integrator complex subunit 11 isoform X3 [Homo sapiens]

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A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder. [Cell Rep. 2023]
A homozygous variant in INTS11 links mitosis and neurogenesis defects to a severe neurodevelopmental disorder.
Kuang H, Li Y, Wang Y, Shi M, Duan R, Xiao Q, She H, Liu Y, Liang Q, Teng Y, et al. Cell Rep. 2023 Dec 26; 42(12):113445. Epub 2023 Nov 18.
Bi-allelic variants in INTS11 are associated with a complex neurological disorder. [Am J Hum Genet. 2023]
Bi-allelic variants in INTS11 are associated with a complex neurological disorder.
Tepe B, Macke EL, Niceta M, Weisz Hubshman M, Kanca O, Schultz-Rogers L, Zarate YA, Schaefer GB, Granadillo De Luque JL, Wegner DJ, et al. Am J Hum Genet. 2023 May 4; 110(5):774-789. Epub 2023 Apr 12.
An examination of the metal ion content in the active sites of human endonucleases CPSF73 and INTS11. [J Biol Chem. 2023]
An examination of the metal ion content in the active sites of human endonucleases CPSF73 and INTS11.
Huang J, Liu X, Sun Y, Li Z, Lin MH, Hamilton K, Mandel CR, Sandmeir F, Conti E, Oyala PH, et al. J Biol Chem. 2023 Apr; 299(4):103047. Epub 2023 Feb 22.

RefSeq mRNA
See reference mRNA sequence for the INTS11 gene (XM_054337268.1).
RefSeq protein isoforms
See 11 reference sequence protein isoforms for the INTS11 gene.

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Protein