RecName: Full=Protein furry homolog-like; AltName: Full=ALL1-fused gen - Protein

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De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features. [Am J Hum Genet. 2024]
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features.
Pan X, Tao AM, Lu S, Ma M, Hannan SB, Slaugh R, Drewes Williams S, O'Grady L, Kanca O, Person R, et al. Am J Hum Genet. 2024 Apr 4; 111(4):742-760. Epub 2024 Mar 12.
Translocation (4;11)(p12;q23) with rearrangement of FRYL and MLL in therapy-related acute myeloid leukemia. [Cancer Genet Cytogenet. 2007]
Translocation (4;11)(p12;q23) with rearrangement of FRYL and MLL in therapy-related acute myeloid leukemia.
Sait SN, Claydon MA, Conroy JM, Nowak NJ, Barcos M, Baer MR. Cancer Genet Cytogenet. 2007 Sep; 177(2):143-6.
AF4p12, a human homologue to the furry gene of Drosophila, as a novel MLL fusion partner. [Cancer Res. 2005]
AF4p12, a human homologue to the furry gene of Drosophila, as a novel MLL fusion partner.
Hayette S, Cornillet-Lefebvre P, Tigaud I, Struski S, Forissier S, Berchet A, Doll D, Gillot L, Brahim W, Delabesse E, et al. Cancer Res. 2005 Aug 1; 65(15):6521-5.

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O94915 [Domain Mapping of Disease Mut...]
O94915
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
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reagents [ExactAntigen/Labome]
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ExactAntigen/Labome

RecName: Full=Protein furry homolog-like; AltName: Full=ALL1-fused gene from chr...
RecName: Full=Protein furry homolog-like; AltName: Full=ALL1-fused gene from chromosome 4p12 protein
gi|125991860|sp|O94915.2|FRYL_HUMAN

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