ectopic neuron Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description appearance of a neuron or group of neurons in a region where it is not normally found (Mammalian Phenotype Ontology, MP_0011723)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0011723
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Genes

36 gene mutations causing the ectopic neuron phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABL1 ABL proto-oncogene 1, non-receptor tyrosine kinase
ACP2 acid phosphatase 2, lysosomal
AKT3 v-akt murine thymoma viral oncogene homolog 3
APC2 adenomatosis polyposis coli 2
ARFGEF2 ADP-ribosylation factor guanine nucleotide-exchange factor 2 (brefeldin A-inhibited)
ASTN1 astrotactin 1
ATF2 activating transcription factor 2
ATM ATM serine/threonine kinase
B4GALT2 UDP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 2
CDK5R1 cyclin-dependent kinase 5, regulatory subunit 1 (p35)
CTNNA2 catenin (cadherin-associated protein), alpha 2
CXCR4 chemokine (C-X-C motif) receptor 4
DAB1 Dab, reelin signal transducer, homolog 1 (Drosophila)
EN1 engrailed homeobox 1
FYN FYN proto-oncogene, Src family tyrosine kinase
ISPD isoprenoid synthase domain containing
KCNJ6 potassium channel, inwardly rectifying subfamily J, member 6
KIF14 kinesin family member 14
LYST lysosomal trafficking regulator
MARCKS myristoylated alanine-rich protein kinase C substrate
MID1 midline 1
MYH10 myosin, heavy chain 10, non-muscle
PAFAH1B1 platelet-activating factor acetylhydrolase 1b, regulatory subunit 1 (45kDa)
PAX6 paired box 6
PLXNA2 plexin A2
PLXNB2 plexin B2
POMK protein-O-mannose kinase
POU1F1 POU class 1 homeobox 1
RB1 retinoblastoma 1
RELN reelin
RORA RAR-related orphan receptor A
RPL27A ribosomal protein L27a
SEMA4C sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4C
TOR1A torsin family 1, member A (torsin A)
UNC5C unc-5 homolog C (C. elegans)
ZNF423 zinc finger protein 423