RecName: Full=F-box/LRR-repeat protein 3; AltName: Full=F-box and leuc - Protein

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Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature. [Hum Mol Genet. 2019]
Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature.
Ansar M, Paracha SA, Serretti A, Sarwar MT, Khan J, Ranza E, Falconnet E, Iwaszkiewicz J, Shah SF, Qaisar AA, et al. Hum Mol Genet. 2019 Mar 15; 28(6):972-979.
Highly Efficient Genome Editing via CRISPR/Cas9 to Create Clock Gene Knockout Cells. [J Biol Rhythms. 2015]
Highly Efficient Genome Editing via CRISPR/Cas9 to Create Clock Gene Knockout Cells.
Korge S, Grudziecki A, Kramer A. J Biol Rhythms. 2015 Oct; 30(5):389-95. Epub 2015 Aug 4.
Severe mental retardation, short stature, facial anomalies, joint laxity, and dislocations in two sisters: previously undescribed MCA/MR syndrome. [Am J Med Genet. 2001]
Severe mental retardation, short stature, facial anomalies, joint laxity, and dislocations in two sisters: previously undescribed MCA/MR syndrome.
Mégarbané A, Cormier-Daire V. Am J Med Genet. 2001 Aug 1; 102(2):153-6.

RefSeq protein isoforms
See 4 reference sequence protein isoforms for the FBXL3 gene.

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Q9UKT7 [Domain Mapping of Disease Mut...]
Q9UKT7
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=F-box/LRR-repeat protein 3; AltName: Full=F-box and leucine-rich r...
RecName: Full=F-box/LRR-repeat protein 3; AltName: Full=F-box and leucine-rich repeat protein 3A; AltName: Full=F-box/LRR-repeat protein 3A
gi|37537866|sp|Q9UKT7.1|FBXL3_HUMAN

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