Homo sapiens cysteine rich with EGF like domains 1 (CRELD1), RefSeqGen - Nucleotide

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Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections. [Genet Med. 2024]
Biallelic CRELD1 variants cause a multisystem syndrome, including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.
Jeffries L, Mis EK, McWalter K, Donkervoort S, Brodsky NN, Carpier JM, Ji W, Ionita C, Roy B, Morrow JS, et al. Genet Med. 2024 Feb; 26(2):101023. Epub 2023 Nov 7.
CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome. [Hum Genet. 2023]
CRELD1 variants are associated with bicuspid aortic valve in Turner syndrome.
Pinnaro CT, Beck CB, Major HJ, Darbro BW. Hum Genet. 2023 Apr; 142(4):523-530. Epub 2023 Mar 16.
Associations of IL-17 and IL-17 receptor polymorphisms with Behçet's disease in Denizli Province of Turkey. [Immunol Res. 2023]
Associations of IL-17 and IL-17 receptor polymorphisms with Behçet's disease in Denizli Province of Turkey.
Arıkan S, Öztürk O, Duygulu Ş, Atalay EÖ, Atalay A. Immunol Res. 2023 Aug; 71(4):600-608. Epub 2023 Jan 26.

RefSeq alternative splicing
See 17 reference mRNA sequence splice variants for the CRELD1 gene.

Protein
Protein sequence from Nucleotide coding region
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RNA
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Order Prrt3 cDNA clone/Protein/Antibody/RNAi [OriGene]
Order Prrt3 cDNA clone/Protein/Antibody/RNAi
OriGene
Order Creld1 cDNA clone/Protein/Antibody/RNAi [OriGene]
Order Creld1 cDNA clone/Protein/Antibody/RNAi
OriGene
Order IL17RC cDNA clone/Protein/Antibody/RNAi [OriGene]
Order IL17RC cDNA clone/Protein/Antibody/RNAi
OriGene

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Nucleotide