FGF10 fibroblast growth factor 10
FGFR2 fibroblast growth factor receptor 2
HES1 hes family bHLH transcription factor 1
KEAP1 kelch-like ECH-associated protein 1
LAMA3 laminin, alpha 3
NEUROG3 neurogenin 3
NFKB2 nuclear factor of kappa light polypeptide gene enhancer in B-cells 2 (p49/p100)
PBX1 pre-B-cell leukemia homeobox 1
RDH10 retinol dehydrogenase 10 (all-trans)
SHH sonic hedgehog
SOX11 SRY (sex determining region Y)-box 11
TES testin LIM domain protein
TNS3 tensin 3