abnormal midgut morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the portion of the embryonic gut between the foregut and the hindgut, which originally is open to the yolk sac (Mammalian Phenotype Ontology, MP_0009705)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009705
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6 gene mutations causing the abnormal midgut morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FOXF1 forkhead box F1
FURIN furin (paired basic amino acid cleaving enzyme)
RDH10 retinol dehydrogenase 10 (all-trans)
RUNX1T1 runt-related transcription factor 1; translocated to, 1 (cyclin D-related)
SOX17 SRY (sex determining region Y)-box 17
WNT5A wingless-type MMTV integration site family, member 5A