Human Gene GAR1 (ENST00000226796.7_4) from GENCODE V47lift37
  Description: GAR1 ribonucleoprotein, transcript variant 1 (from RefSeq NM_018983.4)
Gencode Transcript: ENST00000226796.7_4
Gencode Gene: ENSG00000109534.17_7
Transcript (Including UTRs)
   Position: hg19 chr4:110,736,918-110,745,893 Size: 8,976 Total Exon Count: 7 Strand: +
Coding Region
   Position: hg19 chr4:110,737,321-110,745,587 Size: 8,267 Coding Exon Count: 6 

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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 (chr4:110,736,918-110,745,893)mRNA (may differ from genome)Protein (217 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
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UniProtKBWikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: GAR1_HUMAN
DESCRIPTION: RecName: Full=H/ACA ribonucleoprotein complex subunit 1; AltName: Full=Nucleolar protein family A member 1; AltName: Full=snoRNP protein GAR1;
FUNCTION: Required for ribosome biogenesis and telomere maintenance. Part of the H/ACA small nucleolar ribonucleoprotein (H/ACA snoRNP) complex, which catalyzes pseudouridylation of rRNA. This involves the isomerization of uridine such that the ribose is subsequently attached to C5, instead of the normal N1. Each rRNA can contain up to 100 pseudouridine ("psi") residues, which may serve to stabilize the conformation of rRNAs. May also be required for correct processing or intranuclear trafficking of TERC, the RNA component of the telomerase reverse transcriptase (TERT) holoenzyme.
SUBUNIT: Part of the H/ACA small nucleolar ribonucleoprotein (H/ACA snoRNP) complex, which contains NHP2/NOLA2, GAR1/NOLA1, NOP10/NOLA3, and DKC1/NOLA4, which is presumed to be the catalytic subunit. The complex contains a stable core formed by binding of one or two NOP10-DKC1 heterodimers to NHP2; GAR1 subsequently binds to this core via DKC1. The complex binds a box H/ACA small nucleolar RNA (snoRNA), which may target the specific site of modification within the RNA substrate. The complex also interacts with TERC, which contains a 3'-terminal domain related to the box H/ACA snoRNAs. Specific interactions with snoRNAs or TERC are mediated by GAR1 and NHP2. Associates with NOLC1/NOPP140. H/ACA snoRNPs interact with the SMN complex, consisting of SMN1 or SMN2, GEMIN2/SIP1, DDX20/GEMIN3, and GEMIN4. This is mediated by interaction between GAR1 and SMN1 or SMN2. The SMN complex may be required for correct assembly of the H/ACA snoRNP complex. Component of the telomerase holoenzyme complex at least composed of TERT, DKC1, WRAP53/TCAB1, NOP10, NHP2, GAR1, TEP1, EST1A, POT1 and a telomerase RNA template component (TERC).
SUBCELLULAR LOCATION: Nucleus, nucleolus. Nucleus, Cajal body. Note=Also localized to Cajal bodies (coiled bodies).
DOMAIN: Interaction with SMN1 requires at least one of the RGG-box regions.
SIMILARITY: Belongs to the GAR1 family.

-  Primer design for this transcript
 

Primer3Plus can design qPCR Primers that straddle exon-exon-junctions, which amplify only cDNA, not genomic DNA.
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.
Click here to open Exonprimer with this transcript

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: GAR1
Diseases sorted by gene-association score: dyskeratosis congenita (4), spinal muscular atrophy (3), aplastic anemia (2)

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

+  Common Gene Haplotype Alleles
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 17.69 RPKM in Cells - EBV-transformed lymphocytes
Total median expression: 400.25 RPKM



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

+  Microarray Expression Data
  Press "+" in the title bar above to open this section.

-  mRNA Secondary Structure of 3' and 5' UTRs
 
RegionFold EnergyBasesEnergy/Base
Display As
5' UTR -17.2055-0.313 Picture PostScript Text
3' UTR -71.10306-0.232 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
IPR007504 - H/ACA_rnp_Gar1/Naf1
IPR021154 - H/ACA_rnp_Gar1_euk
IPR009000 - Transl_elong_init/rib_B-barrel

Pfam Domains:
PF04410 - Gar1/Naf1 RNA binding region

SCOP Domains:
50447 - Translation proteins

ModBase Predicted Comparative 3D Structure on Q9NY12
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The pictures above may be empty if there is no ModBase structure for the protein. The ModBase structure frequently covers just a fragment of the protein. You may be asked to log onto ModBase the first time you click on the pictures. It is simplest after logging in to just click on the picture again to get to the specific info on that model.

-  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 orthologNo orthologGenome Browser
Gene DetailsGene Details Gene Details Gene Details
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 RGDEnsembl  SGD
     Protein Sequence
     Alignment

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Molecular Function:
GO:0003723 RNA binding
GO:0005515 protein binding
GO:0034513 box H/ACA snoRNA binding
GO:0070034 telomerase RNA binding

Biological Process:
GO:0000454 snoRNA guided rRNA pseudouridine synthesis
GO:0001522 pseudouridine synthesis
GO:0006364 rRNA processing
GO:0007004 telomere maintenance via telomerase
GO:0042254 ribosome biogenesis

Cellular Component:
GO:0000784 nuclear chromosome, telomeric region
GO:0001650 fibrillar center
GO:0005634 nucleus
GO:0005654 nucleoplasm
GO:0005697 telomerase holoenzyme complex
GO:0005730 nucleolus
GO:0015030 Cajal body
GO:0031429 box H/ACA snoRNP complex
GO:0072589 box H/ACA scaRNP complex
GO:0090661 box H/ACA telomerase RNP complex


-  Descriptions from all associated GenBank mRNAs
  BC003413 - Homo sapiens GAR1 ribonucleoprotein homolog (yeast), mRNA (cDNA clone MGC:4917 IMAGE:3451136), complete cds.
AJ276003 - Homo sapiens mRNA for GAR1 protein (GAR1 gene).
AK310489 - Homo sapiens cDNA, FLJ17531.
JD178031 - Sequence 159055 from Patent EP1572962.
JD440117 - Sequence 421141 from Patent EP1572962.
JD442120 - Sequence 423144 from Patent EP1572962.
KJ898980 - Synthetic construct Homo sapiens clone ccsbBroadEn_08374 GAR1 gene, encodes complete protein.
AY780787 - Homo sapiens chromosome 4 nucleolar protein family A member 1 (NOLA1) mRNA, complete cds, alternatively spliced.
DQ894157 - Synthetic construct Homo sapiens clone IMAGE:100008617; FLH168229.01L; RZPDo839D1091D nucleolar protein family A, member 1 (H/ACA small nucleolar RNPs) (NOLA1) gene, encodes complete protein.
EU176271 - Synthetic construct Homo sapiens clone IMAGE:100006560; FLH263554.01X; RZPDo839A11250D nucleolar protein family A, member 1 (H/ACA small nucleolar RNPs) (NOLA1) gene, encodes complete protein.
JD306942 - Sequence 287966 from Patent EP1572962.
JD257935 - Sequence 238959 from Patent EP1572962.
JD551336 - Sequence 532360 from Patent EP1572962.
JD295317 - Sequence 276341 from Patent EP1572962.
JD280270 - Sequence 261294 from Patent EP1572962.
JD081386 - Sequence 62410 from Patent EP1572962.

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

Protein Q9NY12 (Reactome details) participates in the following event(s):

R-HSA-6790905 Box H/ACA snoRNP transforms uridine to pseudouridine in pre-rRNA
R-HSA-6790901 rRNA modification in the nucleus and cytosol
R-HSA-8868773 rRNA processing in the nucleus and cytosol
R-HSA-72312 rRNA processing
R-HSA-8953854 Metabolism of RNA

-  Other Names for This Gene
  Alternate Gene Symbols: ENST00000226796.1, ENST00000226796.2, ENST00000226796.3, ENST00000226796.4, ENST00000226796.5, ENST00000226796.6, GAR1_HUMAN, NM_018983, NOLA1, Q5MJQ2, Q9NY12, uc317dmb.1, uc317dmb.2
UCSC ID: ENST00000226796.7_4
RefSeq Accession: NM_018983.4
Protein: Q9NY12 (aka GAR1_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.