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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