Linder et al., 2011 - Systemic splicing factor deficiency causes tissue-specific defects: A zebrafish model for Retinitis pigmentosa. Human molecular genetics   20(2):368-377 Full text @ Hum. Mol. Genet.
19 Genes / Markers
Marker Type Symbol Name
Gene crx cone-rod homeobox
Gene gnat1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1
Gene gnat2 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 2
Gene irx6a iroquois homeobox 6a
Gene lsm7 LSM7 homolog, U6 small nuclear RNA and mRNA degradation associated
Gene myf5 myogenic factor 5
Gene myod1 myogenic differentiation 1
Gene opn1lw1 opsin 1 (cone pigments), long-wave-sensitive, 1
Gene opn1lw2 opsin 1 (cone pigments), long-wave-sensitive, 2
Gene opn1mw1 opsin 1 (cone pigments), medium-wave-sensitive, 1
Gene pax2a paired box 2a
Gene pcna proliferating cell nuclear antigen
Gene prpf4 PRP4 pre-mRNA processing factor 4 homolog (yeast)
Gene prpf31 PRP31 pre-mRNA processing factor 31 homolog (yeast)
Gene rcvrn2 recoverin 2
Gene rho rhodopsin
Gene rx3 retinal homeobox gene 3
Gene smn1 survival of motor neuron 1, telomeric
Gene snrpc small nuclear ribonucleoprotein polypeptide C