abnormal thalamus morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the large ovoid mass of paired bodies containing mostly grey matter and forming part of the lateral wall of the third ventricle of the brain (Mammalian Phenotype Ontology, MP_0000832)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000832
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41 gene mutations causing the abnormal thalamus morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADCY1 adenylate cyclase 1 (brain)
AGTPBP1 ATP/GTP binding protein 1
AGTR1 angiotensin II receptor, type 1
AGTR2 angiotensin II receptor, type 2
AP3B1 adaptor-related protein complex 3, beta 1 subunit
APAF1 apoptotic peptidase activating factor 1
ARSG arylsulfatase G
ARX aristaless related homeobox
ATRN attractin
B2M beta-2-microglobulin
CD247 CD247 molecule
CD40LG CD40 ligand
CHRNB2 cholinergic receptor, nicotinic, beta 2 (neuronal)
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CYCS cytochrome c, somatic
DISC1 disrupted in schizophrenia 1
DYRK1A dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
EPHA4 EPH receptor A4
FEZF2 FEZ family zinc finger 2
FKBP8 FK506 binding protein 8, 38kDa
FOXG1 forkhead box G1
HSD17B2 hydroxysteroid (17-beta) dehydrogenase 2
HTT huntingtin
IREB2 iron-responsive element binding protein 2
MAPK8IP3 mitogen-activated protein kinase 8 interacting protein 3
MT3 metallothionein 3
MYCBP2 MYC binding protein 2, E3 ubiquitin protein ligase
NCOA6 nuclear receptor coactivator 6
NCOR1 nuclear receptor corepressor 1
NEUROG2 neurogenin 2
PAX6 paired box 6
PRNP prion protein
SOD2 superoxide dismutase 2, mitochondrial
SOX2 SRY (sex determining region Y)-box 2
TAL2 T-cell acute lymphocytic leukemia 2
TENM2 teneurin transmembrane protein 2
VAC14 Vac14 homolog (S. cerevisiae)
ZDHHC13 zinc finger, DHHC-type containing 13
ZIC3 Zic family member 3
ZIC5 Zic family member 5
ZNF423 zinc finger protein 423