abnormal optic stalk morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the narrow, proximal portion of the optic vesicle which connects the embryonic eye and forebrain (Mammalian Phenotype Ontology, MP_0004268)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004268
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11 gene mutations causing the abnormal optic stalk morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CASP3 caspase 3, apoptosis-related cysteine peptidase
CSNK2A1 casein kinase 2, alpha 1 polypeptide
GLI3 GLI family zinc finger 3
HHEX hematopoietically expressed homeobox
MITF microphthalmia-associated transcription factor
NR2E1 nuclear receptor subfamily 2, group E, member 1
PAX2 paired box 2
SHH sonic hedgehog
SLC12A6 solute carrier family 12 (potassium/chloride transporter), member 6
TFAP2A transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)
VSX2 visual system homeobox 2