Homo sapiens 3-hydroxyanthranilate 3,4-dioxygenase, mRNA (cDNA clone M - Nucleotide

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Congenital NAD Deficiency Disorder. [GeneReviews(®). 1993]
Congenital NAD Deficiency Disorder.
Mark P, Dunwoodie S. GeneReviews(®). 1993-2025. 2023 Jul 27
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation. [Birth Defects Res. 2022]
Re-sequencing of candidate genes FOXF1, HSPA6, HAAO, and KYNU in 522 individuals with VATER/VACTERL, VACTER/VACTERL-like association, and isolated anorectal malformation.
Thiem CE, Stegmann JD, Hilger AC, Waffenschmidt L, Bendixen C, Köllges R, Schmiedeke E, Schäfer FM, Lacher M, Kosch F, et al. Birth Defects Res. 2022 Jun; 114(10):478-486. Epub 2022 Mar 31.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome. [Cell. 2021]
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Huttlin EL, Bruckner RJ, Navarrete-Perea J, Cannon JR, Baltier K, Gebreab F, Gygi MP, Thornock A, Zarraga G, Tam S, et al. Cell. 2021 May 27; 184(11):3022-3040.e28. Epub 2021 May 6.

RefSeq alternative splicing
See 5 reference mRNA sequence splice variants for the HAAO gene.

reagents [ExactAntigen/Labome]
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Order full-length cDNA clone [K.K. DNAFORM]
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Nucleotide