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Symbol
Name
ID
Chromosome
Drg2
developmentally regulated GTP binding protein 2
MGI:1342307
11
4 mapping experiments
Experiment Type Details Chromosome Reference
TEXT 11 J:125240 Yan J, et al., Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike. Am J Hum Genet. 2007 Mar;80(3):518-25
TEXT-Physical Mapping 11 J:58614 Liang Y, et al., Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2. Genomics. 1999 Nov 1;61(3):243-58
TEXT-Physical Mapping 11 J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
TEXT-Radiation Hybrid 11 J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;

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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory