proteasome subunit p58 [Homo sapiens]

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PSMD3 gene mutations cause pathological myopia. [J Med Genet. 2023]
PSMD3 gene mutations cause pathological myopia.
Chen J, Lian P, Zhao X, Li J, Yu X, Huang X, Chen S, Lu L. J Med Genet. 2023 Sep; 60(9):918-924. Epub 2023 Mar 22.
Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C. [Hum Genet. 2015]
Genome-wide association study identifies a PSMD3 variant associated with neutropenia in interferon-based therapy for chronic hepatitis C.
Iio E, Matsuura K, Nishida N, Maekawa S, Enomoto N, Nakagawa M, Sakamoto N, Yatsuhashi H, Kurosaki M, Izumi N, et al. Hum Genet. 2015 Mar; 134(3):279-89. Epub 2014 Dec 17.
Genetic variants at PSMD3 interact with dietary fat and carbohydrate to modulate insulin resistance. [J Nutr. 2013]
Genetic variants at PSMD3 interact with dietary fat and carbohydrate to modulate insulin resistance.
Zheng JS, Arnett DK, Parnell LD, Lee YC, Ma Y, Smith CE, Richardson K, Li D, Borecki IB, Ordovas JM, et al. J Nutr. 2013 Mar; 143(3):354-61. Epub 2013 Jan 9.

RefSeq protein
See the reference protein sequence for 26S proteasome non-ATPase regulatory subunit 3 (NP_002800.2).

Nucleotide
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Protein