Mus musculus Usher syndrome 1G homolog (human), mRNA (cDNA clone MGC:1 - Nucleotide

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Spontaneous allelic variant in deafness-blindness gene Ush1g resulting in an expanded phenotype. [Genes Brain Behav. 2023]
Spontaneous allelic variant in deafness-blindness gene Ush1g resulting in an expanded phenotype.
Vartanian V, Krey JF, Chatterjee P, Curtis A, Six M, Rice SPM, Jones SM, Sampath H, Allen CN, Ryals RC, et al. Genes Brain Behav. 2023 Aug; 22(4):e12849. Epub 2023 Jun 16.
Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane. [Proc Natl Acad Sci U S A. 2019]
Otogelin, otogelin-like, and stereocilin form links connecting outer hair cell stereocilia to each other and the tectorial membrane.
Avan P, Le Gal S, Michel V, Dupont T, Hardelin JP, Petit C, Verpy E. Proc Natl Acad Sci U S A. 2019 Dec 17; 116(51):25948-25957. Epub 2019 Nov 27.
SANS (USH1G) Molecularly Links the Human Usher Syndrome Protein Network to the Intraflagellar Transport Module by Direct Binding to IFT-B Proteins. [Front Cell Dev Biol. 2019]
SANS (USH1G) Molecularly Links the Human Usher Syndrome Protein Network to the Intraflagellar Transport Module by Direct Binding to IFT-B Proteins.
Sorusch N, Yildirim A, Knapp B, Janson J, Fleck W, Scharf C, Wolfrum U. Front Cell Dev Biol. 2019; 7:216. Epub 2019 Oct 4.

RefSeq alternative splicing
See 2 reference mRNA sequence splice variants for the Ush1g gene.

Ush1g [Mouse Genome Informatics (MGI)]
Ush1g
Mouse Genome Informatics (MGI)
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome
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K.K. DNAFORM

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Nucleotide