otogelin isoform a precursor [Homo sapiens]

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An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population. [Hum Genet. 2024]
An overload of missense variants in the OTOG gene may drive a higher prevalence of familial Meniere disease in the European population.
Parra-Perez AM, Gallego-Martinez A, Lopez-Escamez JA. Hum Genet. 2024 Mar; 143(3):423-435. Epub 2024 Mar 22.
Prediction and interpretation of rare missense variant in OTOG associated with hearing loss. [Genomics. 2021]
Prediction and interpretation of rare missense variant in OTOG associated with hearing loss.
Askari M, Moradi Z, Mohammadi M, Lagzian M, Asgharzade S. Genomics. 2021 Jul; 113(4):2793-2799. Epub 2021 Jun 9.
Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease. [Ear Hear. 2020]
Burden of Rare Variants in the OTOG Gene in Familial Meniere's Disease.
Roman-Naranjo P, Gallego-Martinez A, Soto-Varela A, Aran I, Moleon MDC, Espinosa-Sanchez JM, Amor-Dorado JC, Batuecas-Caletrio A, Perez-Vazquez P, Lopez-Escamez JA. Ear Hear. 2020 Nov/Dec; 41(6):1598-1605.

RefSeq genomic sequence
See the genomic reference sequence for the OTOG gene (NG_033191.2).
RefSeq mRNA
See reference mRNA sequence for the OTOG gene (NM_001277269.2).
RefSeq protein isoforms
See the other reference sequence protein isoform for the OTOG gene (NP_001278992.1).

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Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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