abnormal neuronal precursor cell number Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the normal count of the neuroblast embryonic cells that develop into nerve cells or neurons (Mammalian Phenotype Ontology, MP_0004979)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004979
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Genes

33 gene mutations causing the abnormal neuronal precursor cell number phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CCKAR cholecystokinin A receptor
CDKN1A cyclin-dependent kinase inhibitor 1A (p21, Cip1)
CHD7 chromodomain helicase DNA binding protein 7
CNTF ciliary neurotrophic factor
DAGLA diacylglycerol lipase, alpha
DLL1 delta-like 1 (Drosophila)
DMRTA2 DMRT-like family A2
ERBB2 erb-b2 receptor tyrosine kinase 2
FST follistatin
GAS1 growth arrest-specific 1
GDF11 growth differentiation factor 11
JAG1 jagged 1
KIF20B kinesin family member 20B
LLGL1 lethal giant larvae homolog 1 (Drosophila)
LMX1B LIM homeobox transcription factor 1, beta
LRRK2 leucine-rich repeat kinase 2
NEIL3 nei endonuclease VIII-like 3 (E. coli)
NES nestin
NEUROG2 neurogenin 2
NKX2-8 NK2 homeobox 8
NPY1R neuropeptide Y receptor Y1
NPY2R neuropeptide Y receptor Y2
PHOX2B paired-like homeobox 2b
POU3F2 POU class 3 homeobox 2
PSEN1 presenilin 1
PTBP2 polypyrimidine tract binding protein 2
PTCH1 patched 1
PTF1A pancreas specific transcription factor, 1a
RBL1 retinoblastoma-like 1
SMO smoothened, frizzled class receptor
TP53 tumor protein p53
TP53BP2 tumor protein p53 binding protein 2
ZBTB18 zinc finger and BTB domain containing 18