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Name barttin CLCNK type accessory beta subunit
Synonyms Bartter syndrome, infantile, with sensorineural deafness (Barttin)
Species Mouse
Chromosome 4
MGI MGI:2153465
NCBI 140475
Ensembl ENSMUSG00000025418
VEGA OTTMUSG00000008195
HGNC HGNC:16512
Homologene 14291
CCDS CCDS18419.1
UCSC Chr4:106340653-106349440
IMPC Google Entrez PubMed IMSR
Gene Ontology BioGPS Gene Cloud IGTC Mouse Phenome DB
Mouse Mine KOMP Phenotyping Monarch GeneCards ClinGen

ES cell line

MMRRC ID Strain Name
52865 KOMP ES cell line Bsndtm2a(KOMP)Wtsi
52866 KOMP ES cell line Bsndtm1a(KOMP)Wtsi

Other

MMRRC ID Strain Name
39393 C57BL/6J-MtgxR1327Btlr/Mmmh
39891 C57BL/6J-MtgxR1869Btlr/Mmmh
39930 C57BL/6J-MtgxR1912Btlr/Mmmh
41083 C57BL/6J-MtgxR4294Btlr/Mmmh
41693 C57BL/6J-MtgxR4411Btlr/Mmmh
42812 C57BL/6J-MtgxR5241Btlr/Mmmh
43193 C57BL/6J-MtgxR5733Btlr/Mmmh
44444 C57BL/6J-MtgxR6274Btlr/Mmmh
44615 C57BL/6J-MtgxR6483Btlr/Mmmh
45236 C57BL/6J-MtgxR7184Btlr/Mmmh
45255 C57BL/6J-MtgxR7153Btlr/Mmmh

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