RecName: Full=Homeobox protein aristaless-like 4

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Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4. [Am J Med Genet A. 2023]
Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.
Peled A, Sarig O, Mohamad J, Eskin-Schwartz M, Vodo D, Bochner R, Malchin N, Isakov O, Shomron N, Fainberg G, et al. Am J Med Genet A. 2023 Dec; 191(12):2806-2812. Epub 2023 Sep 19.
De novo ALX4 variant detected in child with non-syndromic craniosynostosis. [Braz J Med Biol Res. 2021]
De novo ALX4 variant detected in child with non-syndromic craniosynostosis.
Fonteles CS, Finnell RH, Lei Y, Zurita-Jimenez ME, Monteiro AJ, George TM, Harshbarger RJ. Braz J Med Biol Res. 2021; 54(11):e11396. Epub 2021 Sep 24.
Variants in ALX4 and their association with genitourinary defects. [Andrology. 2020]
Variants in ALX4 and their association with genitourinary defects.
Chen CH, Bournat JC, Wilken N, Rosenfeld JA, Zhang J, Seth A, Jorgez CJ. Andrology. 2020 Sep; 8(5):1243-1255. Epub 2020 Jul 16.

RefSeq genomic sequence
See the genomic reference sequence for the ALX4 gene (NG_015809.1).
RefSeq protein
See the reference protein sequence for homeobox protein aristaless-like 4 (NP_068745.2).

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Q9H161 [Domain Mapping of Disease Mut...]
Q9H161
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Homeobox protein aristaless-like 4
RecName: Full=Homeobox protein aristaless-like 4
gi|254763249|sp|Q9H161.2|ALX4_HUMAN

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