PREDICTED: Homo sapiens ankyrin repeat and fibronectin type III domain - Nucleotide

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Ankfn1-mutant vestibular defects require loss of both ancestral and derived paralogs for penetrance in zebrafish. [G3 (Bethesda). 2022]
Ankfn1-mutant vestibular defects require loss of both ancestral and derived paralogs for penetrance in zebrafish.
Ross KD, Ren J, Zhang R, Chi NC, Hamilton BA. G3 (Bethesda). 2022 Mar 4; 12(3).
Human gingiva transcriptome during wound healing. [J Clin Periodontol. 2017]
Human gingiva transcriptome during wound healing.
Wang Y, Tatakis DN. J Clin Periodontol. 2017 Apr; 44(4):394-402. Epub 2017 Feb 11.
A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease. [PLoS One. 2013]
A possible mechanism behind autoimmune disorders discovered by genome-wide linkage and association analysis in celiac disease.
Östensson M, Montén C, Bacelis J, Gudjonsdottir AH, Adamovic S, Ek J, Ascher H, Pollak E, Arnell H, Browaldh L, et al. PLoS One. 2013; 8(8):e70174. Epub 2013 Aug 2.

RefSeq alternative splicing
See 28 reference mRNA sequence splice variants for the ANKFN1 gene.
RefSeq protein product
See the reference protein sequence for ankyrin repeat and fibronectin type-III domain-containing protein 1 isoform X4 (XP_011522731.1).

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Protein
Protein sequence from Nucleotide coding region
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Ensembl [Ensembl]
Ensembl
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
Order Ankfn1 cDNA clone/Protein/Antibody/RNAi [OriGene]
Order Ankfn1 cDNA clone/Protein/Antibody/RNAi
OriGene

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Nucleotide