abnormal forebrain size Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the average range of forebrain size compared to normal (Mammalian Phenotype Ontology, MP_0012137)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0012137
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Genes

37 gene mutations causing the abnormal forebrain size phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AKAP13 A kinase (PRKA) anchor protein 13
ARID1A AT rich interactive domain 1A (SWI-like)
ARNT aryl hydrocarbon receptor nuclear translocator
AXIN1 axin 1
CCNF cyclin F
CNBP CCHC-type zinc finger, nucleic acid binding protein
CSNK2A1 casein kinase 2, alpha 1 polypeptide
CTNNB1 catenin (cadherin-associated protein), beta 1, 88kDa
CXORF56 chromosome X open reading frame 56
CYCS cytochrome c, somatic
DKK1 dickkopf WNT signaling pathway inhibitor 1
DYNC2LI1 dynein, cytoplasmic 2, light intermediate chain 1
ERF Ets2 repressor factor
FOXG1 forkhead box G1
HESX1 HESX homeobox 1
HHEX hematopoietically expressed homeobox
HSD17B7 hydroxysteroid (17-beta) dehydrogenase 7
HSPA5 heat shock 70kDa protein 5 (glucose-regulated protein, 78kDa)
KIF20B kinesin family member 20B
LHX2 LIM homeobox 2
LIAS lipoic acid synthetase
LRP6 low density lipoprotein receptor-related protein 6
MBOAT7 membrane bound O-acyltransferase domain containing 7
MTOR mechanistic target of rapamycin (serine/threonine kinase)
NR2E1 nuclear receptor subfamily 2, group E, member 1
OTX2 orthodenticle homeobox 2
PAK1IP1 PAK1 interacting protein 1
PDPK1 3-phosphoinositide dependent protein kinase 1
PHGDH phosphoglycerate dehydrogenase
PIGN phosphatidylinositol glycan anchor biosynthesis, class N
SETD2 SET domain containing 2
SIX3 SIX homeobox 3
TCF7L1 transcription factor 7-like 1 (T-cell specific, HMG-box)
TDGF1 teratocarcinoma-derived growth factor 1
TMEM67 transmembrane protein 67
TULP3 tubby like protein 3
XPNPEP1 X-prolyl aminopeptidase (aminopeptidase P) 1, soluble