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Phenotypic Alleles
Query Results -- Summary
 Symbol
Name
ID
Slc22a5
solute carrier family 22 (organic cation transporter), member 5
MGI:1329012

4 matching Alleles (1 Gene/Marker represented)
                                                              Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases Slc22a5jvs
solute carrier family 22 (organic cation transporter), member 5; juvenile visceral steatosis 11 jvs, Octn2 - Spontaneous cardiovascular, growth/size, homeostasis, liver/biliary, mortality/aging, renal/urinary, reproductive Carnitine Deficiency, Systemic Primary; CDSP 212140 Slc22a5Gt(OST21742)Lex
solute carrier family 22 (organic cation transporter), member 5; gene trap OST21742, Lexicon Genetics 11 Gene trapped
(Cell Line) Slc22a5tm1a(EUCOMM)Wtsi
solute carrier family 22 (organic cation transporter), member 5; targeted mutation 1a, Wellcome Trust Sanger Institute 11 Targeted (Floxed/Frt)
(Cell Line) Slc22a5tm1e(EUCOMM)Wtsi
solute carrier family 22 (organic cation transporter), member 5; targeted mutation 1e, Wellcome Trust Sanger Institute 11 Targeted (Reporter)
(Cell Line)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory