abnormal lacrimal gland physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the glands that secrete tears (Mammalian Phenotype Ontology, MP_0001348)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001348
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16 gene mutations causing the abnormal lacrimal gland physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AIRE autoimmune regulator
CCR7 chemokine (C-C motif) receptor 7
CDO1 cysteine dioxygenase type 1
FAM20C family with sequence similarity 20, member C
FAS Fas cell surface death receptor
FOXC1 forkhead box C1
ID3 inhibitor of DNA binding 3, dominant negative helix-loop-helix protein
IL4 interleukin 4
MAP3K14 mitogen-activated protein kinase kinase kinase 14
MC5R melanocortin 5 receptor
NFKBIZ nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, zeta
NRTN neurturin
TGFB1 transforming growth factor, beta 1
THBS1 thrombospondin 1
TRAF3IP2 TRAF3 interacting protein 2
XCL1 chemokine (C motif) ligand 1