Atrx (ATRX, chromatin remodeler) - Rat Genome Database

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Gene: Atrx (ATRX, chromatin remodeler) Mus musculus
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Symbol: Atrx
Name: ATRX, chromatin remodeler
RGD ID: 1553098
MGI Page MGI
Description: Enables chromatin binding activity and histone binding activity. Involved in several processes, including DNA damage response, signal transduction by p53 class mediator; cellular response to hydroxyurea; and positive regulation of DNA metabolic process. Acts upstream of or within several processes, including male gonad development; positive regulation of transcription by RNA polymerase II; and post-embryonic forelimb morphogenesis. Located in PML body and chromosome. Colocalizes with chromosome, telomeric region. Is expressed in several structures, including alimentary system; early embryo; egg cylinder; genitourinary system; and nervous system. Used to study alpha thalassemia-X-linked intellectual disability syndrome. Human ortholog(s) of this gene implicated in X-linked mental retardation-hypotonic facies syndrome-1; alpha thalassemia-X-linked intellectual disability syndrome; alpha-thalassemia myelodysplasia syndrome; high grade glioma; and lung small cell carcinoma. Orthologous to human ATRX (ATRX chromatin remodeler).
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: 4833408C14Rik; AI447451; alpha thalassemia/mental retardation syndrome (X-linked); alpha thalassemia/mental retardation syndrome X-linked; alpha thalassemia/mental retardation syndrome X-linked homolog; ATP-dependent helicase ATRX; ATR2; DXHXS6677; DXHXS6677E; heterochromatin protein 2; HP1 alpha-interacting protein; HP1-BP; HP1-BP38; Hp1b; Hp1bp2; Hp1bp38; MRXS3; Rad; Rad54; RAD54L; RIKEN cDNA 4833408C14 gene; transcriptional regulator ATRX; X; X-linked nuclear protein; XH2; Xnp; ZNF-HX
RGD Orthologs
Human
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Related Pseudogenes: Gm19194  
Latest Assembly: GRCm39 - Mouse Genome Assembly GRCm39
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X104,841,221 - 104,972,978 (-)NCBIGRCm39GRCm39mm39
GRCm39 EnsemblX104,841,221 - 104,973,009 (-)EnsemblGRCm39 Ensembl
GRCm38X105,797,615 - 105,929,372 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX105,797,615 - 105,929,403 (-)EnsemblGRCm38mm10GRCm38
MGSCv37X102,992,954 - 103,124,711 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36X102,002,872 - 102,132,061 (-)NCBIMGSCv36mm8
CeleraX92,651,743 - 92,783,324 (-)NCBICelera
Cytogenetic MapXDNCBI
cM MapX47.26NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Original Reference(s)
AtrxMousealpha thalassemia-X-linked intellectual disability syndrome  ISOATRX (Homo sapiens)9586027DNA:nonsense mutation:exon: c.109C>T (p.R37X)(human) RGD 
AtrxMousealpha thalassemia-X-linked intellectual disability syndrome  ISOATRX (Homo sapiens)9586030DNA:missense mutations:exons: c.6253C>T (p.R2085C), c.6254G>A (p.R2085H)(human) RGD 
AtrxMousealpha thalassemia-X-linked intellectual disability syndrome  ISOATRX (Homo sapiens)9586029DNA:missense mutations:exons: c.736C>T (p.R246C), c.736C>T (p.R246C)(human) RGD 
AtrxMousebrachydactyly  IMP 9586033 RGD 
AtrxMouseGastro-Enteropancreatic Neuroendocrine Tumor severityISOATRX (Homo sapiens)127285385 RGD 
AtrxMouseglioblastoma disease_progressionISOATRX (Homo sapiens)13442489 RGD 
AtrxMousehigh grade glioma  ISOATRX (Homo sapiens)11040587DNA:mutations: :multipleRGD 
AtrxMouseHuntington's disease  IEP 11040584 RGD 
AtrxMouseislet cell tumor disease_progressionISOATRX (Homo sapiens)9586032protein:decreased expression:pancreas:RGD 
AtrxMouselung adenocarcinoma disease_progressionISOATRX (Homo sapiens)127285382 RGD 
AtrxMouseLung Carcinoid Tumors disease_progressionISOATRX (Homo sapiens)127285379protein:decreased expression:nucleus and lungRGD 
AtrxMouselung small cell carcinoma disease_progressionISOATRX (Homo sapiens)127285383 RGD 
AtrxMouselung small cell carcinoma disease_progressionISOATRX (Homo sapiens)127285382 RGD 
AtrxMouselung squamous cell carcinoma severityISOATRX (Homo sapiens)127285382 RGD 
AtrxMousemalignant astrocytoma disease_progressionISOATRX (Homo sapiens)9586026 RGD 
AtrxMousemalignant astrocytoma severityISOATRX (Homo sapiens)11040585 RGD 
AtrxMousemelanoma disease_progressionISOATRX (Homo sapiens)9586028protein:decreased expression:skin:RGD 
AtrxMousesarcoma  ISOATRX (Homo sapiens)11536196protein:decreased expression: :RGD 
AtrxMousestomach cancer  IGISmad4 (Mus musculus)11354809 RGD 
AtrxMouseX-Linked Intellectual Developmental Disorders  ISOATRX (Homo sapiens)11040586DNA:missense mutation:cds:p.T1621M (human)RGD 
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AtrxMouseadrenocortical carcinoma  ISOATRX (Homo sapiens)8554872ClinVar more ...ClinVarPMID:15591283 more ...
AtrxMousealpha thalassemia-X-linked intellectual disability syndrome  ISOATRX (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10204841 more ...
AtrxMousealpha-thalassemia myelodysplasia syndrome  ISOATRX (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10398237 more ...
AtrxMouseanaplastic astrocytoma  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Astrocytoma and anaplasticClinVarPMID:18414213 more ...
AtrxMouseatypical teratoid rhabdoid tumor  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Atypical teratoid/rhabdoid tumorClinVarPMID:18414213 more ...
AtrxMouseautistic disorder  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: AutismClinVarPMID:21681106 and PMID:30208311
AtrxMouseautosomal hemophilia A  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: AUTOSOMAL HEMOPHILIA AClinVarPMID:31690835
AtrxMouseDevelopmental Disabilities  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Global developmental delayClinVarPMID:25741868 more ...
AtrxMouseDevelopmental Disease  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Developmental disorderClinVarPMID:25741868 more ...
AtrxMouseDwarfism  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Short statureClinVarPMID:25741868
AtrxMousefactor VIII deficiency  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Factor 8 deficiency and congenitalClinVarPMID:31690835
AtrxMousegenetic disease  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:10204841 more ...
AtrxMouseintellectual disability  ISOATRX (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10398237 more ...
AtrxMousemalignant astrocytoma  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Malignant astrocytomaClinVarPMID:18414213 more ...
AtrxMouseMenkes disease  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Menkes kinky-hair syndromeClinVarPMID:11241493 more ...
AtrxMousemicrocephaly  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: MicrocephalyClinVarPMID:25741868
AtrxMouseMuscle Hypotonia  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Neonatal hypotoniaClinVarPMID:10995512 more ...
AtrxMouseNervous System Malformations  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Abnormality of the nervous systemClinVarPMID:25741868
AtrxMouseNeurodevelopmental Disorders  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Neurodevelopmental disorderClinVarPMID:25741868
AtrxMouseschizophrenia  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: SchizophreniaClinVar 
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AtrxMouseadenoid cystic carcinoma  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:23685749
AtrxMousealpha thalassemia-X-linked intellectual disability syndrome  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
AtrxMousealpha-thalassemia myelodysplasia syndrome  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
AtrxMouseCraniofacial Abnormalities  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxMousecryptorchidism  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxMouseGrowth Disorders  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxMousehigh grade glioma  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:23583981 and PMID:24705251
AtrxMousemyelodysplastic syndrome  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19157545
AtrxMouseneuroblastoma  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:23334666 and PMID:26523776
AtrxMouseneuroendocrine tumor  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:21252315
AtrxMousepancreatic cancer  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:21252315
AtrxMousepenile disease  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxMousethoracic disease  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxMouseX-Linked Intellectual Developmental Disorders  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxMouseX-linked mental retardation-hypotonic facies syndrome-1  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
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AtrxMousealpha thalassemia-X-linked intellectual disability syndrome  IAGP 13592920OMIM:301040MouseDO 

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AtrxMouse(+)-dexrazoxane multiple interactionsEXP 6480464[Dexrazoxane co-treated with Idarubicin] results in increased expression of ATRX protein and Dexrazoxane inhibits the reaction [Idarubicin results in decreased expression of ATRX mRNA]CTDPMID:28973540
AtrxMouse(+)-pilocarpine increases expressionISOAtrx (Rattus norvegicus)6480464Pilocarpine results in increased expression of ATRX mRNACTDPMID:17971868
AtrxMouse(S)-nicotine increases expressionISOATRX (Homo sapiens)6480464Nicotine results in increased expression of ATRX mRNACTDPMID:16949557
AtrxMouse(S)-nicotine decreases expressionEXP 6480464Nicotine results in decreased expression of ATRX mRNACTDPMID:21955143
AtrxMouse1,2-dichloroethane decreases expressionEXP 6480464ethylene dichloride results in decreased expression of ATRX mRNACTDPMID:28960355
AtrxMouse1,2-dimethylhydrazine increases expressionEXP 64804641 and 2-Dimethylhydrazine results in increased expression of ATRX mRNACTDPMID:22206623
AtrxMouse1-[(4-chlorophenyl)-phenylmethyl]-4-methylpiperazine decreases expressionISOAtrx (Rattus norvegicus)6480464chlorcyclizine results in decreased expression of ATRX mRNACTDPMID:21058326
AtrxMouse17beta-estradiol decreases expressionISOAtrx (Rattus norvegicus)6480464Estradiol results in decreased expression of ATRX mRNACTDPMID:20068009
AtrxMouse17beta-estradiol increases expressionISOATRX (Homo sapiens)6480464Estradiol results in increased expression of ATRX mRNACTDPMID:36581016
AtrxMouse2,3',4,4',5-Pentachlorobiphenyl increases expressionEXP 64804642 more ...CTDPMID:31388691
AtrxMouse2,3,4,7,8-Pentachlorodibenzofuran decreases expressionISOAtrx (Rattus norvegicus)64804642 more ...CTDPMID:21724226
AtrxMouse2,3,7,8-tetrachlorodibenzodioxine affects expressionEXP 6480464Tetrachlorodibenzodioxin affects the expression of ATRX mRNACTDPMID:21570461
AtrxMouse2,3,7,8-tetrachlorodibenzodioxine affects expressionISOAtrx (Rattus norvegicus)6480464Tetrachlorodibenzodioxin affects the expression of ATRX mRNACTDPMID:34747641
AtrxMouse2,3,7,8-tetrachlorodibenzodioxine decreases expressionISOAtrx (Rattus norvegicus)6480464Tetrachlorodibenzodioxin results in decreased expression of ATRX mRNACTDPMID:32109520
AtrxMouse2,3,7,8-tetrachlorodibenzodioxine decreases expressionEXP 6480464Tetrachlorodibenzodioxin results in decreased expression of ATRX mRNACTDPMID:15034205
AtrxMouse2,3,7,8-Tetrachlorodibenzofuran decreases expressionISOAtrx (Rattus norvegicus)64804642 more ...CTDPMID:32109520
AtrxMouse2,6-dinitrotoluene affects expressionISOAtrx (Rattus norvegicus)64804642 and 6-dinitrotoluene affects the expression of ATRX mRNACTDPMID:21346803
AtrxMouse2-butoxyethanol decreases expressionEXP 6480464n-butoxyethanol results in decreased expression of ATRX mRNACTDPMID:19812364
AtrxMouse3,4-methylenedioxymethamphetamine decreases expressionEXP 6480464N-Methyl-3 and 4-methylenedioxyamphetamine results in decreased expression of ATRX mRNACTDPMID:26251327
AtrxMouse4-vinylcyclohexene dioxide affects expressionEXP 64804644-vinyl-1-cyclohexene dioxide affects the expression of ATRX mRNACTDPMID:20829426

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Biological Process
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AtrxMousecellular response to hydroxyurea involved_inIMP 2290270 PMID:24651726UniProtPMID:24651726
AtrxMousechromatin organization involved_inISSUniProtKB:P461002290270 UniProtGO_REF:0000024
AtrxMousechromatin organization involved_inISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousechromatin remodeling involved_inISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousechromatin remodeling involved_inISSUniProtKB:P461002290270 UniProtGO_REF:0000024
AtrxMousechromatin remodeling involved_inIBAPANTHER:PTN002923542 more ...2290270 GO_CentralGO_REF:0000033
AtrxMousechromosome organization involved in meiotic cell cycle acts_upstream_of_or_withinIMP 2290270 PMID:15242786MGIPMID:15242786
AtrxMouseDNA damage response, signal transduction by p53 class mediator involved_inIMP 2290270 PMID:24651726UniProtPMID:24651726
AtrxMouseDNA repair involved_inIEAUniProtKB-KW:KW-02342290270 UniProtGO_REF:0000043
AtrxMouseforebrain development acts_upstream_of_or_withinIMPMGI:35284802290270 PMID:15668733MGIPMID:15668733
AtrxMousemeiotic spindle organization acts_upstream_of_or_withinIMP 2290270 PMID:15242786MGIPMID:15242786
AtrxMousemulticellular organism growth acts_upstream_of_or_withinIMP 2290270 PMID:24386478MGIPMID:24386478
AtrxMousenegative regulation of maintenance of mitotic sister chromatid cohesion, telomeric involved_inISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousenegative regulation of maintenance of mitotic sister chromatid cohesion, telomeric involved_inIEAUniProtKB:P46100 and ensembl:ENSP000003624412290270 EnsemblGO_REF:0000107
AtrxMousenucleosome assembly involved_inISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousenucleosome assembly involved_inISSUniProtKB:P461002290270 UniProtGO_REF:0000024
AtrxMousepositive regulation of nuclear cell cycle DNA replication involved_inIMP 2290270 PMID:24651726UniProtPMID:24651726
AtrxMousepositive regulation of telomere maintenance involved_inIMP 2290270 PMID:20110566UniProtPMID:20110566
AtrxMousepositive regulation of transcription by RNA polymerase II involved_inISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousepositive regulation of transcription by RNA polymerase II acts_upstream_of_or_withinIGIMGI:880642290270 PMID:21427128MGIPMID:21427128
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Cellular Component
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AtrxMousechromosome, subtelomeric region located_inIEAUniProtKB:P46100 and ensembl:ENSP000003624412290270 EnsemblGO_REF:0000107
AtrxMousechromosome, subtelomeric region located_inISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousechromosome, telomeric region located_inIDA 2290270 PMID:20110566 more ...BHF-UCLPMID:20110566 more ...
AtrxMouseciliary basal body located_inISOATRX (Homo sapiens)9068941 HPAGO_REF:0000052
AtrxMousecilium located_inISOATRX (Homo sapiens)9068941 HPAGO_REF:0000052
AtrxMousecondensed chromosome, centromeric region located_inIDA 2290270 PMID:15242786MGIPMID:15242786
AtrxMousecytosol located_inISOATRX (Homo sapiens)9068941 HPAGO_REF:0000052
AtrxMouseheterochromatin located_inIDA 2290270 PMID:14519686 more ...MGIPMID:14519686 more ...
AtrxMousemicrotubule cytoskeleton located_inISOATRX (Homo sapiens)9068941 HPAGO_REF:0000052
AtrxMousenuclear body located_inISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousenuclear chromosome located_inIDA 2290270 PMID:11555636MGIPMID:11555636
AtrxMousenuclear speck located_inISOATRX (Homo sapiens)9068941 HPAGO_REF:0000052
AtrxMousenucleoplasm located_inISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousenucleus located_inIDA 2290270 PMID:17296936MGIPMID:17296936
AtrxMousenucleus is_active_inIBAPANTHER:PTN002923542 more ...2290270 GO_CentralGO_REF:0000033
AtrxMousepericentric heterochromatin located_inIDA 2290270 PMID:15242786 more ...BHF-UCLPMID:15242786 more ...
AtrxMousepericentric heterochromatin is_active_inIBAPANTHER:PTN002923542 more ...2290270 GO_CentralGO_REF:0000033
AtrxMousePML body located_inIDA 2290270 PMID:23444137BHF-UCLPMID:23444137
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Molecular Function
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AtrxMouseATP binding enablesIEAUniProtKB-KW:KW-00672290270 UniProtGO_REF:0000043
AtrxMouseATP hydrolysis activity enablesIEARHEA:130652290270 RHEAGO_REF:0000116
AtrxMousechromatin binding enablesISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousechromatin binding enablesIDA 2290270 PMID:15522233MGIPMID:15522233
AtrxMousechromatin DNA binding enablesIBAPANTHER:PTN002923542 and FB:FBgn00265732290270 GO_CentralGO_REF:0000033
AtrxMousechromo shadow domain binding enablesIEAUniProtKB:P46100 and ensembl:ENSP000003624412290270 EnsemblGO_REF:0000107
AtrxMousechromo shadow domain binding enablesISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMouseDNA binding enablesIEAUniProtKB-KW:KW-02382290270 UniProtGO_REF:0000043
AtrxMouseDNA translocase activity enablesIEAUniProtKB:P46100 and ensembl:ENSP000003624412290270 EnsemblGO_REF:0000107
AtrxMouseDNA translocase activity enablesISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousedouble-stranded DNA helicase activity enablesIEAEC:3.6.4.122290270 UniProtGO_REF:0000003
AtrxMouseforked DNA-dependent helicase activity enablesIEAEC:3.6.4.122290270 UniProtGO_REF:0000003
AtrxMousefour-way junction helicase activity enablesIEAEC:3.6.4.122290270 UniProtGO_REF:0000003
AtrxMousehistone binding enablesIPIUniProtKB:P842432290270 PMID:20110566BHF-UCLPMID:20110566
AtrxMousehistone binding enablesISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousehistone binding enablesIDA 2290270 PMID:20211137UniProtPMID:20211137
AtrxMousehistone H3K9me2/3 reader activity enablesISOATRX (Homo sapiens)9068941 PMID:21421568UniProtPMID:21421568
AtrxMousemethylated histone binding enablesIEAUniProtKB:P46100 and ensembl:ENSP000003624412290270 EnsemblGO_REF:0000107
AtrxMousemethylated histone binding enablesISOUniProtKB:P461002290270 GO_CentralGO_REF:0000119
AtrxMousemethylated histone binding enablesIBAPANTHER:PTN002923542 more ...2290270 GO_CentralGO_REF:0000033
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AtrxMouseabnormal behavior  IAGP 5509061 MGIPMID:16628246
AtrxMouseabnormal developmental patterning  IEA 5509061 MGI 
AtrxMouseabnormal ectoplacental cone morphology  IAGP 5509061 MGIPMID:16628246
AtrxMouseabnormal eye electrophysiology  IAGP 5509061 MGIPMID:19088125
AtrxMouseabnormal heart morphology  IEA 5509061 MGI 
AtrxMouseabnormal imprinting  IAGP 5509061 MGIPMID:16628246
AtrxMouseabnormal reproductive system physiology  IAGP 5509061 MGIPMID:16628246
AtrxMouseabnormal retina ganglion layer morphology  IAGP 5509061 MGIPMID:19088125
AtrxMouseabnormal retina horizontal cell morphology  IAGP 5509061 MGIPMID:19088125
AtrxMouseabnormal retina inner nuclear layer morphology  IAGP 5509061 MGIPMID:19088125
AtrxMouseabnormal retina morphology  IAGP 5509061 MGIPMID:19088125
AtrxMouseabnormal suckling behavior  IAGP 5509061 MGIPMID:15668733
AtrxMouseabnormal trophectoderm morphology  IAGP 5509061 MGIPMID:16628246
AtrxMouseabsent dentate gyrus  IAGP 5509061 MGIPMID:15668733
AtrxMouseabsent gastric milk in neonates  IAGP 5509061 MGIPMID:15668733
AtrxMousedecreased amacrine cell number  IAGP 5509061 MGIPMID:19088125
AtrxMousedecreased birth body size  IAGP 5509061 MGIPMID:15668733
AtrxMousedecreased body weight  IAGP 5509061 MGIPMID:20865721
AtrxMousedecreased cell proliferation  IAGP 5509061 MGIPMID:16628246
AtrxMousedecreased embryo size  IAGP 5509061 MGIPMID:16628246
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Reference Title
Reference Citation
1. The alternative lengthening of telomere phenotype is significantly associated with loss of ATRX expression in high-grade pediatric and adult astrocytomas: a multi-institutional study of 214 astrocytomas. Abedalthagafi M, etal., Mod Pathol. 2013 Nov;26(11):1425-32. doi: 10.1038/modpathol.2013.90. Epub 2013 Jun 14.
2. Alpha-thalassemia intellectual disability: variable phenotypic expression among males with a recurrent nonsense mutation - c.109C>T (p.R37X). Basehore MJ, etal., Clin Genet. 2014 May 7. doi: 10.1111/cge.12420.
3. Novel ATRX gene damaging missense mutation c.6740A>C segregates with profound to severe intellectual deficiency without alpha thalassaemia. Bouazzi H, etal., Indian J Med Res. 2016 Jan;143(1):43-8. doi: 10.4103/0971-5916.178589.
4. Expression and prognostic impact of alpha thalassemia/mental retardation X-linked and death domain-associated protein in human lung cancer. Buentzel J, etal., Medicine (Baltimore). 2019 Aug;98(31):e16712. doi: 10.1097/MD.0000000000016712.
5. ATRX mRNA expression combined with IDH1/2 mutational status and Ki-67 expression refines the molecular classification of astrocytic tumors: evidence from the whole transcriptome sequencing of 169 samples samples. Cai J, etal., Oncotarget. 2014 May 15;5(9):2551-61.
6. Immunohistochemical Analysis of ATRX, IDH1 and p53 in Glioblastoma and Their Correlations with Patient Survival. Chaurasia A, etal., J Korean Med Sci. 2016 Aug;31(8):1208-14. doi: 10.3346/jkms.2016.31.8.1208. Epub 2016 May 30.
7. Genomic alterations of plasma cell-free DNAs in small cell lung cancer and their clinical relevance. Du M, etal., Lung Cancer. 2018 Jun;120:113-121. doi: 10.1016/j.lungcan.2018.04.008. Epub 2018 Apr 12.
8. A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy. Guerrini R, etal., Ann Neurol. 2000 Jan;47(1):117-21.
9. Whole-exome sequencing identifies ATRX mutation as a key molecular determinant in lower-grade glioma. Kannan K, etal., Oncotarget. 2012 Oct;3(10):1194-203.
10. Telomere length abnormalities and telomerase RNA component expression in gastroenteropancreatic neuroendocrine tumors. Kim HS, etal., Anticancer Res. 2015 Jun;35(6):3501-10.
11. Mutations of codon 2085 in the helicase domain of ATRX are recurrent and cause ATRX syndrome. Lacoste C, etal., Clin Genet. 2013 Dec 1. doi: 10.1111/cge.12319.
12. A possible involvement of TIF1 alpha and TIF1 beta in the epigenetic control of transcription by nuclear receptors. Le Douarin B, etal., EMBO J 1996 Dec 2;15(23):6701-15.
13. ATRX induction by mutant huntingtin via Cdx2 modulates heterochromatin condensation and pathology in Huntington's disease. Lee J, etal., Cell Death Differ. 2012 Jul;19(7):1109-16. doi: 10.1038/cdd.2011.196. Epub 2012 Jan 13.
14. Comprehensive screening of alternative lengthening of telomeres phenotype and loss of ATRX expression in sarcomas. Liau JY, etal., Mod Pathol. 2015 Dec;28(12):1545-54. doi: 10.1038/modpathol.2015.114. Epub 2015 Oct 2.
15. [Mutation analysis for a Chinese family featuring X-linked alpha thalassemia/mental retardation syndrome]. Lin SB, etal., Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2013 Dec;30(6):654-8. doi: 10.3760/cma.j.issn.1003-9406.2013.06.004.
16. Loss of DAXX and ATRX are associated with chromosome instability and reduced survival of patients with pancreatic neuroendocrine tumors. Marinoni I, etal., Gastroenterology. 2014 Feb;146(2):453-60.e5. doi: 10.1053/j.gastro.2013.10.020. Epub 2013 Oct 19.
17. MGDs mouse GO annotations MGD data from the GO Consortium
18. MGD IEA MGD IEA
19. Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Okazaki Y, etal., Nature. 2002 Dec 5;420(6915):563-73.
20. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
1 to 20 of 30 rows
1 to 10 of 12 rows
PMID:7874112   PMID:8162050   PMID:8889548   PMID:8921375   PMID:9545503   PMID:9607915   PMID:9736627   PMID:10349636   PMID:10570185   PMID:10757799   PMID:10922068   PMID:11042159  
PMID:11076861   PMID:11217851   PMID:11544199   PMID:11823444   PMID:12520002   PMID:12904583   PMID:14519686   PMID:14610273   PMID:14654002   PMID:14681479   PMID:15242786   PMID:15252119  
PMID:15522233   PMID:15668733   PMID:16141072   PMID:16141073   PMID:16452087   PMID:16602821   PMID:16628246   PMID:16935872   PMID:17296936   PMID:17503331   PMID:18227278   PMID:18287559  
PMID:18366812   PMID:18799693   PMID:18842153   PMID:19005673   PMID:19020049   PMID:19088125   PMID:19538749   PMID:19571810   PMID:19615340   PMID:19774083   PMID:20110566   PMID:20150414  
PMID:20159591   PMID:20211137   PMID:20548051   PMID:20651253   PMID:20865721   PMID:20885787   PMID:21029860   PMID:21057507   PMID:21209221   PMID:21267068   PMID:21317870   PMID:21357745  
PMID:21421568   PMID:21427128   PMID:21672208   PMID:21677750   PMID:21873635   PMID:22500635   PMID:22573614   PMID:22918800   PMID:23114596   PMID:23284920   PMID:23362347   PMID:23444137  
PMID:23563309   PMID:23754746   PMID:24270455   PMID:24386478   PMID:24651726   PMID:24946904   PMID:24990380   PMID:25395668   PMID:25417162   PMID:25452430   PMID:25865896   PMID:26012739  
PMID:26159997   PMID:26206133   PMID:26340527   PMID:26477563   PMID:26496610   PMID:26836306   PMID:26936505   PMID:27171262   PMID:27863708   PMID:28093507   PMID:28173139   PMID:28186538  
PMID:28341773   PMID:28358373   PMID:28666128   PMID:28684628   PMID:29095838   PMID:29535300   PMID:29719265   PMID:29785027   PMID:29883366   PMID:30126901   PMID:30186101   PMID:30204892  
PMID:30231518   PMID:30335163   PMID:30510993   PMID:31029404   PMID:31040226   PMID:31671722   PMID:31713968   PMID:31895940   PMID:32376827   PMID:32610139   PMID:32821827   PMID:33197500  
1 to 10 of 12 rows



Atrx
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39X104,841,221 - 104,972,978 (-)NCBIGRCm39GRCm39mm39
GRCm39 EnsemblX104,841,221 - 104,973,009 (-)EnsemblGRCm39 Ensembl
GRCm38X105,797,615 - 105,929,372 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 EnsemblX105,797,615 - 105,929,403 (-)EnsemblGRCm38mm10GRCm38
MGSCv37X102,992,954 - 103,124,711 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36X102,002,872 - 102,132,061 (-)NCBIMGSCv36mm8
CeleraX92,651,743 - 92,783,324 (-)NCBICelera
Cytogenetic MapXDNCBI
cM MapX47.26NCBI
ATRX
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X77,504,880 - 77,786,216 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 EnsemblX77,504,880 - 77,786,233 (-)EnsemblGRCh38hg38GRCh38
GRCh37X76,760,358 - 77,041,702 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X76,647,012 - 76,928,375 (-)NCBINCBI36Build 36hg18NCBI36
CeleraX77,001,253 - 77,282,613 (-)NCBICelera
Cytogenetic MapXq21.1NCBI
HuRefX70,349,443 - 70,629,029 (-)NCBIHuRef
CHM1_1X76,653,073 - 76,934,420 (-)NCBICHM1_1
T2T-CHM13v2.0X75,942,420 - 76,223,770 (-)NCBIT2T-CHM13v2.0
Atrx
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8X74,916,548 - 75,062,880 (-)NCBIGRCr8
mRatBN7.2X70,850,981 - 70,997,330 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 EnsemblX70,850,981 - 70,997,330 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_UtxX72,359,919 - 72,506,253 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0X75,860,229 - 76,006,565 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0X73,423,392 - 73,569,729 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0X76,820,110 - 76,979,155 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 EnsemblX76,820,329 - 76,979,115 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 EnsemblX76,692,970 - 76,708,878 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0X77,469,497 - 77,515,204 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Rnor_5.0X55,943,493 - 56,101,756 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4X93,903,794 - 94,051,337 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1X94,034,366 - 94,057,029 (-)NCBI
CeleraX72,164,814 - 72,309,854 (-)NCBICelera
Cytogenetic MapXq22NCBI
Atrx
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955557947,167 - 1,252,724 (-)EnsemblChiLan1.0
ChiLan1.0NW_004955557947,368 - 1,252,701 (-)NCBIChiLan1.0ChiLan1.0
ATRX
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2X77,081,989 - 77,368,610 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1X77,085,587 - 77,372,212 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0X66,682,968 - 66,969,421 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1X76,795,574 - 77,083,486 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 EnsemblX76,795,574 - 77,083,486 (-)Ensemblpanpan1.1panPan2
ATRX
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1X59,772,067 - 60,107,016 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 EnsemblX59,774,585 - 60,106,980 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_TashaX50,787,446 - 51,120,278 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0X61,011,471 - 61,270,437 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 EnsemblX61,011,677 - 61,270,443 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1X58,719,357 - 59,051,934 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0X60,325,606 - 60,661,270 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0X59,917,163 - 60,249,816 (-)NCBIUU_Cfam_GSD_1.0
Atrx
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2X42,229,198 - 42,451,804 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049366832,495,959 - 2,718,620 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049366832,496,307 - 2,718,539 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ATRX
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 EnsemblX61,584,848 - 61,872,287 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1X61,584,028 - 61,872,341 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2X70,390,618 - 70,509,341 (-)NCBISscrofa10.2Sscrofa10.2susScr3
ATRX
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1X66,449,830 - 66,737,220 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 EnsemblX66,448,449 - 66,737,164 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366606714,772,636 - 15,066,083 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

.

.
Variants in Atrx
2075 total Variants

Predicted Target Of
Summary Value
Count of predictions:2965
Count of miRNA genes:945
Interacting mature miRNAs:1320
Transcripts:ENSMUST00000101305, ENSMUST00000113573, ENSMUST00000123174, ENSMUST00000126345, ENSMUST00000127221, ENSMUST00000128968, ENSMUST00000130980, ENSMUST00000133543, ENSMUST00000134381, ENSMUST00000134507, ENSMUST00000137453, ENSMUST00000138765, ENSMUST00000141609, ENSMUST00000142235, ENSMUST00000143361, ENSMUST00000146193, ENSMUST00000150914, ENSMUST00000154866, ENSMUST00000155445
Prediction methods:Miranda, Pita, Rnahybrid, Targetscan
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


1 to 10 of 10 rows
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD ID
Symbol
Name
LOD
P Value
Trait
Sub Trait
Chr
Start
Stop
Species
4141630Gct6_mgranulosa cell tumorigenesis 6 (mouse)Not determined47179121129764756Mouse
13208552Wght12_mweight 12 (mouse)X94043606149782996Mouse
4141803Lmr30_mleishmaniasis resistance 30 (mouse)Not determined85062606119062720Mouse
13208556Lgth14_mbody length 14 (mouse)X94043606149782996Mouse
13824980Ferq1_mgenetic fertility QTL 1 (mouse)X54045360148782996Mouse
11075102Modc2_mmodifier of Odc2 (mouse)X80189914114190059Mouse
1357500Mdmsc6_mmodifier of muscularity 6 (mouse)Not determinedX75306671109306758Mouse
1357823Spha3_msperm head anomaly 3 (mouse)Not determinedX102055848162758941Mouse
1357433Dbts2_mdiabetes 2 (mouse)Not determinedX7226295150107038Mouse
4141665Mhysq2_mmale hybrid sterility QTL 2 (mouse)Not determined71453852139203212Mouse

1 to 10 of 10 rows
DXMit213  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X105,864,610 - 105,864,721UniSTSGRCm38
MGSCv37X103,059,949 - 103,060,060UniSTSGRCm37
CeleraX92,718,708 - 92,718,837UniSTS
Cytogenetic MapXDUniSTS
cM MapX44.4UniSTS
Whitehead GeneticX31.7UniSTS
Whitehead/MRC_RHX1159.63UniSTS
Whitehead_YACX UniSTS
AI447451  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X105,797,898 - 105,797,998UniSTSGRCm38
MGSCv37X102,993,237 - 102,993,337UniSTSGRCm37
CeleraX92,652,026 - 92,652,126UniSTS
Cytogenetic MapXDUniSTS
cM MapX43.8UniSTS
Whitehead/MRC_RHX1159.73UniSTS
RH126483  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X105,873,855 - 105,874,067UniSTSGRCm38
MGSCv37X103,069,194 - 103,069,406UniSTSGRCm37
CeleraX92,728,028 - 92,728,240UniSTS
Cytogenetic MapXDUniSTS
cM MapX42.0UniSTS
Whitehead/MRC_RHX1159.73UniSTS
MARC_6759-6760:992007400:1  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X105,855,973 - 105,856,579UniSTSGRCm38
MGSCv37X103,051,312 - 103,051,918UniSTSGRCm37
CeleraX92,710,046 - 92,710,652UniSTS
Cytogenetic MapXDUniSTS
cM MapX43.8UniSTS
GDB:596212  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X105,830,948 - 105,832,496UniSTSGRCm38
MGSCv37X103,026,287 - 103,027,835UniSTSGRCm37
CeleraX92,685,056 - 92,686,604UniSTS
Cytogenetic MapXDUniSTS
cM MapX43.8UniSTS
GDB:596250  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38X105,801,406 - 105,802,803UniSTSGRCm38
MGSCv37X102,996,745 - 102,998,142UniSTSGRCm37
CeleraX92,655,534 - 92,656,931UniSTS
Cytogenetic MapXDUniSTS
cM MapX43.8UniSTS
Atrx  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic MapXDUniSTS
cM MapX47.26UniSTS






1 to 19 of 19 rows
RefSeq Transcripts NM_009530 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AF026032 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK014663 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK032955 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK080333 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK082779 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK088095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK134024 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK135019 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK138878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK161784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK164705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK172134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL670660 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL671893 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH466564 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  EF410140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L34362 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X99643 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 19 of 19 rows

Ensembl Acc Id: ENSMUST00000101305   ⟹   ENSMUSP00000098863
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,925,561 - 104,972,183 (-)Ensembl
GRCm38.p6 EnsemblX105,881,955 - 105,928,577 (-)Ensembl
Ensembl Acc Id: ENSMUST00000113573   ⟹   ENSMUSP00000109203
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,841,221 - 104,973,009 (-)Ensembl
GRCm38.p6 EnsemblX105,797,615 - 105,929,403 (-)Ensembl
Ensembl Acc Id: ENSMUST00000123174
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,895,043 - 104,918,870 (-)Ensembl
GRCm38.p6 EnsemblX105,851,437 - 105,875,264 (-)Ensembl
Ensembl Acc Id: ENSMUST00000126345
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,943,512 - 104,972,952 (-)Ensembl
GRCm38.p6 EnsemblX105,899,906 - 105,929,346 (-)Ensembl
Ensembl Acc Id: ENSMUST00000127221   ⟹   ENSMUSP00000143664
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,861,676 - 104,869,731 (-)Ensembl
GRCm38.p6 EnsemblX105,818,070 - 105,826,125 (-)Ensembl
Ensembl Acc Id: ENSMUST00000128968   ⟹   ENSMUSP00000121416
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,918,736 - 104,972,972 (-)Ensembl
GRCm38.p6 EnsemblX105,875,130 - 105,929,366 (-)Ensembl
Ensembl Acc Id: ENSMUST00000130980   ⟹   ENSMUSP00000117528
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,931,387 - 104,973,003 (-)Ensembl
GRCm38.p6 EnsemblX105,887,781 - 105,929,397 (-)Ensembl
Ensembl Acc Id: ENSMUST00000133543
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,921,975 - 104,923,993 (-)Ensembl
GRCm38.p6 EnsemblX105,878,369 - 105,880,387 (-)Ensembl
Ensembl Acc Id: ENSMUST00000134381   ⟹   ENSMUSP00000122875
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,920,846 - 104,972,973 (-)Ensembl
GRCm38.p6 EnsemblX105,877,240 - 105,929,367 (-)Ensembl
Ensembl Acc Id: ENSMUST00000134507   ⟹   ENSMUSP00000123085
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,920,566 - 104,972,956 (-)Ensembl
GRCm38.p6 EnsemblX105,876,960 - 105,929,350 (-)Ensembl
Ensembl Acc Id: ENSMUST00000137453   ⟹   ENSMUSP00000120246
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,927,962 - 104,972,909 (-)Ensembl
GRCm38.p6 EnsemblX105,884,356 - 105,929,303 (-)Ensembl
Ensembl Acc Id: ENSMUST00000138765
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,845,356 - 104,847,404 (-)Ensembl
GRCm38.p6 EnsemblX105,801,750 - 105,803,798 (-)Ensembl
Ensembl Acc Id: ENSMUST00000141609
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,861,702 - 104,873,252 (-)Ensembl
GRCm38.p6 EnsemblX105,818,096 - 105,829,646 (-)Ensembl
Ensembl Acc Id: ENSMUST00000142235
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,881,985 - 104,890,563 (-)Ensembl
GRCm38.p6 EnsemblX105,838,379 - 105,846,957 (-)Ensembl
Ensembl Acc Id: ENSMUST00000143361
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,844,023 - 104,845,656 (-)Ensembl
GRCm38.p6 EnsemblX105,800,417 - 105,802,050 (-)Ensembl
Ensembl Acc Id: ENSMUST00000146193
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,890,343 - 104,895,132 (-)Ensembl
GRCm38.p6 EnsemblX105,846,737 - 105,851,526 (-)Ensembl
Ensembl Acc Id: ENSMUST00000150914   ⟹   ENSMUSP00000122034
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,920,566 - 104,972,976 (-)Ensembl
GRCm38.p6 EnsemblX105,876,960 - 105,929,370 (-)Ensembl
Ensembl Acc Id: ENSMUST00000154866   ⟹   ENSMUSP00000121291
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,921,047 - 104,972,965 (-)Ensembl
GRCm38.p6 EnsemblX105,877,441 - 105,929,359 (-)Ensembl
Ensembl Acc Id: ENSMUST00000155445
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,881,630 - 104,890,379 (-)Ensembl
GRCm38.p6 EnsemblX105,838,024 - 105,846,773 (-)Ensembl
Ensembl Acc Id: ENSMUST00000196998
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,889,990 - 104,895,420 (-)Ensembl
GRCm38.p6 EnsemblX105,846,384 - 105,851,814 (-)Ensembl
Ensembl Acc Id: ENSMUST00000197302   ⟹   ENSMUSP00000143163
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,900,209 - 104,931,429 (-)Ensembl
GRCm38.p6 EnsemblX105,856,603 - 105,887,823 (-)Ensembl
Ensembl Acc Id: ENSMUST00000198209   ⟹   ENSMUSP00000142726
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,895,609 - 104,919,201 (-)Ensembl
GRCm38.p6 EnsemblX105,852,003 - 105,875,595 (-)Ensembl
Ensembl Acc Id: ENSMUST00000198441   ⟹   ENSMUSP00000143565
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,921,995 - 104,972,844 (-)Ensembl
GRCm38.p6 EnsemblX105,878,389 - 105,929,238 (-)Ensembl
Ensembl Acc Id: ENSMUST00000198448   ⟹   ENSMUSP00000143090
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,920,114 - 104,972,948 (-)Ensembl
GRCm38.p6 EnsemblX105,876,508 - 105,929,342 (-)Ensembl
Ensembl Acc Id: ENSMUST00000198567   ⟹   ENSMUSP00000143007
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,869,750 - 104,881,877 (-)Ensembl
GRCm38.p6 EnsemblX105,826,144 - 105,838,271 (-)Ensembl
Ensembl Acc Id: ENSMUST00000199233   ⟹   ENSMUSP00000143015
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,921,086 - 104,972,953 (-)Ensembl
GRCm38.p6 EnsemblX105,877,480 - 105,929,347 (-)Ensembl
Ensembl Acc Id: ENSMUST00000200471   ⟹   ENSMUSP00000143280
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 EnsemblX104,909,152 - 104,918,911 (-)Ensembl
GRCm38.p6 EnsemblX105,865,546 - 105,875,305 (-)Ensembl
RefSeq Acc Id: NM_009530   ⟹   NP_033556
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39X104,841,221 - 104,972,978 (-)NCBI
GRCm38X105,797,615 - 105,929,372 (-)NCBI
MGSCv37X102,992,954 - 103,124,711 (-)RGD
CeleraX92,651,743 - 92,783,324 (-)RGD
cM MapX ENTREZGENE
Sequence:
1 to 5 of 18 rows
1 to 5 of 18 rows
RefSeq Acc Id: NP_033556   ⟸   NM_009530
- UniProtKB: A2ADH4 (UniProtKB/Swiss-Prot),   Q61687 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSMUSP00000143007   ⟸   ENSMUST00000198567
Ensembl Acc Id: ENSMUSP00000122034   ⟸   ENSMUST00000150914
Ensembl Acc Id: ENSMUSP00000142726   ⟸   ENSMUST00000198209
Ensembl Acc Id: ENSMUSP00000143565   ⟸   ENSMUST00000198441
Name Modeler Protein Id AA Range Protein Structure
AF-Q61687-F1-model_v2 AlphaFold Q61687 1-2476 view protein structure

RGD ID:6845509
Promoter ID:MM_KWN:61495
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Brain,   Lung
Transcripts:OTTMUST00000044144
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X102,996,796 - 102,998,332 (-)MPROMDB
RGD ID:6845510
Promoter ID:MM_KWN:61496
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Brain
Transcripts:OTTMUST00000044143
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X102,998,631 - 102,999,131 (-)MPROMDB
RGD ID:6845505
Promoter ID:MM_KWN:61498
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Kidney
Transcripts:OTTMUST00000044142
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X103,021,811 - 103,022,311 (-)MPROMDB
RGD ID:6845506
Promoter ID:MM_KWN:61499
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Liver
Transcripts:OTTMUST00000044141
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X103,024,801 - 103,025,301 (-)MPROMDB
RGD ID:6845507
Promoter ID:MM_KWN:61503
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Liver
Transcripts:OTTMUST00000044138,   UC009UBC.1
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X103,046,306 - 103,046,806 (-)MPROMDB
RGD ID:6845504
Promoter ID:MM_KWN:61505
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:Brain,   Kidney,   Liver,   Lung
Transcripts:OTTMUST00000044137
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X103,070,696 - 103,071,597 (-)MPROMDB
RGD ID:6845511
Promoter ID:MM_KWN:61506
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:BoneMarrow_0Hour,   Brain,   Liver,   MEF_B6
Transcripts:OTTMUST00000058534
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X103,075,246 - 103,076,427 (-)MPROMDB
RGD ID:6845503
Promoter ID:MM_KWN:61510
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:3T3L1_Day0,   3T3L1_Day1,   3T3L1_Day2,   3T3L1_Day3,   3T3L1_Day4,   BoneMarrow_0Hour,   BoneMarrow_2Hour,   BoneMarrow_4Hour,   Brain,   ES_Cell,   Kidney,   Liver,   Lung,   MEF_B4,   MEF_B6,   Spleen
Transcripts:ENSMUST00000087810,   ENSMUST00000101305,   ENSMUST00000113573,   ENSMUST00000113574,   OTTMUST00000044145,   OTTMUST00000058530,   OTTMUST00000058531,   OTTMUST00000058532,   OTTMUST00000058533,   UC009UBE.1,   UC009UBF.1
Position:
Mouse AssemblyChrPosition (strand)Source
MGSCv36X103,124,136 - 103,124,932 (-)MPROMDB
RGD ID:13681172
Promoter ID:EPDNEW_M24736
Type:multiple initiation site
Name:Atrx_2
Description:Mus musculus ATRX, chromatin remodeler , mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_M24737  
Experiment Methods:Single-end sequencing.
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm38X105,928,577 - 105,928,637EPDNEW
RGD ID:13681176
Promoter ID:EPDNEW_M24737
Type:initiation region
Name:Atrx_1
Description:Mus musculus ATRX, chromatin remodeler , mRNA.
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_M24736  
Experiment Methods:Single-end sequencing.
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm38X105,929,350 - 105,929,410EPDNEW


1 to 40 of 60 rows
Database
Acc Id
Source(s)
Ensembl Genes ENSMUSG00000031229 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENSMUST00000113573 ENTREZGENE
  ENSMUST00000113573.8 UniProtKB/Swiss-Prot
Gene3D-CATH 3.30.40.10 UniProtKB/Swiss-Prot
  3.40.50.10810 UniProtKB/Swiss-Prot
  3.40.50.300 UniProtKB/Swiss-Prot
  SWI2/SNF2 ATPases, N-terminal domain UniProtKB/Swiss-Prot
InterPro ADD UniProtKB/Swiss-Prot
  ADD_ATRX UniProtKB/Swiss-Prot
  ATRX_domain-containing UniProtKB/Swiss-Prot
  Helicase_ATP-bd UniProtKB/Swiss-Prot
  Helicase_C UniProtKB/Swiss-Prot
  P-loop_NTPase UniProtKB/Swiss-Prot
  SNF2-like_sf UniProtKB/Swiss-Prot
  SNF2/RAD54-like_C UniProtKB/Swiss-Prot
  SNF2_N UniProtKB/Swiss-Prot
  Znf_FYVE_PHD UniProtKB/Swiss-Prot
  Znf_RING/FYVE/PHD UniProtKB/Swiss-Prot
KEGG Report mmu:22589 UniProtKB/Swiss-Prot
MGD MGI:103067 ENTREZGENE
NCBI Gene 22589 ENTREZGENE
PANTHER TRANSCRIPTIONAL REGULATOR ATRX UniProtKB/Swiss-Prot
  TRANSCRIPTIONAL REGULATOR ATRX UniProtKB/Swiss-Prot
Pfam ADD_ATRX UniProtKB/Swiss-Prot
  Helicase_C UniProtKB/Swiss-Prot
  SNF2_N UniProtKB/Swiss-Prot
PhenoGen Atrx PhenoGen
PROSITE ADD UniProtKB/Swiss-Prot
  HELICASE_ATP_BIND_1 UniProtKB/Swiss-Prot
  HELICASE_CTER UniProtKB/Swiss-Prot
SMART DEXDc UniProtKB/Swiss-Prot
  HELICc UniProtKB/Swiss-Prot
Superfamily-SCOP SSF52540 UniProtKB/Swiss-Prot
  SSF57903 UniProtKB/Swiss-Prot
UniProt A0A0G2JED2_MOUSE UniProtKB/TrEMBL
  A0A0G2JF35_MOUSE UniProtKB/TrEMBL
  A0A0G2JF42_MOUSE UniProtKB/TrEMBL
  A0A0G2JFA5_MOUSE UniProtKB/TrEMBL
  A0A0G2JFG6_MOUSE UniProtKB/TrEMBL
  A0A0G2JFR8_MOUSE UniProtKB/TrEMBL
1 to 40 of 60 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-03-21 Atrx  ATRX, chromatin remodeler    alpha thalassemia/mental retardation syndrome X-linked  Symbol and/or name change 5135510 APPROVED
2016-04-05 Atrx  alpha thalassemia/mental retardation syndrome X-linked  4833408C14Rik  RIKEN cDNA 4833408C14 gene  Data merged from RGD:1608143 737654 PROVISIONAL
2015-12-22 Atrx  alpha thalassemia/mental retardation syndrome X-linked    alpha thalassemia/mental retardation syndrome X-linked homolog (human)  Symbol and/or name change 5135510 APPROVED