Mapping Data Summary

• Symbol: Cln8
• Name: CLN8 transmembrane ER and ERGIC protein
• ID: MGI:1349447
• Chromosome: 8

7 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	8	J:39060 Chang B, et al., Improved genetic map for the mnd gene, using the retinal degeneration aspect of the phenotype. MGI Direct Data Submission. 1998;
CROSS	Cross Type: Intercross	8	J:1224 Messer A, et al., Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS). Genomics. 1992 Jul;13(3):797-802
TEXT		8	J:1224 Messer A, et al., Mapping of the motor neuron degeneration (Mnd) gene, a mouse model of amyotrophic lateral sclerosis (ALS). Genomics. 1992 Jul;13(3):797-802
TEXT-Physical Mapping		8	J:57766 Ranta S, et al., The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8. Nat Genet. 1999 Oct;23(2):233-6
TEXT-QTL		8	J:67793 Encinas JA, et al., Identification of genetic loci associated with paralysis, inflammation and weight loss in mouse experimental autoimmune encephalomyelitis. Int Immunol. 2001 Mar;13(3):257-64
TEXT-Radiation Hybrid		8	J:57766 Ranta S, et al., The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8. Nat Genet. 1999 Oct;23(2):233-6
TEXT-Radiation Hybrid		8	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;