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. Author manuscript; available in PMC: 2017 Jul 17.
Published in final edited form as: Mamm Genome. 2014 Feb 20;25(5-6):235–243. doi: 10.1007/s00335-014-9502-6

Table 3.

Genes with either stop codon gains or losses in either ILS or ISS strains

Genes with stop codon gains Genes with stop codon lost Function
ILS strain-specific
Ces1b Carboxylesterase activity
Nck2 Recruit and bind proteins involved in regulation of receptor protein kinases, and through these regulatory activities, this protein may be involved in cytoskeletal reorganization
Heatr7b1 Molecular binding
Olfr411 G-protein-coupled receptor activity and olfactory receptor activity
Mep1a Hydrolase activity and metal ion binding
AMY2B Hydrolyze 1,4-alpha-glucoside bonds in oligosaccharides and polysaccharides, and thus catalyze the first step in digestion of dietary starch and glycogen
Zbtb5 Zinc finger and BTB domain-containing protein 5
Aurkc ATP binding, kinase activity, possible role in oocytes and microtubules organization with the cetrozome during mitosis, and is over expressed in cancer cell lines
Mrgprx2 G-protein-coupled receptor activity and neuropeptide binding
Oca2 Arsenite trasnsmembrane activity
Defb46 Antimicrobial peptide implicated in the resistance of epithelial surfaces to microbial colonization
Vmn2r100 G-protein-coupled receptor
Tmem100 Developmental protein
lfi205 Interferon activated gene 205
Znhit3 Thyroid receptor-interacting protein
Scnm1 Plays a role in RNA splicing, may contribute to the recognition of nonconsensus donor sites
Vmn2r114 G-protein-coupled receptor
ISS strain-specific
Krt42 Structural molecule activity
Tubb4b GTPase activity and binding
Sipa 1l2 Gap activity for Ras-related regulatory protiens Rap1 and Rap2
Prex1 Guanine-nucleotide-releasing factor
Hbq1b Heme binding, oxygen binding
Morn4 Unknown
Mnda Participates in blood cell-specific responses to interferons

Gene symbols are listed for those genes that show either a stop codon gain or loss in either the ILS or ISS strains. Functions were obtained from GeneCards’ Weizmann Institute of Science, UniProt, and MGI Mouse Genome Informatic, Jackson Labs