head tilt Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description condition in which the portion of the body containing the brain and organs of sight, hearing, taste, and smell lists to the side (Mammalian Phenotype Ontology, MP_0005191)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005191
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Genes

34 gene mutations causing the head tilt phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AP3D1 adaptor-related protein complex 3, delta 1 subunit
ATG4B autophagy related 4B, cysteine peptidase
ATP6V0A4 ATPase, H+ transporting, lysosomal V0 subunit a4
BDNF brain-derived neurotrophic factor
BLOC1S4 biogenesis of lysosomal organelles complex-1, subunit 4, cappuccino
BLOC1S5 biogenesis of lysosomal organelles complex-1, subunit 5, muted
BLOC1S6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
CDH23 cadherin-related 23
CYBA cytochrome b-245, alpha polypeptide
FGF3 fibroblast growth factor 3
FOXI1 forkhead box I1
GFI1 growth factor independent 1 transcription repressor
GRID2 glutamate receptor, ionotropic, delta 2
HMX2 H6 family homeobox 2
LHFPL5 lipoma HMGIC fusion partner-like 5
LOC102723475 putative uncharacterized protein LOC388820
MYO15A myosin XVA
MYO6 myosin VI
MYO7A myosin VIIA
NDUFS4 NADH dehydrogenase (ubiquinone) Fe-S protein 4, 18kDa (NADH-coenzyme Q reductase)
NEUROD1 neuronal differentiation 1
NOX3 NADPH oxidase 3
NOXO1 NADPH oxidase organizer 1
OTOG otogelin
OTOP1 otopetrin 1
PCDH15 protocadherin-related 15
S1PR2 sphingosine-1-phosphate receptor 2
SELE selectin E
SELP selectin P (granule membrane protein 140kDa, antigen CD62)
SLC12A2 solute carrier family 12 (sodium/potassium/chloride transporter), member 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
TBX1 T-box 1
TBX10 T-box 10
TMIE transmembrane inner ear