Mapping Data Summary

• Symbol: Trpm5
• Name: transient receptor potential cation channel, subfamily M, member 5
• ID: MGI:1861718
• Chromosome: 7

7 mapping experiments

Experiment Type	Details	Chromosome	Reference
TEXT		7	J:108174 Ruf N, et al., Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes. Genomics. 2006 Apr;87(4):509-19
TEXT-Physical Mapping		7	J:65815 Engemann S, et al., Sequence and functional comparison in the beckwith-wiedemann region: implications for a novel imprinting centre and extended imprinting. Hum Mol Genet. 2000 Nov 1;9(18):2691-706
TEXT-Physical Mapping		7	J:63607 Enklaar T, et al., Mtr1, a novel biallelically expressed gene in the center of the mouse distal chromosome 7 imprinting cluster, is a member of the Trp gene family. Genomics. 2000 Jul 15;67(2):179-87
TEXT-Physical Mapping		7	J:79882 Fitzpatrick GV, et al., Regional loss of imprinting and growth deficiency in mice with a targeted deletion of KvDMR1. Nat Genet. 2002 Nov;32(3):426-31
TEXT-Physical Mapping		7	J:65742 Onyango P, et al., Sequence and comparative analysis of the mouse 1-megabase region orthologous to the human 11p15 imprinted domain. Genome Res. 2000 Nov;10(11):1697-710
TEXT-Physical Mapping		7	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-Physical Mapping		7	J:63552 Yatsuki H, et al., Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human. DNA Res. 2000 Jun 30;7(3):195-206