RecName: Full=Scavenger receptor class F member 2; AltName: Full=SRECR - Protein

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Identification of a novel variant of SCARF2 in a Jordanian family with a van den Ende-Gupta Syndrome and literature review. [Clin Dysmorphol. 2022]
Identification of a novel variant of SCARF2 in a Jordanian family with a van den Ende-Gupta Syndrome and literature review.
Odeh O, Barqawi T, Rashid H, Almashhdi S, Shboul M. Clin Dysmorphol. 2022 Jul 1; 31(3):157-161. Epub 2022 Mar 7.
Two novel variants in SCARF2 gene underlie van den Ende-Gupta syndrome. [Am J Med Genet A. 2022]
Two novel variants in SCARF2 gene underlie van den Ende-Gupta syndrome.
Karaer D, Karaer K. Am J Med Genet A. 2022 Jun; 188(6):1881-1884. Epub 2022 Feb 28.
Sclerocornea in a patient with van den Ende-Gupta syndrome homozygous for a SCARF2 microdeletion. [Am J Med Genet A. 2014]
Sclerocornea in a patient with van den Ende-Gupta syndrome homozygous for a SCARF2 microdeletion.
Migliavacca MP, Sobreira NL, Antonialli GP, Oliveira MM, Melaragno MI, Casteels I, de Ravel T, Brunoni D, Valle D, Perez AB. Am J Med Genet A. 2014 May; 164A(5):1170-4. Epub 2014 Jan 29.

RefSeq genomic sequence
See the genomic reference sequence for the SCARF2 gene (NG_031868.2).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the SCARF2 gene.

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Q96GP6 [Domain Mapping of Disease Mut...]
Q96GP6
Domain Mapping of Disease Mutations
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Protein