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Table 1 Protein coding genes situated within the 1.3 Mb critical region. An asterisk (*) highlights genes previously associated with, or within a gene family associated with retinal degeneration in humans

From: A LINE-1 insertion situated in the promoter of IMPG2 is associated with autosomal recessive progressive retinal atrophy in Lhasa Apso dogs

Gene Name Abbreviation
ABI family member 3 binding protein AB13BP
Interphotoreceptor matrix proteoglycan 2 IMPG2*
SUMO1/sentrin specific peptidase 7 SENP7
tRNA methyltransferase 10C, mitochondrial RNase P subunit TRMT10C
PEST proteolytic signal containing nuclear protein PCNP
Zinc finger and BTB domain containing 11 ZBTB11
Centrosomal protein 97 CEP97*
Neurexophilin and PC-esterase domain family member 3 NXPE3
NFKB inhibitor zeta NFKBIZ
Zona pellucida like domain containing 1 ZPLD1
ENSCAFG00000009584 N/A; no human orthologue
Ribosomal protein L24 RPL24