Human Gene ATR (ENST00000350721.9_13) from GENCODE V47lift37
  Description: ATR serine/threonine kinase, transcript variant 1 (from RefSeq NM_001184.4)
Gencode Transcript: ENST00000350721.9_13
Gencode Gene: ENSG00000175054.16_18
Transcript (Including UTRs)
   Position: hg19 chr3:142,168,077-142,297,575 Size: 129,499 Total Exon Count: 47 Strand: -
Coding Region
   Position: hg19 chr3:142,168,271-142,297,546 Size: 129,276 Coding Exon Count: 47 

Page IndexSequence and LinksUniProtKB CommentsPrimersMalaCardsCTD
Gene AllelesRNA-Seq ExpressionMicroarray ExpressionRNA StructureProtein StructureOther Species
GO AnnotationsmRNA DescriptionsPathwaysOther NamesModel InformationMethods
Data last updated at UCSC: 2024-08-22 23:36:26

-  Sequence and Links to Tools and Databases
 
Genomic Sequence (chr3:142,168,077-142,297,575)mRNA (may differ from genome)Protein (2644 aa)
Gene SorterGenome BrowserOther Species FASTAGene interactionsTable SchemaAlphaFold
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-  Comments and Description Text from UniProtKB
  ID: ATR_HUMAN
DESCRIPTION: RecName: Full=Serine/threonine-protein kinase ATR; EC=2.7.11.1; AltName: Full=Ataxia telangiectasia and Rad3-related protein; AltName: Full=FRAP-related protein 1;
FUNCTION: Serine/threonine protein kinase which activates checkpoint signaling upon genotoxic stresses such as ionizing radiation (IR), ultraviolet light (UV), or DNA replication stalling, thereby acting as a DNA damage sensor. Recognizes the substrate consensus sequence [ST]-Q. Phosphorylates BRCA1, CHEK1, MCM2, RAD17, RPA2, SMC1 and p53/TP53, which collectively inhibit DNA replication and mitosis and promote DNA repair, recombination and apoptosis. Phosphorylates 'Ser-139' of histone variant H2AX/H2AFX at sites of DNA damage, thereby regulating DNA damage response mechanism. Required for FANCD2 ubiquitination. Critical for maintenance of fragile site stability and efficient regulation of centrosome duplication.
CATALYTIC ACTIVITY: ATP + a protein = ADP + a phosphoprotein.
COFACTOR: Manganese.
ENZYME REGULATION: Activated by DNA and inhibited by BCR-ABL oncogene. Slightly activated by ATRIP. Inhibited by caffeine, wortmannin and LY294002.
SUBUNIT: Interacts with ATRIP (By similarity). Forms an heterodimer with ATRIP. Binds to DNA, and to UV-damaged DNA with higher affinity. Interacts with RAD17, MSH2 and HDAC2. Present in a complex containing ATRIP and RPA-coated single-stranded DNA. Present in a complex containing CHD4 and HDAC2. Interacts with BCR-ABL after genotoxic stress. Interacts with EEF1E1. This interaction is enhanced by UV irradiation. Interacts with CLSPN and CEP164. Interacts with TELO2 and TTI1.
INTERACTION: O43156:TTI1; NbExp=2; IntAct=EBI-968983, EBI-1055680;
SUBCELLULAR LOCATION: Nucleus. Nucleus, PML body (By similarity). Note=Depending on the cell type, it can also be found in PML nuclear bodies. Recruited to chromatin during S-phase. Redistributes to discrete nuclear foci upon DNA damage, hypoxia or replication fork stalling.
TISSUE SPECIFICITY: Ubiquitous, with highest expression in testis. Isoform 2 is found in pancreas, placenta and liver but not in heart, testis and ovary.
PTM: Phosphorylated; autophosphorylates in vitro.
DISEASE: Defects in ATR are a cause of Seckel syndrome type 1 (SCKL1) [MIM:210600]. SCKL1 is a rare autosomal recessive disorder characterized by growth retardation, microcephaly with mental retardation, and a characteristic 'bird-headed' facial appearance.
DISEASE: Defects in ATR are the cause of cutaneous telangiectasia and cancer syndrome, familial (FCTCS) [MIM:614564]. A disease characterized by cutaneous telangiectases in infancy with patchy alopecia over areas of affected skin, thinning of the lateral eyebrows, and mild dental and nail anomalies. Affected individuals are at increased risk of developing oropharyngeal cancer, and other malignancies have been reported as well.
SIMILARITY: Belongs to the PI3/PI4-kinase family. ATM subfamily.
SIMILARITY: Contains 1 FAT domain.
SIMILARITY: Contains 1 FATC domain.
SIMILARITY: Contains 2 HEAT repeats.
SIMILARITY: Contains 1 PI3K/PI4K domain.
WEB RESOURCE: Name=GeneReviews; URL="http://www.ncbi.nlm.nih.gov/sites/GeneTests/lab/gene/ATR";

-  Primer design for this transcript
 

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Click here to load the transcript sequence and exon structure into Primer3Plus

Exonprimer can design one pair of Sanger sequencing primers around every exon, located in non-genic sequence.
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To design primers for a non-coding sequence, zoom to a region of interest and select from the drop-down menu: View > In External Tools > Primer3


-  MalaCards Disease Associations
  MalaCards Gene Search: ATR
Diseases sorted by gene-association score: cutaneous telangiectasia and cancer syndrome, familial* (1729), seckel syndrome 1* (1029), seckel syndrome* (288), ataxia-telangiectasia (64), ataxia (26), bacillary angiomatosis (15), chronic active epstein-barr virus infection (10), israeli tick typhus (9), xeroderma pigmentosum, group a (9), bartonellosis (7), lig4 syndrome (6), lung large cell carcinoma (5), human granulocytic anaplasmosis (4), meier-gorlin syndrome 1 (4), microcephaly (4), breast cancer (2)
* = Manually curated disease association

-  Comparative Toxicogenomics Database (CTD)
  The following chemicals interact with this gene           more ... click here to view the complete list

+  Common Gene Haplotype Alleles
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-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 7.71 RPKM in Adrenal Gland
Total median expression: 150.72 RPKM



View in GTEx track of Genome Browser    View at GTEx portal     View GTEx Body Map

+  Microarray Expression Data
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-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -5.4029-0.186 Picture PostScript Text
3' UTR -25.20194-0.130 Picture PostScript Text

The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.

-  Protein Domain and Structure Information
  InterPro Domains: Graphical view of domain structure
IPR011989 - ARM-like
IPR016024 - ARM-type_fold
IPR003152 - FATC
IPR021133 - HEAT_type_2
IPR011009 - Kinase-like_dom
IPR000403 - PI3/4_kinase_cat_dom
IPR018936 - PI3/4_kinase_CS
IPR003151 - PIK-rel_kinase_FAT
IPR014009 - PIK_FAT
IPR011990 - TPR-like_helical
IPR012993 - UME

Pfam Domains:
PF00454 - Phosphatidylinositol 3- and 4-kinase
PF02259 - FAT domain
PF02260 - FATC domain
PF08064 - UME (NUC010) domain

SCOP Domains:
48371 - ARM repeat
81901 - HCP-like
48431 - Lipovitellin-phosvitin complex, superhelical domain
48452 - TPR-like
56112 - Protein kinase-like (PK-like)

ModBase Predicted Comparative 3D Structure on Q13535
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-  Orthologous Genes in Other Species
  Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
MouseRatZebrafishD. melanogasterC. elegansS. cerevisiae
No orthologNo orthologNo orthologNo orthologGenome BrowserNo ortholog
Gene DetailsGene Details Gene DetailsGene Details 
Gene SorterGene Sorter Gene SorterGene Sorter 
 RGDEnsembl WormBase 
    Protein Sequence 
    Alignment 

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0000166 nucleotide binding
GO:0003677 DNA binding
GO:0004672 protein kinase activity
GO:0004674 protein serine/threonine kinase activity
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0016301 kinase activity
GO:0016740 transferase activity
GO:0032405 MutLalpha complex binding
GO:0032407 MutSalpha complex binding

Biological Process:
GO:0000077 DNA damage checkpoint
GO:0006260 DNA replication
GO:0006281 DNA repair
GO:0006974 cellular response to DNA damage stimulus
GO:0007275 multicellular organism development
GO:0008156 negative regulation of DNA replication
GO:0016310 phosphorylation
GO:0018105 peptidyl-serine phosphorylation
GO:0032212 positive regulation of telomere maintenance via telomerase
GO:0034644 cellular response to UV
GO:0036297 interstrand cross-link repair
GO:0042493 response to drug
GO:0043517 positive regulation of DNA damage response, signal transduction by p53 class mediator
GO:0046777 protein autophosphorylation
GO:0070198 protein localization to chromosome, telomeric region
GO:0071480 cellular response to gamma radiation
GO:0090399 replicative senescence
GO:0097694 establishment of RNA localization to telomere
GO:0097695 establishment of macromolecular complex localization to telomere
GO:1900034 regulation of cellular response to heat
GO:1904884 positive regulation of telomerase catalytic core complex assembly

Cellular Component:
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005694 chromosome
GO:0005794 Golgi apparatus
GO:0016605 PML body
GO:0000784 nuclear chromosome, telomeric region


-  Descriptions from all associated GenBank mRNAs
  LF385524 - JP 2014500723-A/193027: Polycomb-Associated Non-Coding RNAs.
U76308 - Human protein kinase ATR mRNA, complete cds.
Y09077 - H.sapiens mRNA for atr gene.
U49844 - Human FRAP-related protein (FRP1) mRNA, complete cds.
BC172404 - Synthetic construct Homo sapiens clone IMAGE:100069098, MGC:199109 ataxia telangiectasia and Rad3 related (ATR) mRNA, encodes complete protein.
MA621101 - JP 2018138019-A/193027: Polycomb-Associated Non-Coding RNAs.
LF208585 - JP 2014500723-A/16088: Polycomb-Associated Non-Coding RNAs.
AB208847 - Homo sapiens mRNA for ataxia telangiectasia and Rad3 related protein variant protein.
JD109963 - Sequence 90987 from Patent EP1572962.
AK131535 - Homo sapiens cDNA FLJ16765 fis, clone BRAWH3011637.
MA444162 - JP 2018138019-A/16088: Polycomb-Associated Non-Coding RNAs.
JD026114 - Sequence 7138 from Patent EP1572962.
JD033999 - Sequence 15023 from Patent EP1572962.
AK307402 - Homo sapiens cDNA, FLJ97350.

-  Biochemical and Signaling Pathways
  Reactome (by CSHL, EBI, and GO)

Protein Q13535 (Reactome details) participates in the following event(s):

R-HSA-912450 ATR Kinase is recruited to unsynapsed regions
R-HSA-176250 Binding of ATR-ATRIP to the RPA-ssDNA complex
R-HSA-5684875 Binding of ATR:ATRIP to RPA at resected DNA DSBs
R-HSA-6788385 The complex of ATR and ATRIP is recruited to ICL-DNA
R-HSA-5686657 ERCC1:XPF cleaves flaps generated by SSA
R-HSA-5693561 RAD51 binds BRCA2 at resected DNA DSBs
R-HSA-6788392 ATR phosphorylates RPA2, FANCI, FANCD2 and FANCM at ICL-DNA
R-HSA-5685011 ATR activation at DNA DSBs
R-HSA-176116 Recruitment and activation of Chk1
R-HSA-176298 Activation of claspin
R-HSA-912470 ATR phosphorylates Histone H2A.X at unsynapsed regions
R-HSA-3371567 DBC1 is phosphorylated by ATM/ART
R-HSA-5685156 ATR phosphorylates RPA2
R-HSA-5684887 Activation of CHEK1 at resected DNA DSBs
R-HSA-5684882 CHEK1 is recruited to resected DNA DSBs
R-HSA-5693580 Association of RAD52 with the RPA complex at resected DNA DSBs
R-HSA-6799332 ATR phosphorylates TP53
R-HSA-5693564 Association of RAD51 with RAD52:DNA double-strand break ends
R-HSA-5686642 RAD52 promotes single strand annealing at resected DNA DSBs
R-HSA-1221632 Meiotic synapsis
R-HSA-176187 Activation of ATR in response to replication stress
R-HSA-5693607 Processing of DNA double-strand break ends
R-HSA-6783310 Fanconi Anemia Pathway
R-HSA-5685938 HDR through Single Strand Annealing (SSA)
R-HSA-5693616 Presynaptic phase of homologous DNA pairing and strand exchange
R-HSA-6796648 TP53 Regulates Transcription of DNA Repair Genes
R-HSA-1500620 Meiosis
R-HSA-69481 G2/M Checkpoints
R-HSA-5693567 HDR through Homologous Recombination (HR) or Single Strand Annealing (SSA)
R-HSA-73894 DNA Repair
R-HSA-5693579 Homologous DNA Pairing and Strand Exchange
R-HSA-69473 G2/M DNA damage checkpoint
R-HSA-3371453 Regulation of HSF1-mediated heat shock response
R-HSA-3700989 Transcriptional Regulation by TP53
R-HSA-1474165 Reproduction
R-HSA-1640170 Cell Cycle
R-HSA-69620 Cell Cycle Checkpoints
R-HSA-5693538 Homology Directed Repair
R-HSA-5685942 HDR through Homologous Recombination (HRR)
R-HSA-3371556 Cellular response to heat stress
R-HSA-212436 Generic Transcription Pathway
R-HSA-6804756 Regulation of TP53 Activity through Phosphorylation
R-HSA-5693532 DNA Double-Strand Break Repair
R-HSA-2262752 Cellular responses to stress
R-HSA-73857 RNA Polymerase II Transcription
R-HSA-5633007 Regulation of TP53 Activity
R-HSA-8953897 Cellular responses to external stimuli
R-HSA-74160 Gene expression (Transcription)

-  Other Names for This Gene
  Alternate Gene Symbols: ATR , ATR_HUMAN, ENST00000350721.1, ENST00000350721.2, ENST00000350721.3, ENST00000350721.4, ENST00000350721.5, ENST00000350721.6, ENST00000350721.7, ENST00000350721.8, FRP1, NM_001184, Q13535, Q59HB2, Q7KYL3, Q93051, Q9BXK4, uc317yac.1, uc317yac.2
UCSC ID: ENST00000350721.9_13
RefSeq Accession: NM_001184.4
Protein: Q13535 (aka ATR_HUMAN)

-  Gene Model Information
  Click here for a detailed description of the fields of the table above.

-  Methods, Credits, and Use Restrictions
  Click here for details on how this gene model was made and data restrictions if any.