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Search results 501 to 506 out of 506 for Slc12a2

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Type

Details

Score

Allele

Slc12a2<em1Smoc> | MGI:7292356

Name:	solute carrier family 12, member 2; endonuclease-mediated mutation 1, Shanghai Model Organisms Center
Allele Type:	Endonuclease-mediated
Attribute String:	Reporter

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Strain

MGI:6771158 | C57BL/6JSmoc-Slc12a2<em1Smoc>/Smoc

Attribute String:

coisogenic, endonuclease-mediated mutation, mutant strain

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Publication

32658972 | -

First Author:	McNeill A
Year:	2020
Journal:	Brain
Title:	SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect.
Volume:	143
Issue:	8
Pages:	2380-2387

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Publication

32294086 | -

First Author:	Mutai H
Year:	2020
Journal:	PLoS Genet
Title:	Variants encoding a restricted carboxy-terminal domain of SLC12A2 cause hereditary hearing loss in humans.
Volume:	16
Issue:	4
Pages:	e1008643

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DO Term

DOID:0112159 | autosomal dominant nonsyndromic deafness 78

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Publication

15320950 | J:101834

First Author:	Wangemann P
Year:	2004
Journal:	BMC Med
Title:	Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model.
Volume:	2

Pages:	30

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