abnormal hypothalamus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Any structural anomaly of the hypothalamus. (Human Phenotype Ontology, HP_0012286)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000837
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36 gene mutations causing the abnormal hypothalamus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
APAF1 apoptotic peptidase activating factor 1
ARNT2 aryl-hydrocarbon receptor nuclear translocator 2
AVP arginine vasopressin
BBIP1 BBSome interacting protein 1
CYCS cytochrome c, somatic
EBF2 early B-cell factor 2
ESR1 estrogen receptor 1
FGF8 fibroblast growth factor 8 (androgen-induced)
FOXB1 forkhead box B1
FYN FYN proto-oncogene, Src family tyrosine kinase
GM2A GM2 ganglioside activator
HAP1 huntingtin-associated protein 1
HESX1 HESX homeobox 1
KISS1R KISS1 receptor
NAGLU N-acetylglucosaminidase, alpha
NCOA6 nuclear receptor coactivator 6
NDN necdin, melanoma antigen (MAGE) family member
NKX2-1 NK2 homeobox 1
NR5A1 nuclear receptor subfamily 5, group A, member 1
OPN4 opsin 4
OTP orthopedia homeobox
PEG3 paternally expressed 3
POU3F2 POU class 3 homeobox 2
RAX retina and anterior neural fold homeobox
SH2D3C SH2 domain containing 3C
SHISA2 shisa family member 2
SIM1 single-minded family bHLH transcription factor 1
SOX3 SRY (sex determining region Y)-box 3
TP73 tumor protein p73
TPH2 tryptophan hydroxylase 2
TUB tubby bipartite transcription factor
UBB ubiquitin B
UCP2 uncoupling protein 2 (mitochondrial, proton carrier)
VAC14 Vac14 homolog (S. cerevisiae)
VAX1 ventral anterior homeobox 1
ZIC5 Zic family member 5