protein dopey-2 isoform X1 [Homo sapiens]

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A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family. [Mol Vis. 2020]
A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family.
Darbari E, Zare-Abdollahi D, Alavi A, Rezaei Kanavi M, Feizi S, Hosseini SB, Baradaran-Rafii A, Ahmadieh H, Issazadeh-Navikas S, Elahi E. Mol Vis. 2020; 26:757-765. Epub 2020 Nov 25.
A quantitative assessment of gene expression (QAGE) reveals differential overexpression of DOPEY2, a candidate gene for mental retardation, in Down syndrome brain regions. [Int J Dev Neurosci. 2009]
A quantitative assessment of gene expression (QAGE) reveals differential overexpression of DOPEY2, a candidate gene for mental retardation, in Down syndrome brain regions.
Rachidi M, Delezoide AL, Delabar JM, Lopes C. Int J Dev Neurosci. 2009 Jun; 27(4):393-8. Epub 2009 Feb 13.
C21orf5, a human candidate gene for brain abnormalities and mental retardation in Down syndrome. [Cytogenet Genome Res. 2006]
C21orf5, a human candidate gene for brain abnormalities and mental retardation in Down syndrome.
Rachidi M, Lopes C, Delezoide AL, Delabar JM. Cytogenet Genome Res. 2006; 112(1-2):16-22.

RefSeq mRNA
See reference mRNA sequence for the DOP1B gene (XM_054324968.1).
RefSeq protein isoforms
See 4 reference sequence protein isoforms for the DOP1B gene.

Miopithecus talapoin myxovirus resistance 2 protein (Mx2) mRNA, partial cds
Miopithecus talapoin myxovirus resistance 2 protein (Mx2) mRNA, partial cds
gi|948542522|gb|KT698244.1|

Nucleotide

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Protein