BTB/POZ domain-containing protein KCTD1 isoform 1 [Mus musculus]

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Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies. [Int J Mol Sci. 2024]
Genetic Variants in KCTD1 Are Associated with Isolated Dental Anomalies.
Ruangchan C, Ngamphiw C, Krasaesin A, Intarak N, Tongsima S, Kaewgahya M, Kawasaki K, Mahawong P, Paripurana K, Sookawat B, et al. Int J Mol Sci. 2024 May 9; 25(10). Epub 2024 May 9.
KCTD1 and Scalp-Ear-Nipple ('Finlay-Marks') syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains. [Ophthalmic Genet. 2023]
KCTD1 and Scalp-Ear-Nipple ('Finlay-Marks') syndrome may be associated with myopia and Thin basement membrane nephropathy through an effect on the collagen IV α3 and α4 chains.
Wang D, Trevillian P, May S, Diakumis P, Wang Y, Colville D, Bahlo M, Greferath U, Fletcher E, Young B, et al. Ophthalmic Genet. 2023 Feb; 44(1):19-27. Epub 2022 Dec 29.
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 (I27N) mutant mice. [J Biomed Sci. 2017]
Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 (I27N) mutant mice.
Kumar S, Rathkolb B, Sabrautzki S, Krebs S, Kemter E, Becker L, Beckers J, Bekeredjian R, Brommage R, Calzada-Wack J, et al. J Biomed Sci. 2017 Aug 17; 24(1):57. Epub 2017 Aug 17.

RefSeq mRNA
See reference mRNA sequence for the Kctd1 gene (NM_001142731.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the Kctd1 gene.

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Ensembl
Ensembl [Ensembl]
Ensembl
Ensembl [Ensembl]
Ensembl
GlyGen glycoinformatics resource [GlyGen glycoinformatics resou...]
GlyGen glycoinformatics resource
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

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Protein