Homo sapiens distal-less homeobox 3 (DLX3), RefSeqGene on chromosome 1 - Nucleotide

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A novel DLX3 mutation causes tricho-dento-osseous syndrome with abnormal enamel structure and formation. [Arch Oral Biol. 2024]
A novel DLX3 mutation causes tricho-dento-osseous syndrome with abnormal enamel structure and formation.
Quan J, Liu Y, Ji L, Zhao Y, Zheng S. Arch Oral Biol. 2024 Jan; 157:105849. Epub 2023 Nov 13.
A heterozygous missense variant in DLX3 leads to uterine leiomyomas and pregnancy losses in a consanguineous Iranian family. [Gene. 2023]
A heterozygous missense variant in DLX3 leads to uterine leiomyomas and pregnancy losses in a consanguineous Iranian family.
Saboori-Darabi S, Carrera P, Akbari A, Amiri-Yekta A, Almadani N, Battista Pipitone G, Shahrokh-Tehraninejad E, Lotfi M, Mazaheri M, Totonchi M. Gene. 2023 May 20; 865:147292. Epub 2023 Feb 26.
A comprehensive SARS-CoV-2-human protein-protein interactome reveals COVID-19 pathobiology and potential host therapeutic targets. [Nat Biotechnol. 2023]
A comprehensive SARS-CoV-2-human protein-protein interactome reveals COVID-19 pathobiology and potential host therapeutic targets.
Zhou Y, Liu Y, Gupta S, Paramo MI, Hou Y, Mao C, Luo Y, Judd J, Wierbowski S, Bertolotti M, et al. Nat Biotechnol. 2023 Jan; 41(1):128-139. Epub 2022 Oct 10.

Protein
Protein sequence from Nucleotide coding region
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Nucleotide