Atrx (ATRX, chromatin remodeler) - Rat Genome Database

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Gene: Atrx (ATRX, chromatin remodeler) Rattus norvegicus
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Symbol: Atrx
Name: ATRX, chromatin remodeler
RGD ID: 619795
Description: Predicted to enable several functions, including DNA translocase activity; chromo shadow domain binding activity; and methylated histone binding activity. Predicted to be involved in several processes, including DNA damage response, signal transduction by p53 class mediator; chromatin remodeling; and positive regulation of nucleobase-containing compound metabolic process. Predicted to act upstream of or within several processes, including male gonad development; meiotic spindle organization; and post-embryonic forelimb morphogenesis. Predicted to be located in several cellular components, including chromosomal region; ciliary basal body; and nuclear lumen. 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); INTERACTS WITH (+)-pilocarpine; 1-[(4-chlorophenyl)-phenylmethyl]-4-methylpiperazine; 17beta-estradiol.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: alpha thalassemia/mental retardation syndrome X-linked; alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae); alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S.cerevisiae); alpha thalassemia/mental retardation syndrome X-linked homolog; alpha thalassemia/mental retardation syndrome X-linked homolog (human); ATP-dependent helicase ATRX; helicase II; LOC103690008; pABP-2; transcriptional regulator ATRX; transcriptional regulator ATRX-like; X-linked nuclear protein; Xnp
RGD Orthologs
Human
Mouse
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Latest Assembly: GRCr8 - GRCr8 Assembly
Position:
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
JBrowse: View Region in Genome Browser (JBrowse)
Model


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Original Reference(s)
AtrxRatalpha thalassemia-X-linked intellectual disability syndrome  ISOATRX (Homo sapiens)9586027DNA:nonsense mutation:exon: c.109C>T (p.R37X)(human) RGD 
AtrxRatalpha 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 
AtrxRatalpha 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 
AtrxRatbrachydactyly  ISOAtrx (Mus musculus)9586033 RGD 
AtrxRatGastro-Enteropancreatic Neuroendocrine Tumor severityISOATRX (Homo sapiens)127285385 RGD 
AtrxRatglioblastoma disease_progressionISOATRX (Homo sapiens)13442489 RGD 
AtrxRathigh grade glioma  ISOATRX (Homo sapiens)11040587DNA:mutations: :multipleRGD 
AtrxRatHuntington's disease  ISOAtrx (Mus musculus)11040584 RGD 
AtrxRatislet cell tumor disease_progressionISOATRX (Homo sapiens)9586032protein:decreased expression:pancreas:RGD 
AtrxRatlung adenocarcinoma disease_progressionISOATRX (Homo sapiens)127285382 RGD 
AtrxRatLung Carcinoid Tumors disease_progressionISOATRX (Homo sapiens)127285379protein:decreased expression:nucleus and lungRGD 
AtrxRatlung small cell carcinoma disease_progressionISOATRX (Homo sapiens)127285383 RGD 
AtrxRatlung small cell carcinoma disease_progressionISOATRX (Homo sapiens)127285382 RGD 
AtrxRatlung squamous cell carcinoma severityISOATRX (Homo sapiens)127285382 RGD 
AtrxRatmalignant astrocytoma disease_progressionISOATRX (Homo sapiens)9586026 RGD 
AtrxRatmalignant astrocytoma severityISOATRX (Homo sapiens)11040585 RGD 
AtrxRatmelanoma disease_progressionISOATRX (Homo sapiens)9586028protein:decreased expression:skin:RGD 
AtrxRatsarcoma  ISOATRX (Homo sapiens)11536196protein:decreased expression: :RGD 
AtrxRatstomach cancer  ISOAtrx (Mus musculus)11354809 RGD 
AtrxRatX-Linked Intellectual Developmental Disorders  ISOATRX (Homo sapiens)11040586DNA:missense mutation:cds:p.T1621M (human)RGD 
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AtrxRatadrenocortical carcinoma  ISOATRX (Homo sapiens)8554872ClinVar more ...ClinVarPMID:15591283 more ...
AtrxRatalpha thalassemia-X-linked intellectual disability syndrome  ISOATRX (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10204841 more ...
AtrxRatalpha-thalassemia myelodysplasia syndrome  ISOATRX (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10398237 more ...
AtrxRatanaplastic astrocytoma  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Astrocytoma and anaplasticClinVarPMID:18414213 more ...
AtrxRatatypical teratoid rhabdoid tumor  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Atypical teratoid/rhabdoid tumorClinVarPMID:18414213 more ...
AtrxRatautistic disorder  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: AutismClinVarPMID:21681106 and PMID:30208311
AtrxRatautosomal hemophilia A  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: AUTOSOMAL HEMOPHILIA AClinVarPMID:31690835
AtrxRatDevelopmental Disabilities  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Global developmental delayClinVarPMID:25741868 more ...
AtrxRatDevelopmental Disease  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Developmental disorderClinVarPMID:25741868 more ...
AtrxRatDwarfism  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Short statureClinVarPMID:25741868
AtrxRatfactor VIII deficiency  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Factor 8 deficiency and congenitalClinVarPMID:31690835
AtrxRatgenetic disease  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Inborn genetic diseasesClinVarPMID:10204841 more ...
AtrxRatintellectual disability  ISOATRX (Homo sapiens)8554872ClinVar more ...ClinVarPMID:10398237 more ...
AtrxRatmalignant astrocytoma  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Malignant astrocytomaClinVarPMID:18414213 more ...
AtrxRatMenkes disease  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Menkes kinky-hair syndromeClinVarPMID:11241493 more ...
AtrxRatmicrocephaly  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: MicrocephalyClinVarPMID:25741868
AtrxRatMuscle Hypotonia  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Neonatal hypotoniaClinVarPMID:10995512 more ...
AtrxRatNervous System Malformations  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Abnormality of the nervous systemClinVarPMID:25741868
AtrxRatNeurodevelopmental Disorders  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: Neurodevelopmental disorderClinVarPMID:25741868
AtrxRatschizophrenia  ISOATRX (Homo sapiens)8554872ClinVar Annotator: match by term: SchizophreniaClinVar 
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AtrxRatadenoid cystic carcinoma  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:23685749
AtrxRatalpha thalassemia-X-linked intellectual disability syndrome  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
AtrxRatalpha-thalassemia myelodysplasia syndrome  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
AtrxRatCraniofacial Abnormalities  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxRatcryptorchidism  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxRatGrowth Disorders  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxRathigh grade glioma  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:23583981 and PMID:24705251
AtrxRatmyelodysplastic syndrome  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19157545
AtrxRatneuroblastoma  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:23334666 and PMID:26523776
AtrxRatneuroendocrine tumor  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:21252315
AtrxRatpancreatic cancer  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:21252315
AtrxRatpenile disease  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxRatthoracic disease  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxRatX-Linked Intellectual Developmental Disorders  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTDPMID:19291773
AtrxRatX-linked mental retardation-hypotonic facies syndrome-1  ISOATRX (Homo sapiens)11554173CTD Direct Evidence: marker/mechanismCTD 
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AtrxRatalpha thalassemia-X-linked intellectual disability syndrome  ISSAtrx (Mus musculus)13592920OMIM:301040MouseDO 

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AtrxRat(+)-dexrazoxane multiple interactionsISOAtrx (Mus musculus)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
AtrxRat(+)-pilocarpine increases expressionEXP 6480464Pilocarpine results in increased expression of ATRX mRNACTDPMID:17971868
AtrxRat(S)-nicotine increases expressionISOATRX (Homo sapiens)6480464Nicotine results in increased expression of ATRX mRNACTDPMID:16949557
AtrxRat(S)-nicotine decreases expressionISOAtrx (Mus musculus)6480464Nicotine results in decreased expression of ATRX mRNACTDPMID:21955143
AtrxRat1,2-dichloroethane decreases expressionISOAtrx (Mus musculus)6480464ethylene dichloride results in decreased expression of ATRX mRNACTDPMID:28960355
AtrxRat1,2-dimethylhydrazine increases expressionISOAtrx (Mus musculus)64804641 and 2-Dimethylhydrazine results in increased expression of ATRX mRNACTDPMID:22206623
AtrxRat1-[(4-chlorophenyl)-phenylmethyl]-4-methylpiperazine decreases expressionEXP 6480464chlorcyclizine results in decreased expression of ATRX mRNACTDPMID:21058326
AtrxRat17beta-estradiol decreases expressionEXP 6480464Estradiol results in decreased expression of ATRX mRNACTDPMID:20068009
AtrxRat17beta-estradiol increases expressionISOATRX (Homo sapiens)6480464Estradiol results in increased expression of ATRX mRNACTDPMID:36581016
AtrxRat2,3',4,4',5-Pentachlorobiphenyl increases expressionISOAtrx (Mus musculus)64804642 more ...CTDPMID:31388691
AtrxRat2,3,4,7,8-Pentachlorodibenzofuran decreases expressionEXP 64804642 more ...CTDPMID:21724226
AtrxRat2,3,7,8-tetrachlorodibenzodioxine affects expressionISOAtrx (Mus musculus)6480464Tetrachlorodibenzodioxin affects the expression of ATRX mRNACTDPMID:21570461
AtrxRat2,3,7,8-tetrachlorodibenzodioxine affects expressionEXP 6480464Tetrachlorodibenzodioxin affects the expression of ATRX mRNACTDPMID:34747641
AtrxRat2,3,7,8-tetrachlorodibenzodioxine decreases expressionEXP 6480464Tetrachlorodibenzodioxin results in decreased expression of ATRX mRNACTDPMID:32109520
AtrxRat2,3,7,8-tetrachlorodibenzodioxine decreases expressionISOAtrx (Mus musculus)6480464Tetrachlorodibenzodioxin results in decreased expression of ATRX mRNACTDPMID:15034205
AtrxRat2,3,7,8-Tetrachlorodibenzofuran decreases expressionEXP 64804642 more ...CTDPMID:32109520
AtrxRat2,6-dinitrotoluene affects expressionEXP 64804642 and 6-dinitrotoluene affects the expression of ATRX mRNACTDPMID:21346803
AtrxRat2-butoxyethanol decreases expressionISOAtrx (Mus musculus)6480464n-butoxyethanol results in decreased expression of ATRX mRNACTDPMID:19812364
AtrxRat3,4-methylenedioxymethamphetamine decreases expressionISOAtrx (Mus musculus)6480464N-Methyl-3 and 4-methylenedioxyamphetamine results in decreased expression of ATRX mRNACTDPMID:26251327
AtrxRat4-vinylcyclohexene dioxide affects expressionISOAtrx (Mus musculus)64804644-vinyl-1-cyclohexene dioxide affects the expression of ATRX mRNACTDPMID:20829426

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Biological Process
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AtrxRatbiological_process  ND 15984075/2021: no relevant rat dataRGD 
AtrxRatcellular response to hydroxyurea involved_inIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatcellular response to hydroxyurea involved_inISSUniProtKB:Q616871600115GO_REF:0000024UniProtGO_REF:0000024
AtrxRatcellular response to hydroxyurea involved_inISOAtrx (Mus musculus)1624291 PMID:24651726RGDPMID:24651726
AtrxRatchromatin organization involved_inISOATRX (Homo sapiens)1624291 PMID:22391447RGDPMID:22391447
AtrxRatchromatin organization involved_inIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatchromatin organization involved_inIEAUniProtKB-KW:KW-01561600115GO_REF:0000043UniProtGO_REF:0000043
AtrxRatchromatin organization involved_inISSUniProtKB:P461001600115GO_REF:0000024UniProtGO_REF:0000024
AtrxRatchromatin remodeling involved_inISSUniProtKB:P461001600115GO_REF:0000024UniProtGO_REF:0000024
AtrxRatchromatin remodeling involved_inISOATRX (Homo sapiens)1624291 PMID:10742099 more ...RGDPMID:10742099 more ...
AtrxRatchromatin remodeling involved_inIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatchromosome organization involved in meiotic cell cycle acts_upstream_of_or_withinISOAtrx (Mus musculus)1624291 PMID:15242786RGDPMID:15242786
AtrxRatchromosome organization involved in meiotic cell cycle acts_upstream_of_or_withinIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatDNA damage response involved_inIEAUniProtKB-KW:KW-02271600115GO_REF:0000043UniProtGO_REF:0000043
AtrxRatDNA damage response, signal transduction by p53 class mediator involved_inISSUniProtKB:Q616871600115GO_REF:0000024UniProtGO_REF:0000024
AtrxRatDNA damage response, signal transduction by p53 class mediator involved_inISOAtrx (Mus musculus)1624291 PMID:24651726RGDPMID:24651726
AtrxRatDNA damage response, signal transduction by p53 class mediator involved_inIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatDNA repair involved_inIEAUniProtKB-KW:KW-02341600115GO_REF:0000043UniProtGO_REF:0000043
AtrxRatforebrain development acts_upstream_of_or_withinIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatforebrain development acts_upstream_of_or_withinISOAtrx (Mus musculus)1624291MGI:3528480 PMID:15668733RGDPMID:15668733
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Cellular Component
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AtrxRatchromosome located_inIEAUniProtKB-KW:KW-01581600115GO_REF:0000043UniProtGO_REF:0000043
AtrxRatchromosome, subtelomeric region located_inIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatchromosome, subtelomeric region located_inISOATRX (Homo sapiens)1624291 PMID:26055325RGDPMID:26055325
AtrxRatchromosome, telomeric region located_inISSUniProtKB:Q616871600115GO_REF:0000024UniProtGO_REF:0000024
AtrxRatchromosome, telomeric region located_inIEAUniProtKB-KW:KW-07791600115GO_REF:0000043UniProtGO_REF:0000043
AtrxRatchromosome, telomeric region located_inISOAtrx (Mus musculus)1624291 PMID:20110566 more ...RGDPMID:20110566 more ...
AtrxRatchromosome, telomeric region located_inIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatchromosome, telomeric region located_inIEAUniProtKB-SubCell:SL-02761600115GO_REF:0000044UniProtGO_REF:0000044
AtrxRatciliary basal body located_inISOATRX (Homo sapiens)1624291 RGDGO_REF:0000052
AtrxRatcilium located_inISOATRX (Homo sapiens)1624291 RGDGO_REF:0000052
AtrxRatcondensed chromosome, centromeric region located_inIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatcondensed chromosome, centromeric region located_inISOAtrx (Mus musculus)1624291 PMID:15242786RGDPMID:15242786
AtrxRatcytosol located_inISOATRX (Homo sapiens)1624291 RGDGO_REF:0000052
AtrxRatheterochromatin located_inISOAtrx (Mus musculus)1624291 PMID:14519686 more ...RGDPMID:14519686 more ...
AtrxRatheterochromatin located_inIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatmicrotubule cytoskeleton located_inISOATRX (Homo sapiens)1624291 RGDGO_REF:0000052
AtrxRatnuclear body located_inISOATRX (Homo sapiens) more ...1624291 RGDGO_REF:0000052
AtrxRatnuclear body located_inIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatnuclear body located_inIEAUniProtKB:A4LAA3 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatnuclear chromosome located_inIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
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Molecular Function
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AtrxRatATP binding enablesIEAUniProtKB-KW:KW-00671600115GO_REF:0000043UniProtGO_REF:0000043
AtrxRatATP binding enablesIEAInterPro:IPR0003301600115GO_REF:0000002InterProGO_REF:0000002
AtrxRatATP hydrolysis activity enablesIEARHEA:130651600115GO_REF:0000116RHEAGO_REF:0000116
AtrxRatchromatin binding enablesIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatchromatin binding enablesISOAtrx (Mus musculus)1624291 PMID:15522233RGDPMID:15522233
AtrxRatchromatin binding enablesISOATRX (Homo sapiens)1624291 PMID:27029610RGDPMID:27029610
AtrxRatchromatin binding enablesISSUniProtKB:P461001600115GO_REF:0000024UniProtGO_REF:0000024
AtrxRatchromatin binding enablesIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatchromo shadow domain binding enablesIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatchromo shadow domain binding enablesISOATRX (Homo sapiens)1624291UniProtKB:P45973 and PMID:15882967RGDPMID:15882967
AtrxRatDNA binding enablesIEAUniProtKB-KW:KW-02381600115GO_REF:0000043UniProtGO_REF:0000043
AtrxRatDNA translocase activity enablesIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRatDNA translocase activity enablesISOATRX (Homo sapiens)1624291 PMID:12953102RGDPMID:12953102
AtrxRathelicase activity enablesIEAUniProtKB-KW:KW-03471600115GO_REF:0000043UniProtGO_REF:0000043
AtrxRathistone binding enablesISSUniProtKB:Q616871600115GO_REF:0000024UniProtGO_REF:0000024
AtrxRathistone binding enablesIEAUniProtKB:Q61687 and ensembl:ENSMUSP000001092031600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRathistone binding enablesIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
AtrxRathistone binding enablesISOAtrx (Mus musculus)1624291UniProtKB:P84243 more ...RGDPMID:20110566 and PMID:20211137
AtrxRathistone binding enablesISOATRX (Homo sapiens)1624291 PMID:20211137 and PMID:22391447RGDPMID:20211137 and PMID:22391447
AtrxRathistone H3K9me2/3 reader activity enablesIEAUniProtKB:P46100 and ensembl:ENSP000003624411600115GO_REF:0000107EnsemblGO_REF:0000107
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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. Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium. Gaudet P, etal., Brief Bioinform. 2011 Sep;12(5):449-62. doi: 10.1093/bib/bbr042. Epub 2011 Aug 27.
9. A nonsense mutation of the ATRX gene causing mild mental retardation and epilepsy. Guerrini R, etal., Ann Neurol. 2000 Jan;47(1):117-21.
10. 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.
11. Telomere length abnormalities and telomerase RNA component expression in gastroenteropancreatic neuroendocrine tumors. Kim HS, etal., Anticancer Res. 2015 Jun;35(6):3501-10.
12. 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.
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. Rat ISS GO annotations from MGI mouse gene data--August 2006 MGD data from the GO Consortium
18. Electronic Transfer of LocusLink and RefSeq Data NCBI rat LocusLink and RefSeq merged data July 26, 2002
19. Molecular cloning and characterization of annexin V-binding proteins with highly hydrophilic peptide structure. Ohsawa K, etal., J Neurochem 1996 Jul;67(1):89-97.
20. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
1 to 20 of 32 rows
PMID:11555636   PMID:12477932   PMID:12953102   PMID:14519686   PMID:15242786   PMID:15252119   PMID:15522233   PMID:15668733   PMID:15882967   PMID:17296936   PMID:20110566   PMID:20211137  
PMID:20651253   PMID:21421568   PMID:21427128   PMID:22391447   PMID:23444137   PMID:24386478   PMID:24651726   PMID:26055325   PMID:26159997   PMID:26373281   PMID:27029610   PMID:37320994  



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
(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
(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
(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
236 total Variants

Predicted Target Of
Summary Value
Count of predictions:120
Count of miRNA genes:99
Interacting mature miRNAs:100
Transcripts:ENSRNOT00000042751, ENSRNOT00000045534
Prediction methods:Microtar, Miranda, Pita, Rnahybrid
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.


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
61430Cia18Collagen induced arthritis QTL 183.1joint integrity trait (VT:0010548)joint inflammation composite score (CMO:0000919)X14843113120568734Rat
61431Cia19Collagen induced arthritis QTL 194.4joint integrity trait (VT:0010548)joint inflammation composite score (CMO:0000919)X65612192120568734Rat
738035Stresp1Stress response QTL 14.960.000011stress-related behavior trait (VT:0010451)defensive burying - copingX41304447112935181Rat
1598837Memor13Memory QTL 133.2exploratory behavior trait (VT:0010471)difference between time of physical contact/close proximity of test subject and social stimulus during sample phase and test phase (CMO:0002678)X41052407146860749Rat

DXMgh10  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2X70,871,973 - 70,872,106 (+)MAPPERmRatBN7.2
Rnor_6.0X76,841,244 - 76,841,376NCBIRnor6.0
Rnor_5.0X55,964,627 - 55,964,759UniSTSRnor5.0
RGSC_v3.4X93,924,589 - 93,924,722RGDRGSC3.4
RGSC_v3.4X93,924,590 - 93,924,722UniSTSRGSC3.4
RGSC_v3.1X93,998,022 - 93,998,155RGD
CeleraX72,185,808 - 72,185,937UniSTS
Cytogenetic MapXq31UniSTS
RH142511  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2X70,899,773 - 70,899,880 (+)MAPPERmRatBN7.2
Rnor_6.0X76,869,042 - 76,869,148NCBIRnor6.0
Rnor_5.0X55,992,425 - 55,992,531UniSTSRnor5.0
RGSC_v3.4X93,952,390 - 93,952,496UniSTSRGSC3.4
CeleraX72,213,604 - 72,213,710UniSTS
Cytogenetic MapXq31UniSTS
MARC_6759-6760:992007400:1  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2X70,912,436 - 70,912,996 (+)MAPPERmRatBN7.2
Rnor_6.0X76,881,270 - 76,881,829NCBIRnor6.0
Rnor_6.0X76,666,051 - 76,666,610NCBIRnor6.0
Rnor_5.0X56,004,653 - 56,005,212UniSTSRnor5.0
Rnor_5.0X77,472,343 - 77,472,902UniSTSRnor5.0
RGSC_v3.4X93,965,086 - 93,965,645UniSTSRGSC3.4
CeleraX72,226,236 - 72,226,795UniSTS
Cytogenetic MapXq31UniSTS
GDB:596250  
Rat AssemblyChrPosition (strand)SourceJBrowse
mRatBN7.2X70,855,127 - 70,856,601 (+)MAPPERmRatBN7.2
Rnor_6.0X76,824,257 - 76,825,730NCBIRnor6.0
Rnor_5.0X55,947,640 - 55,949,113UniSTSRnor5.0
RGSC_v3.4X93,907,744 - 93,909,217UniSTSRGSC3.4
CeleraX72,168,961 - 72,170,434UniSTS
Cytogenetic MapXq31UniSTS




alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
nervous system
renal system
reproductive system
respiratory system
15 11 53 135 114 109 67 31 67 12 257 119 103 48 72 42


1 to 30 of 43 rows
RefSeq Transcripts NM_001105757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588264 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588269 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588270 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017588274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017602341 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099458 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099466 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099468 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099469 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099471 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099473 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_039099475 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
1 to 30 of 43 rows

Ensembl Acc Id: ENSRNOT00000045534   ⟹   ENSRNOP00000051120
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.0 EnsemblX76,692,970 - 76,708,878 (-)Ensembl
Ensembl Acc Id: ENSRNOT00000078997   ⟹   ENSRNOP00000071468
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 EnsemblX70,939,675 - 70,996,592 (-)Ensembl
Rnor_6.0 EnsemblX76,908,189 - 76,924,362 (-)Ensembl
Ensembl Acc Id: ENSRNOT00000086752
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.0 EnsemblX76,857,656 - 76,865,244 (-)Ensembl
Ensembl Acc Id: ENSRNOT00000087977   ⟹   ENSRNOP00000070457
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 EnsemblX70,850,981 - 70,956,139 (-)Ensembl
Rnor_6.0 EnsemblX76,823,010 - 76,925,195 (-)Ensembl
Ensembl Acc Id: ENSRNOT00000088571
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.0 EnsemblX76,890,272 - 76,899,366 (-)Ensembl
Ensembl Acc Id: ENSRNOT00000091284
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 EnsemblX70,850,981 - 70,997,330 (-)Ensembl
Rnor_6.0 EnsemblX76,820,329 - 76,979,115 (-)Ensembl
Ensembl Acc Id: ENSRNOT00000095781   ⟹   ENSRNOP00000087702
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
mRatBN7.2 EnsemblX70,850,981 - 70,997,330 (-)Ensembl
RefSeq Acc Id: NM_001105757   ⟹   NP_001099227
RefSeq Status: VALIDATED
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,880 (-)NCBI
mRatBN7.2X70,850,981 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099458   ⟹   XP_038955386
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,162 (-)NCBI
mRatBN7.2X70,850,981 - 70,996,607 (-)NCBI
RefSeq Acc Id: XM_039099459   ⟹   XP_038955387
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,157 (-)NCBI
mRatBN7.2X70,853,881 - 70,996,607 (-)NCBI
RefSeq Acc Id: XM_039099460   ⟹   XP_038955388
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,157 (-)NCBI
mRatBN7.2X70,853,881 - 70,996,607 (-)NCBI
RefSeq Acc Id: XM_039099461   ⟹   XP_038955389
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,157 (-)NCBI
mRatBN7.2X70,853,881 - 70,996,607 (-)NCBI
RefSeq Acc Id: XM_039099462   ⟹   XP_038955390
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099464   ⟹   XP_038955392
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099465   ⟹   XP_038955393
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099466   ⟹   XP_038955394
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099467   ⟹   XP_038955395
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099468   ⟹   XP_038955396
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099469   ⟹   XP_038955397
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099470   ⟹   XP_038955398
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099471   ⟹   XP_038955399
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,298 (-)NCBI
RefSeq Acc Id: XM_039099472   ⟹   XP_038955400
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099473   ⟹   XP_038955401
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
mRatBN7.2X70,853,881 - 70,997,330 (-)NCBI
RefSeq Acc Id: XM_039099475   ⟹   XP_038955403
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,946,604 - 75,062,162 (-)NCBI
mRatBN7.2X70,883,232 - 70,996,607 (-)NCBI
RefSeq Acc Id: XM_063279780   ⟹   XP_063135850
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,877 (-)NCBI
RefSeq Acc Id: XM_063279782   ⟹   XP_063135852
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,172 (-)NCBI
RefSeq Acc Id: XM_063279783   ⟹   XP_063135853
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,165 (-)NCBI
RefSeq Acc Id: XM_063279784   ⟹   XP_063135854
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
RefSeq Acc Id: XM_063279786   ⟹   XP_063135856
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,876 (-)NCBI
RefSeq Acc Id: XM_063279787   ⟹   XP_063135857
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,175 (-)NCBI
RefSeq Acc Id: XM_063279788   ⟹   XP_063135858
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 75,062,165 (-)NCBI
RefSeq Acc Id: XM_063279789   ⟹   XP_063135859
Type: CODING
Position:
Rat AssemblyChrPosition (strand)Source
GRCr8X74,916,548 - 74,982,507 (-)NCBI
1 to 30 of 32 rows
Protein RefSeqs NP_001099227 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955386 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955387 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955388 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955389 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955390 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955392 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955393 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955394 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955395 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955396 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955397 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955398 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955399 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955400 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955401 (Get FASTA)   NCBI Sequence Viewer  
  XP_038955403 (Get FASTA)   NCBI Sequence Viewer  
  XP_063135850 (Get FASTA)   NCBI Sequence Viewer  
  XP_063135852 (Get FASTA)   NCBI Sequence Viewer  
  XP_063135853 (Get FASTA)   NCBI Sequence Viewer  
  XP_063135854 (Get FASTA)   NCBI Sequence Viewer  
  XP_063135856 (Get FASTA)   NCBI Sequence Viewer  
  XP_063135857 (Get FASTA)   NCBI Sequence Viewer  
  XP_063135858 (Get FASTA)   NCBI Sequence Viewer  
  XP_063135859 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAI69005 (Get FASTA)   NCBI Sequence Viewer  
  BAA10936 (Get FASTA)   NCBI Sequence Viewer  
  EDM07145 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSRNOP00000070457
  ENSRNOP00000087612
1 to 30 of 32 rows
1 to 5 of 29 rows
1 to 5 of 29 rows
Ensembl Acc Id: ENSRNOP00000051120   ⟸   ENSRNOT00000045534
Ensembl Acc Id: ENSRNOP00000070457   ⟸   ENSRNOT00000087977
Ensembl Acc Id: ENSRNOP00000071468   ⟸   ENSRNOT00000078997
RefSeq Acc Id: NP_001099227   ⟸   NM_001105757
- UniProtKB: A0A8I6GFB1 (UniProtKB/TrEMBL),   A0A0G2JXZ3 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_038955386   ⟸   XM_039099458
- Peptide Label: isoform X1
- UniProtKB: A0A0G2JXZ3 (UniProtKB/TrEMBL)
Name Modeler Protein Id AA Range Protein Structure
AF-P70486-F1-model_v2 AlphaFold P70486 1-527 view protein structure


eQTL   View at Phenogen
WGCNA   View at Phenogen
Tissue/Strain Expression   View at Phenogen

RGD ID:13701901
Promoter ID:EPDNEW_R12421
Type:initiation region
Name:Atrx_1
Description:ATRX, chromatin remodeler
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Rat AssemblyChrPosition (strand)Source
Rnor_6.0X76,979,115 - 76,979,175EPDNEW


1 to 19 of 19 rows
Database
Acc Id
Source(s)
BioCyc Gene G2FUF-1932 BioCyc
Ensembl Genes ENSRNOG00000046897 Ensembl
  ENSRNOG00000056703 Ensembl, ENTREZGENE
Ensembl Transcript ENSRNOT00000087977 ENTREZGENE
  ENSRNOT00000091284 ENTREZGENE
  ENSRNOT00000095781 ENTREZGENE
InterPro ATRX_domain-containing UniProtKB/Swiss-Prot
NCBI Gene 246284 ENTREZGENE
PANTHER TRANSCRIPTIONAL REGULATOR ATRX UniProtKB/Swiss-Prot
  TRANSCRIPTIONAL REGULATOR ATRX UniProtKB/Swiss-Prot
PhenoGen Atrx PhenoGen
RatGTEx ENSRNOG00000046897 RatGTEx
  ENSRNOG00000056703 RatGTEx
UniProt A0A0G2JXZ3 ENTREZGENE, UniProtKB/TrEMBL
  A0A0G2K0J1_RAT UniProtKB/TrEMBL
  A0A8I6A4N1 ENTREZGENE, UniProtKB/TrEMBL
  A0A8I6GFB1 ENTREZGENE, UniProtKB/TrEMBL
  A6IV35_RAT UniProtKB/TrEMBL
  ATRX_RAT UniProtKB/Swiss-Prot, ENTREZGENE
1 to 19 of 19 rows


Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2021-03-09 Atrx  ATRX, chromatin remodeler  LOC103690008  transcriptional regulator ATRX-like  Data merged from RGD:9140280 737654 PROVISIONAL
2016-06-01 Atrx  ATRX, chromatin remodeler  Atrx  alpha thalassemia/mental retardation syndrome X-linked  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2014-08-25 LOC103690008  transcriptional regulator ATRX-like      Symbol and Name status set to provisional 70820 PROVISIONAL
2011-07-28 Atrx  alpha thalassemia/mental retardation syndrome X-linked  Atrx  alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2008-09-25 Atrx  alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S. cerevisiae)  Atrx  alpha thalassemia/mental retardation syndrome X-linked homolog (human)  Nomenclature updated to reflect human and mouse nomenclature 1299863 APPROVED
2005-01-20 Atrx  alpha thalassemia/mental retardation syndrome X-linked homolog (human)    alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S.cerevisiae)  Name updated 1299863 APPROVED
2002-08-07 Atrx  alpha thalassemia/mental retardation syndrome X-linked (RAD54 homolog, S.cerevisiae)      Symbol and Name status set to provisional 70820 PROVISIONAL

Note Type Note Reference
gene_homology high homology with human X-linked Helicase2 (XH2) 631943