Homo sapiens kynureninase (L-kynurenine hydrolase), mRNA (cDNA clone M - Nucleotide

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Congenital NAD Deficiency Disorder. [GeneReviews(®). 1993]
Congenital NAD Deficiency Disorder.
Mark P, Dunwoodie S. GeneReviews(®). 1993-2024. 2023 Jul 27
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery. [Nat Commun. 2022]
Scalable multiplex co-fractionation/mass spectrometry platform for accelerated protein interactome discovery.
Havugimana PC, Goel RK, Phanse S, Youssef A, Padhorny D, Kotelnikov S, Kozakov D, Emili A. Nat Commun. 2022 Jul 13; 13(1):4043. Epub 2022 Jul 13.
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.

RefSeq alternative splicing
See 12 reference mRNA sequence splice variants for the KYNU gene.

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

uncharacterized protein C4orf17 homolog isoform 2 [Mus musculus]
uncharacterized protein C4orf17 homolog isoform 2 [Mus musculus]
gi|254281184|ref|NP_001156858.1|

Protein

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Nucleotide