Gene

rad21b

ID

ZDB-GENE-060503-223

Name

RAD21 cohesin complex component b

Symbol

rad21b Nomenclature History

Previous Names

si:ch211-246f9.1

Type

protein_coding_gene

Location

Chr: 19 Mapping Details/Browsers

Description

Predicted to have chromatin binding activity. Predicted to be involved in double-strand break repair; meiotic cell cycle; and sister chromatid cohesion. Predicted to localize to meiotic cohesin complex and nuclear cohesin complex. Human ortholog(s) of this gene implicated in Cornelia de Lange syndrome 4. Orthologous to human RAD21 (RAD21 cohesin complex component).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

No data available

Cross-Species Comparison

High Throughput Data

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Thisse Expression Data

No data available

Wild Type Expression Summary

Phenotype

All Phenotype Data: No data available
Cross-Species Comparison: Alliance

Phenotype Summary

Mutations

Mutants

Sequence Targeting Reagents

Human Disease

Associated With rad21b Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
Cornelia de Lange syndrome 4	Alliance	Cornelia de Lange syndrome 4	614701
		?Mungan syndrome	611376

Associated With rad21b Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Domain	IPR006909	Rad21/Rec8-like protein, C-terminal, eukaryotic
Domain	IPR006910	Rad21/Rec8-like protein, N-terminal
Family	IPR039781	Rad21/Rec8-like protein
Homologous_superfamily	IPR023093	ScpA-like, C-terminal
Homologous_superfamily	IPR036390	Winged helix DNA-binding domain superfamily