Human Gene CR1 (ENST00000367049.9_8) from GENCODE V47lift37
  Description: complement C3b/C4b receptor 1 (Knops blood group), transcript variant S (from RefSeq NM_000651.6)
Gencode Transcript: ENST00000367049.9_8
Gencode Gene: ENSG00000203710.12_15
Transcript (Including UTRs)
   Position: hg19 chr1:207,669,502-207,815,110 Size: 145,609 Total Exon Count: 47 Strand: +
Coding Region
   Position: hg19 chr1:207,669,613-207,812,754 Size: 143,142 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 (chr1:207,669,502-207,815,110)mRNA (may differ from genome)Protein (2489 aa)
Gene SorterGenome BrowserOther Species FASTAVisiGeneGene interactionsTable Schema
AlphaFoldBioGPSEnsemblEntrez GeneExonPrimerGeneCards
HGNCMalacardsMGIOMIMPubMedUniProtKB
WikipediaBioGrid CRISPR DB

-  Comments and Description Text from UniProtKB
  ID: E9PDY4_HUMAN
DESCRIPTION: SubName: Full=Complement receptor type 1;
CAUTION: The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data.

-  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: CR1
Diseases sorted by gene-association score: malaria* (359), plasmodium falciparum malaria (41), follicular dendritic cell sarcoma (24), glomerulonephritis (13), systemic lupus erythematosus (13), histiocytic and dendritic cell cancer (12), alzheimer disease risk factor (12), complement factor i deficiency (11), parapharyngeal meningioma (11), viral pneumonia (10), dendritic cell tumor (10), arthus reaction (9), thyroid crisis (8), proliferative glomerulonephritis (8), castleman disease (8), interdigitating dendritic cell sarcoma (8), t-cell/histiocyte rich large b cell lymphoma (7), hemoglobinuria (7), variola minor (7), follicular lymphoma (6), inflammatory myofibroblastic tumor (6), reticulum cell sarcoma (6), langerhans cell sarcoma (6), afibrinogenemia, congenital (5), afibrinogenemia (5), lateral medullary syndrome (5), histiocytic sarcoma (5), mycetoma (5), hemophagocytic lymphohistiocytosis (2), leukemia, acute myeloid (1)
* = 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
  Press "+" in the title bar above to open this section.

-  RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
  Highest median expression: 16.50 RPKM in Whole Blood
Total median expression: 47.20 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 -23.40111-0.211 Picture PostScript Text
3' UTR -566.502356-0.240 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
IPR016060 - Complement_control_module
IPR000436 - Sushi_SCR_CCP

Pfam Domains:
PF00084 - Sushi repeat (SCR repeat)

SCOP Domains:
50370 - Ricin B-like lectins
101908 - Putative isomerase YbhE
50978 - WD40 repeat-like
69635 - Type III secretory system chaperone-like
55287 - RPB5-like RNA polymerase subunit
57535 - Complement control module/SCR domain
57196 - EGF/Laminin

ModBase Predicted Comparative 3D Structure on E9PDY4
FrontTopSide
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 orthologNo ortholog
Gene DetailsGene Details    
Gene SorterGene Sorter    
 RGD    
      
      

-  Gene Ontology (GO) Annotations with Structured Vocabulary
  Cellular Component:
GO:0016020 membrane
GO:0016021 integral component of membrane


-  Descriptions from all associated GenBank mRNAs
  LP895160 - Sequence 24 from Patent EP3253886.
LP895735 - Sequence 599 from Patent EP3253886.
Y00816 - Human mRNA for complement receptor type 1 (CR1, C3b/C4b receptor, CD35).
BC032550 - Homo sapiens cDNA clone IMAGE:5554371.
X05309 - Human mRNA for C3b/C4b receptor (CR1) F allotype.
AK309342 - Homo sapiens cDNA, FLJ99383.
JD521180 - Sequence 502204 from Patent EP1572962.
AK298486 - Homo sapiens cDNA FLJ57885 complete cds, highly similar to Complement receptor type 1 precursor.
X14362 - Human CR1 mRNA for C3b/C4b receptor secreted form.
JD127331 - Sequence 108355 from Patent EP1572962.
JD355830 - Sequence 336854 from Patent EP1572962.
JD221215 - Sequence 202239 from Patent EP1572962.
JD127331 - Sequence 108355 from Patent EP1572962.
JD355830 - Sequence 336854 from Patent EP1572962.
JD221215 - Sequence 202239 from Patent EP1572962.
AH002679 - Homo sapiens CR1 receptor (CR1) mRNA, partial cds.
JD127331 - Sequence 108355 from Patent EP1572962.
JD355830 - Sequence 336854 from Patent EP1572962.
JD221215 - Sequence 202239 from Patent EP1572962.
JD528349 - Sequence 509373 from Patent EP1572962.
JD365397 - Sequence 346421 from Patent EP1572962.
JD355830 - Sequence 336854 from Patent EP1572962.
JD221215 - Sequence 202239 from Patent EP1572962.
JD127331 - Sequence 108355 from Patent EP1572962.
JD365397 - Sequence 346421 from Patent EP1572962.
JD355830 - Sequence 336854 from Patent EP1572962.
JD221215 - Sequence 202239 from Patent EP1572962.
JD508090 - Sequence 489114 from Patent EP1572962.
JD068780 - Sequence 49804 from Patent EP1572962.
JD227368 - Sequence 208392 from Patent EP1572962.
JD316887 - Sequence 297911 from Patent EP1572962.
JD310754 - Sequence 291778 from Patent EP1572962.
JD502471 - Sequence 483495 from Patent EP1572962.
JD374987 - Sequence 356011 from Patent EP1572962.
JD284174 - Sequence 265198 from Patent EP1572962.
JD374760 - Sequence 355784 from Patent EP1572962.
JD346302 - Sequence 327326 from Patent EP1572962.
JD226846 - Sequence 207870 from Patent EP1572962.
JD519148 - Sequence 500172 from Patent EP1572962.
JD409349 - Sequence 390373 from Patent EP1572962.
JD545293 - Sequence 526317 from Patent EP1572962.
JD173843 - Sequence 154867 from Patent EP1572962.
JD333135 - Sequence 314159 from Patent EP1572962.
JD058781 - Sequence 39805 from Patent EP1572962.
JD318052 - Sequence 299076 from Patent EP1572962.
JD256537 - Sequence 237561 from Patent EP1572962.
JD560687 - Sequence 541711 from Patent EP1572962.
JD476721 - Sequence 457745 from Patent EP1572962.
JD397043 - Sequence 378067 from Patent EP1572962.
JD414790 - Sequence 395814 from Patent EP1572962.
JD414791 - Sequence 395815 from Patent EP1572962.
JD414792 - Sequence 395816 from Patent EP1572962.
JD120549 - Sequence 101573 from Patent EP1572962.
JD120550 - Sequence 101574 from Patent EP1572962.
JD379644 - Sequence 360668 from Patent EP1572962.
JD379645 - Sequence 360669 from Patent EP1572962.
JD379646 - Sequence 360670 from Patent EP1572962.
JD094107 - Sequence 75131 from Patent EP1572962.
JD106881 - Sequence 87905 from Patent EP1572962.
JD553879 - Sequence 534903 from Patent EP1572962.

-  Biochemical and Signaling Pathways
  BioCarta from NCI Cancer Genome Anatomy Project
h_blymphocytePathway - B Lymphocyte Cell Surface Molecules

-  Other Names for This Gene
  Alternate Gene Symbols: CR1 , E9PDY4, E9PDY4_HUMAN, ENST00000367049.1, ENST00000367049.2, ENST00000367049.3, ENST00000367049.4, ENST00000367049.5, ENST00000367049.6, ENST00000367049.7, ENST00000367049.8, NM_000651, uc318fox.1, uc318fox.2
UCSC ID: ENST00000367049.9_8
RefSeq Accession: NM_000651.6
Protein: E9PDY4

-  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.