Symbol Name ID

Slc26a4 solute carrier family 26, member 4 MGI:1346029

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7 matching Alleles (1 Gene/Marker represented)

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                                                             Allele Symbol
Name                                                                Chr       Synonyms                   Category                                                Phenotypic Classes                                                                                Human Diseases                                             

Slc26a4loop
solute carrier family 26, member 4; loop
                                                                                           12   ABE028              Chemically induced (ENU)          behavior, hearing/vestibular/ear                                                                                                                                                               

Slc26a4pdsm
solute carrier family 26, member 4; Pendred's syndrome model
                                                                       12                       Spontaneous                       behavior, endocrine/exocrine, hearing/vestibular/ear, nervous system, reproductive     Pendred Syndrome; PDS 274600                                                                            

Slc26a4tm1.1Dontu
solute carrier family 26, member 4; targeted mutation 1.1, Department of Otolaryngology National Taiwan University Hospital
  12   Slc26a4tm1Dontuh    Targeted (knock-in)               behavior, hearing/vestibular/ear, nervous system                                       Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct; 600791                              

Slc26a4tm1Egr
solute carrier family 26, member 4; targeted mutation 1, Eric D Green                                                            12   Pds-, Slc26a4delta  Targeted (knock-out)              behavior, hearing/vestibular/ear, homeostasis, nervous system, pigmentation, skeleton  Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct; 600791; Pendred Syndrome; PDS 274600

Slc26a4tm1Sole
solute carrier family 26, member 4; targeted mutation 1, Manoocher Soleimani                                                    12                       Targeted (knock-out)              homeostasis, renal/urinary                                                                                                                                                                     

Slc26a4Gt(OST243055)Lex
solute carrier family 26, member 4; gene trap OST243055, Lexicon Genetics                                              12                       Gene trapped
(Cell Line)                                                                                                                                                                                                          

Slc26a4tm1a(KOMP)Wtsi
solute carrier family 26, member 4; targeted mutation 1a, Wellcome Trust Sanger Institute                                12                       Targeted (Floxed/Frt)
(Cell Line)