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Phenotypic Alleles
Query Results -- Summary
 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
images 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
images 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

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