KIAA0442 [Homo sapiens]

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Isolated loss of the AUTS2 long isoform, brain-wide or targeted to Calbindin-lineage cells, generates a specific suite of brain, behavioral, and molecular pathologies. [Genetics. 2024]
Isolated loss of the AUTS2 long isoform, brain-wide or targeted to Calbindin-lineage cells, generates a specific suite of brain, behavioral, and molecular pathologies.
Song Y, Seward CH, Chen CY, LeBlanc A, Leddy AM, Stubbs L. Genetics. 2024 Jan 3; 226(1).
Structural polymorphism driven by a register shift in a CGAG-rich region found in the promoter of the neurodevelopmental regulator AUTS2 gene. [Nucleic Acids Res. 2023]
Structural polymorphism driven by a register shift in a CGAG-rich region found in the promoter of the neurodevelopmental regulator AUTS2 gene.
Novotný A, Plavec J, Kocman V. Nucleic Acids Res. 2023 Apr 11; 51(6):2602-2613.
Cerebral organoids containing an AUTS2 missense variant model microcephaly. [Brain. 2023]
Cerebral organoids containing an AUTS2 missense variant model microcephaly.
Fair SR, Schwind W, Julian DL, Biel A, Guo G, Rutherford R, Ramadesikan S, Westfall J, Miller KE, Kararoudi MN, et al. Brain. 2023 Jan 5; 146(1):387-404.

RefSeq genomic sequence
See the genomic reference sequence for the AUTS2 gene (NG_034133.1).
RefSeq protein isoforms
See 55 reference sequence protein isoforms for the AUTS2 gene.

Nucleotide
Nucleotide sequence from coding region
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DB452430 RIKEN full-length enriched human cDNA library, testis Homo sapiens cDNA...
DB452430 RIKEN full-length enriched human cDNA library, testis Homo sapiens cDNA clone H013057H20 5', mRNA sequence
gi|92056715|gnl|dbEST|38447715|dbj| 430.1|

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Protein