Atrx alpha thalassemia/mental retardation syndrome X-linked homolog (human) (22589) | Macrophage Network Portal

Summary

	Symbol	Product	Feature Type	Strand	Chr
22589	Atrx	alpha thalassemia/mental retardation syndrome X-linked homolog (human)	protein-coding		X

Synonyms

Synonyms
4833408C14Rik \| AI447451 \| ATR2 \| DXHXS6677E \| HP1-BP38 \| Hp1bp2 \| Hp1bp38 \| MRXS3 \| RAD54L \| Rad54 \| XH2 \| Xnp \| ZNF-HX

DB XRef

Ensembl	MGI	VEGA
ENSMUSG00000031229	MGI:103067	OTTMUSG00000018268

GO Terms

GO ID	Category	Definition	Evidence
GO:0000166 GO:0000228 GO:0000792 GO:0003676 GO:0003677 GO:0003682 GO:0004386 GO:0005515 GO:0005524 GO:0005634 GO:0006281 GO:0006974 GO:0008270 GO:0016787 GO:0030900 GO:0046872 GO:0070087	Function Component Process	nucleotide binding nuclear chromosome heterochromatin nucleic acid binding DNA binding chromatin binding helicase activity protein binding ATP binding nucleus DNA repair cellular response to DNA damage stimulus zinc ion binding hydrolase activity forebrain development metal ion binding chromo shadow domain binding	IEA IDA IPI IMP ISO

Regulatory Modules

	Motif 1	Motif 2	Residual

Regulation

Displaying 1 - 1 of 1

Regulator Locus	Interaction	Weight

String Network

Entrez ID	STRINGS Network
STRING

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