HR21spA, partial [Homo sapiens]

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Cornelia de Lange Syndrome Caused by an Intragenic Heterozygous Deletion in RAD21 Detected through Very-High-Resolution Chromosomal Microarray Analysis. [Genes (Basel). 2023]
Cornelia de Lange Syndrome Caused by an Intragenic Heterozygous Deletion in RAD21 Detected through Very-High-Resolution Chromosomal Microarray Analysis.
Abarca-Barriga HH, Punil Luciano R, Vásquez Sotomayor F. Genes (Basel). 2023 Dec 14; 14(12). Epub 2023 Dec 14.
RAD21 is the core subunit of the cohesin complex involved in directing genome organization. [Genome Biol. 2023]
RAD21 is the core subunit of the cohesin complex involved in directing genome organization.
Sun Y, Xu X, Zhao W, Zhang Y, Chen K, Li Y, Wang X, Zhang M, Xue B, Yu W, et al. Genome Biol. 2023 Jun 28; 24(1):155. Epub 2023 Jun 28.
Genetic variation as a long-distance modulator of RAD21 expression in humans. [Sci Rep. 2022]
Genetic variation as a long-distance modulator of RAD21 expression in humans.
Schierding W, Horsfield JA, O'Sullivan J. Sci Rep. 2022 Jul 29; 12(1):13035. Epub 2022 Jul 29.

RefSeq genomic sequence
See the genomic reference sequence for the RAD21 gene (NG_032862.1).
RefSeq protein
See the reference protein sequence for double-strand-break repair protein rad21 homolog (NP_006256.1).

Nucleotide
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Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
reagents [ExactAntigen/Labome]
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HR21spA, partial [Homo sapiens]
HR21spA, partial [Homo sapiens]
gi|1620398|emb|CAA66940.1|

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