See et al., 2014 - SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy. Human molecular genetics   23(7):1754-70 Full text @ Hum. Mol. Genet.
35 Genes / Markers
Marker Type Symbol Name
Gene adgrl2a adhesion G protein-coupled receptor L2a
Gene bgna biglycan a
Gene chrna5 cholinergic receptor, nicotinic, alpha 5
Gene chrnb3b cholinergic receptor nicotinic beta 3 subunit b
Gene cript cysteine-rich PDZ-binding protein
Gene cxcr4b chemokine (C-X-C motif), receptor 4b
Gene cyth1b cytohesin 1b
Gene desma desmin a
Gene dnah9 dynein, axonemal, heavy chain 9
Gene dync1i2b dynein, cytoplasmic 1, intermediate chain 2b
Gene elp3 elongator acetyltransferase complex subunit 3
Gene ephb4a eph receptor B4a
Gene gemin2 gem (nuclear organelle) associated protein 2
Gene gfra2a GDNF family receptor alpha 2a
Gene igf1 insulin-like growth factor 1
Gene mef2aa myocyte enhancer factor 2aa
Gene mnx1 motor neuron and pancreas homeobox 1
Gene mnx2b motor neuron and pancreas homeobox 2b
Gene nes nestin
Gene nrxn2a neurexin 2a
Gene p2rx1 purinergic receptor P2X, ligand-gated ion channel, 1
Gene p2rx7 purinergic receptor P2X, ligand-gated ion channel, 7
Gene plek2 pleckstrin 2
Gene plxdc2b plexin domain containing 2b
Gene ptn pleiotrophin
Gene ptprk protein tyrosine phosphatase receptor type K
Gene rapsn receptor-associated protein of the synapse, 43kD
Gene scfd2 sec1 family domain containing 2
Gene smn1 survival of motor neuron 1, telomeric
Gene snx6 sorting nexin 6
Gene stat3 signal transducer and activator of transcription 3 (acute-phase response factor)
Gene syn2b synapsin IIb
Gene syngr1a synaptogyrin 1a
Gene ucp1 uncoupling protein 1
Gene utrn utrophin