collagen alpha-3(IX) chain isoform X3 [Homo sapiens]

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A novel missense COL9A3 variant in a pedigree with multiple lumbar disc herniation. [J Orthop Surg Res. 2024]
A novel missense COL9A3 variant in a pedigree with multiple lumbar disc herniation.
Jiang L, Wang C, Ye Z, Hu Q. J Orthop Surg Res. 2024 Jan 3; 19(1):19. Epub 2024 Jan 3.
Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome. [Orphanet J Rare Dis. 2022]
Identification of three novel homozygous variants in COL9A3 causing autosomal recessive Stickler syndrome.
Rad A, Najafi M, Suri F, Abedini S, Loum S, Karimiani EG, Daftarian N, Murphy D, Doosti M, Moghaddasi A, et al. Orphanet J Rare Dis. 2022 Mar 3; 17(1):97. Epub 2022 Mar 3.
Heterozygous COL9A3 variants cause severe peripheral vitreoretinal degeneration and retinal detachment. [Eur J Hum Genet. 2021]
Heterozygous COL9A3 variants cause severe peripheral vitreoretinal degeneration and retinal detachment.
Nash BM, Watson CJG, Hughes E, Hou AL, Loi TH, Bennetts B, Jelovic D, Polkinghorne PJ, Gorbatov M, Grigg JR, et al. Eur J Hum Genet. 2021 May; 29(5):881-886. Epub 2021 Feb 25.

RefSeq genomic sequence
See the genomic reference sequence for the COL9A3 gene (NG_016353.1).
RefSeq mRNA
See reference mRNA sequence for the COL9A3 gene (XM_017027666.2).

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Homo sapiens neurotensin (NTS), mRNA
Homo sapiens neurotensin (NTS), mRNA
gi|1519311949|ref|NM_006183.5|

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