PREDICTED: Homo sapiens heparan sulfate proteoglycan 2 (HSPG2), transc - Nucleotide

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Dyssegmental dysplasia Rolland-Desbuquois type is caused by pathogenic variants in HSPG2 - a founder haplotype shared in five patients. [J Hum Genet. 2024]
Dyssegmental dysplasia Rolland-Desbuquois type is caused by pathogenic variants in HSPG2 - a founder haplotype shared in five patients.
Farshadyeganeh P, Yamada T, Ohashi H, Nishimura G, Fujita H, Oishi Y, Nunode M, Ishikawa S, Murotsuki J, Yamashita Y, et al. J Hum Genet. 2024 Jun; 69(6):235-244. Epub 2024 Feb 29.
Proteomic analysis of SARS-CoV-2 particles unveils a key role of G3BP proteins in viral assembly. [Nat Commun. 2024]
Proteomic analysis of SARS-CoV-2 particles unveils a key role of G3BP proteins in viral assembly.
Murigneux E, Softic L, Aubé C, Grandi C, Judith D, Bruce J, Le Gall M, Guillonneau F, Schmitt A, Parissi V, et al. Nat Commun. 2024 Jan 20; 15(1):640. Epub 2024 Jan 20.
Perlecan (HSPG2) promotes structural, contractile, and metabolic development of human cardiomyocytes. [Cell Rep. 2024]
Perlecan (HSPG2) promotes structural, contractile, and metabolic development of human cardiomyocytes.
Johnson BB, Cosson MV, Tsansizi LI, Holmes TL, Gilmore T, Hampton K, Song OR, Vo NTN, Nasir A, Chabronova A, et al. Cell Rep. 2024 Jan 23; 43(1):113668. Epub 2024 Jan 9.

RefSeq protein product
See the reference protein sequence for basement membrane-specific heparan sulfate proteoglycan core protein isoform X4 (XP_016856609.1).

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PREDICTED: Homo sapiens heparan sulfate proteoglycan 2 (HSPG2), transcript varia...
PREDICTED: Homo sapiens heparan sulfate proteoglycan 2 (HSPG2), transcript variant X4, mRNA
gi|1034558038|ref|XM_017001120.1|

Nucleotide

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Nucleotide