RecName: Full=LisH domain-containing protein ARMC9; AltName: Full=Arma - Protein

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Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients. [Ocul Immunol Inflamm. 2019]
Association Study of ARMC9 Gene Variants with Vogt-Koyanagi-Harada Disease in Japanese Patients.
Ohno T, Meguro A, Takeuchi M, Yamane T, Teshigawara T, Kitaichi N, Horie Y, Namba K, Ohno S, Nakao K, et al. Ocul Immunol Inflamm. 2019; 27(5):699-705. Epub 2018 Nov 5.
Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly. [Am J Med Genet A. 2018]
Whole exome sequencing reveals a mutation in ARMC9 as a cause of mental retardation, ptosis, and polydactyly.
Kar A, Phadke SR, Das Bhowmik A, Dalal A. Am J Med Genet A. 2018 Jan; 176(1):34-40. Epub 2017 Nov 21.
Tumor antigens isolated from a patient with vitiligo and T-cell-infiltrated melanoma. [Cancer Res. 2001]
Tumor antigens isolated from a patient with vitiligo and T-cell-infiltrated melanoma.
Kiniwa Y, Fujita T, Akada M, Ito K, Shofuda T, Suzuki Y, Yamamoto A, Saida T, Kawakami Y. Cancer Res. 2001 Nov 1; 61(21):7900-7.

RefSeq protein isoforms
See 9 reference sequence protein isoforms for the ARMC9 gene.

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Q7Z3E5 [Domain Mapping of Disease Mut...]
Q7Z3E5
Domain Mapping of Disease Mutations
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein