Mapping Data Summary

• Symbol: Slc22a18
• Name: solute carrier family 22 (organic cation transporter), member 18
• ID: MGI:1336884
• Chromosome: 7

15 mapping experiments

Experiment Type	Details	Chromosome	Reference
FISH		7	J:52861 Day CD, et al., The imprinted domain in mouse distal Chromosome 7: reagents for mutagenesis and sequencing. Mamm Genome. 1999 Feb;10(2):182-5
TEXT		7	J:72512 Choi JD, et al., Microarray expression profiling of tissues from mice with uniparental duplications of Chromosomes 7 and 11 to identify imprinted genes. Mamm Genome. 2001 Oct;12(10):758-64
TEXT-Genetic Cross		7	J:46790 Dao D, et al., IMPT1, an imprinted gene similar to polyspecific transporter and multi-drug resistance genes. Hum Mol Genet. 1998 Apr;7(4):597-608
TEXT-Physical Mapping		7	J:52790 Ainscough JF, et al., Mechanism of imprinting on mouse distal chromosome 7. Genet Res. 1998 Dec;72(3):237-45
TEXT-Physical Mapping		7	J:47762 Cooper PR, et al., Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15.5 imprinted domain. Genomics. 1998 Apr 1;49(1):38-51
TEXT-Physical Mapping		7	J:52861 Day CD, et al., The imprinted domain in mouse distal Chromosome 7: reagents for mutagenesis and sequencing. Mamm Genome. 1999 Feb;10(2):182-5
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: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:66461 Kato R, et al., Sequence-ready 1-Mb YAC, BAC and cosmid contigs covering the distal imprinted region of mouse chromosome 7. DNA Res. 1999 Dec 31;6(6):401-5
TEXT-Physical Mapping		7	J:80758 Mahy NL, et al., Gene density and transcription influence the localization of chromatin outside of chromosome territories detectable by FISH. J Cell Biol. 2002 Dec 9;159(5):753-63
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:93878 Salas M, et al., Placental growth retardation due to loss of imprinting of Phlda2. Mech Dev. 2004 Oct;121(10):1199-210
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
TEXT-Radiation Hybrid		7	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;