Symbol Name ID

Slc26a4 solute carrier family 26, member 4 MGI:1346029

---

3 matching Alleles (1 Gene/Marker represented)

---

                                                             Allele Symbol
Name                                                                Chr       Synonyms             Category                                          Phenotypic Classes                                                                                Human Diseases                                             

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