axin-1 isoform X11 [Homo sapiens]

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AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia. [Am J Hum Genet. 2023]
AXIN1 bi-allelic variants disrupting the C-terminal DIX domain cause craniometadiaphyseal osteosclerosis with hip dysplasia.
Terhal P, Venhuizen AJ, Lessel D, Tan WH, Alswaid A, Grün R, Alzaidan HI, von Kroge S, Ragab N, Hempel M, et al. Am J Hum Genet. 2023 Sep 7; 110(9):1470-1481. Epub 2023 Aug 14.
The Axin scaffold protects the kinase GSK3β from cross-pathway inhibition. [Elife. 2023]
The Axin scaffold protects the kinase GSK3β from cross-pathway inhibition.
Gavagan M, Jameson N, Zalatan JG. Elife. 2023 Aug 7; 12. Epub 2023 Aug 7.
Association between AXIN1 gene polymorphism (rs9921222) of WNT signaling pathway and susceptibility to osteoporosis in Egyptian patients: a case-control study. [BMC Musculoskelet Disord. 2023]
Association between AXIN1 gene polymorphism (rs9921222) of WNT signaling pathway and susceptibility to osteoporosis in Egyptian patients: a case-control study.
Nassar ES, Elnemr R, Shaaban A, Elhameed AA, Taleb RSZ. BMC Musculoskelet Disord. 2023 Jun 28; 24(1):527. Epub 2023 Jun 28.

RefSeq genomic sequence
See the genomic reference sequence for the AXIN1 gene (NG_012267.1).
RefSeq mRNA
See reference mRNA sequence for the AXIN1 gene (XM_054314079.1).
RefSeq protein isoforms
See 17 reference sequence protein isoforms for the AXIN1 gene.

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Protein