abnormal lacrimal gland morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the glands that secrete tears (Mammalian Phenotype Ontology, MP_0001346)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001346
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16 gene mutations causing the abnormal lacrimal gland morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCR7 chemokine (C-C motif) receptor 7
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
E2F1 E2F transcription factor 1
FGFR2 fibroblast growth factor receptor 2
FIGN fidgetin
FOXC1 forkhead box C1
ID3 inhibitor of DNA binding 3, dominant negative helix-loop-helix protein
NCDN neurochondrin
NDST1 N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1
OTX1 orthodenticle homeobox 1
PAX6 paired box 6
PITX3 paired-like homeodomain 3
PRLR prolactin receptor
SIX1 SIX homeobox 1
TP63 tumor protein p63
VSX2 visual system homeobox 2