Mm00517293_cn

• Gene Symbol: Atrx
• Assay Reference Genome Location: Chr.X:105845868 on build GRCm38
• Cytoband: XD

Target Gene Details

• Entrez Gene ID: 22589
• Gene Name: alpha thalassemia/mental retardation syndrome X-linked homolog (human)
• Gene Aliases: 4833408C14Rik, AI447451, ATR2, DXHXS6677E, HP1-BP38, Hp1bp2, Hp1bp38, MRXS3, RAD54L, Rad54, XH2, Xnp, ZNF-HX
• Location: Chr.X:105797615-105929408 on Build GRCm38
• Assay Gene Location: Within Exon 18

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
Atrx	NM_009530.2	18	5091	NP_033556.2
	AF026032.1	19	5058	AAC08741.1
	AK134024.1	10	1216	BAE21982.1
	AK161784.1	7	837	BAE36571.1

More Information

• Set Membership: Intragenic, Exonic

Panther Classification:

Molecular Function -

DNA-binding transcription factor, gene-specific transcriptional regulator

Gene Ontology Categories:

Process(es)

DNA repair
nucleosome assembly
DNA replication-independent nucleosome assembly
chromatin remodeling
transcription, DNA-templated
regulation of transcription, DNA-templated
cellular response to DNA damage stimulus
spermatogenesis
positive regulation of nuclear cell cycle DNA replication
chromatin modification
DNA damage response, signal transduction by p53 class mediator
forebrain development
replication fork processing
positive regulation of telomere maintenance
post-embryonic forelimb morphogenesis
multicellular organism growth
positive regulation of transcription from RNA polymerase II promoter
Sertoli cell development
seminiferous tubule development
cellular response to hydroxyurea
negative regulation of telomeric RNA transcription from RNA pol II promoter

Function(s)

nucleotide binding
DNA binding
chromatin binding
helicase activity
protein binding
ATP binding
zinc ion binding
DNA translocase activity
hydrolase activity
methylated histone binding
histone binding
metal ion binding
chromo shadow domain binding