RecName: Full=Double-strand-break repair protein rad21 homolog; Short= - Protein

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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 protein
See the reference protein sequence for double-strand-break repair protein rad21 homolog (NP_006256.1).

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O60216 [Domain Mapping of Disease Mut...]
O60216
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
reagent reviews [ExactAntigen/Labome]
reagent reviews
ExactAntigen/Labome

RecName: Full=Double-strand-break repair protein rad21 homolog; Short=hHR21; Alt...
RecName: Full=Double-strand-break repair protein rad21 homolog; Short=hHR21; AltName: Full=Nuclear matrix protein 1; Short=NXP-1; AltName: Full=SCC1 homolog; Contains: RecName: Full=64-kDa C-terminal product; AltName: Full=64-kDa carboxy-terminal product; AltName: Full=65-kDa carboxy-terminal product
gi|25091097|sp|O60216.2|RAD21_HUMAN

Protein
NMU neuromedin U [Homo sapiens]
NMU neuromedin U [Homo sapiens]
Gene ID:10874

Gene
"Coprococcus comes" (11662)
Nucleotide
MTERF1 mitochondrial transcription termination factor 1 [Homo sapiens]
MTERF1 mitochondrial transcription termination factor 1 [Homo sapiens]
Gene ID:7978

Gene
7978[uid] AND (alive[prop]) (1)
Gene

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Protein