abnormal chemoreceptor morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of any of the cells specialized to detect chemical substances and relay that information centrally in the nervous system (Mammalian Phenotype Ontology, MP_0001001)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0001001
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Genes

26 gene mutations causing the abnormal chemoreceptor morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ASCL1 achaete-scute family bHLH transcription factor 1
ATF5 activating transcription factor 5
B3GNT2 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 2
BBS1 Bardet-Biedl syndrome 1
BBS4 Bardet-Biedl syndrome 4
CCKAR cholecystokinin A receptor
CHL1 cell adhesion molecule L1-like
CNGA2 cyclic nucleotide gated channel alpha 2
EBF2 early B-cell factor 2
EGLN3 egl-9 family hypoxia-inducible factor 3
FEZF1 FEZ family zinc finger 1
FST follistatin
GDF11 growth differentiation factor 11
GNG2 guanine nucleotide binding protein (G protein), gamma 2
GSX2 GS homeobox 2
HIST1H2BJ histone cluster 1, H2bj
KIRREL3 kin of IRRE like 3 (Drosophila)
LGALS1 lectin, galactoside-binding, soluble, 1
NPC1 Niemann-Pick disease, type C1
NPY1R neuropeptide Y receptor Y1
NPY2R neuropeptide Y receptor Y2
NXNL2 nucleoredoxin-like 2
OR8A1 olfactory receptor, family 8, subfamily A, member 1
PHOX2B paired-like homeobox 2b
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
ZEB1 zinc finger E-box binding homeobox 1