Details for: RHCE

Gene ID: 6006

Symbol: RHCE

Ensembl ID: ENSG00000188672

Description: Rh blood group CcEe antigens

Associated with

Cells (max top 100)

(Cell Significance Index and respective Thresholds are uniquely calculated using our advanced thresholding algorithms to reveal cell-specific gene markers)

  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 18.8848
    Cell Significance Index: -4.7900
  • Cell Name: basophilic erythroblast (CL0000549)
    Fold Change: 8.5199
    Cell Significance Index: 3.8800
  • Cell Name: large intestine goblet cell (CL1000320)
    Fold Change: 0.4780
    Cell Significance Index: 5.1800
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.4311
    Cell Significance Index: 12.4200
  • Cell Name: hepatoblast (CL0005026)
    Fold Change: 0.3255
    Cell Significance Index: 5.4800
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: 0.2705
    Cell Significance Index: 3.6900
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: 0.2398
    Cell Significance Index: 4.1100
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.1874
    Cell Significance Index: 35.6600
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: 0.1712
    Cell Significance Index: 7.9800
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: 0.1508
    Cell Significance Index: 5.7100
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.1494
    Cell Significance Index: 6.6100
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: 0.1370
    Cell Significance Index: 39.4100
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.1324
    Cell Significance Index: 26.5500
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: 0.1269
    Cell Significance Index: 4.4600
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: 0.1126
    Cell Significance Index: 2.4400
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.1036
    Cell Significance Index: 6.2200
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: 0.0673
    Cell Significance Index: 4.2400
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 0.0481
    Cell Significance Index: 3.6900
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.0450
    Cell Significance Index: 4.9000
  • Cell Name: germ cell (CL0000586)
    Fold Change: 0.0417
    Cell Significance Index: 0.3200
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.0356
    Cell Significance Index: 12.7600
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.0333
    Cell Significance Index: 30.0900
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.0299
    Cell Significance Index: 5.9300
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: 0.0255
    Cell Significance Index: 3.7100
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.0092
    Cell Significance Index: 1.6600
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 0.0088
    Cell Significance Index: 0.5900
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.0083
    Cell Significance Index: 0.5800
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: 0.0081
    Cell Significance Index: 0.4200
  • Cell Name: cone retinal bipolar cell (CL0000752)
    Fold Change: 0.0065
    Cell Significance Index: 0.0500
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.0064
    Cell Significance Index: 11.8000
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0063
    Cell Significance Index: 9.7500
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0062
    Cell Significance Index: 11.6400
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0034
    Cell Significance Index: 4.6600
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.0029
    Cell Significance Index: 0.4700
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.0018
    Cell Significance Index: 0.8100
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.0010
    Cell Significance Index: 0.1200
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 0.0005
    Cell Significance Index: 0.3400
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 0.0000
    Cell Significance Index: 0.0000
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: -0.0011
    Cell Significance Index: -0.6200
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0012
    Cell Significance Index: -0.2100
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0023
    Cell Significance Index: -1.0300
  • Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
    Fold Change: -0.0042
    Cell Significance Index: -0.0600
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0045
    Cell Significance Index: -3.3700
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0054
    Cell Significance Index: -3.9600
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0054
    Cell Significance Index: -3.0400
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0059
    Cell Significance Index: -4.4800
  • Cell Name: eukaryotic cell (CL0000255)
    Fold Change: -0.0071
    Cell Significance Index: -0.3100
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0080
    Cell Significance Index: -4.9800
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.0100
    Cell Significance Index: -0.3200
  • Cell Name: lens fiber cell (CL0011004)
    Fold Change: -0.0120
    Cell Significance Index: -0.3800
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: -0.0122
    Cell Significance Index: -1.2000
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.0127
    Cell Significance Index: -0.7800
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: -0.0167
    Cell Significance Index: -2.3000
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.0172
    Cell Significance Index: -0.9100
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: -0.0181
    Cell Significance Index: -0.8200
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.0206
    Cell Significance Index: -1.2600
  • Cell Name: intestinal crypt stem cell of large intestine (CL0009016)
    Fold Change: -0.0217
    Cell Significance Index: -0.1900
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.0217
    Cell Significance Index: -4.5700
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.0246
    Cell Significance Index: -3.1800
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.0251
    Cell Significance Index: -2.9300
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.0252
    Cell Significance Index: -0.7200
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: -0.0265
    Cell Significance Index: -0.7100
  • Cell Name: glutamatergic neuron (CL0000679)
    Fold Change: -0.0275
    Cell Significance Index: -0.3000
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.0305
    Cell Significance Index: -3.4900
  • Cell Name: corneal epithelial cell (CL0000575)
    Fold Change: -0.0316
    Cell Significance Index: -0.4500
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.0329
    Cell Significance Index: -3.3700
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.0389
    Cell Significance Index: -4.5900
  • Cell Name: retinal rod cell (CL0000604)
    Fold Change: -0.0394
    Cell Significance Index: -0.4700
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: -0.0405
    Cell Significance Index: -0.7900
  • Cell Name: primitive red blood cell (CL0002355)
    Fold Change: -0.0415
    Cell Significance Index: -0.4700
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.0427
    Cell Significance Index: -4.4500
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.0470
    Cell Significance Index: -2.6400
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.0484
    Cell Significance Index: -3.6100
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: -0.0501
    Cell Significance Index: -3.5400
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.0546
    Cell Significance Index: -1.7400
  • Cell Name: L6 intratelencephalic projecting glutamatergic neuron of the primary motor cortex (CL4023050)
    Fold Change: -0.0588
    Cell Significance Index: -0.7900
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.0632
    Cell Significance Index: -4.0800
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.0634
    Cell Significance Index: -2.9800
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.0643
    Cell Significance Index: -1.3700
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: -0.0738
    Cell Significance Index: -2.0100
  • Cell Name: type I muscle cell (CL0002211)
    Fold Change: -0.0750
    Cell Significance Index: -1.8300
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: -0.0790
    Cell Significance Index: -0.9800
  • Cell Name: astrocyte of the cerebral cortex (CL0002605)
    Fold Change: -0.0798
    Cell Significance Index: -1.3800
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: -0.0812
    Cell Significance Index: -2.2700
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.0813
    Cell Significance Index: -2.0900
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: -0.0822
    Cell Significance Index: -1.8000
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.0834
    Cell Significance Index: -2.7300
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.0888
    Cell Significance Index: -1.8900
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.0899
    Cell Significance Index: -3.1500
  • Cell Name: OFF midget ganglion cell (CL4033047)
    Fold Change: -0.0986
    Cell Significance Index: -1.2300
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -0.0986
    Cell Significance Index: -3.6200
  • Cell Name: keratocyte (CL0002363)
    Fold Change: -0.0990
    Cell Significance Index: -1.5700
  • Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
    Fold Change: -0.1000
    Cell Significance Index: -2.1600
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: -0.1023
    Cell Significance Index: -1.5100
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: -0.1026
    Cell Significance Index: -2.7400
  • Cell Name: near-projecting glutamatergic cortical neuron (CL4023012)
    Fold Change: -0.1030
    Cell Significance Index: -2.5700
  • Cell Name: epithelial cell of uterus (CL0002149)
    Fold Change: -0.1045
    Cell Significance Index: -1.4500
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: -0.1047
    Cell Significance Index: -2.5100
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -0.1056
    Cell Significance Index: -2.1200
  • Cell Name: CD14-low, CD16-positive monocyte (CL0002396)
    Fold Change: -0.1069
    Cell Significance Index: -2.5900

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this specific cell.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Cell ID: Standard Cell Ontology term used for mapping and comparing cells across experiments. Ensures consistency in analyzing cellular functions across tissues.
Fold Change: Represents the ratio of the current Cell Significance Index to the Cell Significance Index Threshold, indicating how much the gene expression has changed compared to a baseline.
Cell Significance Index: Reflects how strongly a gene is expressed in this cell type. Calculated using techniques like effect size estimation and bootstrapping for reliability.

Other Information

**Key Characteristics:** 1. **RHCE gene encoding**: The RHCE gene encodes for the Rh polypeptide 1, a transmembrane protein that plays a crucial role in the biosynthesis of the Rhesus CcEe antigens. 2. **Rhesus blood group system**: The RHCE gene is a key component of the Rhesus blood group system, which is responsible for the variation in blood type among individuals. 3. **Widespread expression**: The RHCE gene is expressed in various tissues and cell types, including neural progenitor cells, kidney proximal convoluted tubule epithelial cells, and cardiac endothelial cells. 4. **Multiple cellular functions**: The RHCE gene is involved in various cellular processes, including ammonium homeostasis, metabolism, and cell signaling pathways. **Pathways and Functions:** 1. **Ammonium homeostasis**: The RHCE gene is involved in the regulation of ammonium levels in the body, which is essential for maintaining proper acid-base balance and cellular function. 2. **Ankyrin-1 complex**: The RHCE gene interacts with ankyrin-1, a protein that plays a crucial role in maintaining the structure and function of red blood cells. 3. **Blood group systems biosynthesis**: The RHCE gene is involved in the biosynthesis of the Rhesus CcEe antigens, which are responsible for the variation in blood type among individuals. 4. **Metabolism**: The RHCE gene is involved in various metabolic processes, including carbohydrate metabolism and energy production. 5. **Cell signaling pathways**: The RHCE gene interacts with various signaling pathways, including those involved in cell growth, differentiation, and survival. **Clinical Significance:** 1. **Rh incompatibility**: The RHCE gene plays a crucial role in Rh incompatibility, a condition that can lead to hemolytic disease of the newborn (HDN) in Rh-negative mothers carrying Rh-positive fetuses. 2. **Blood transfusion**: The RHCE gene is essential for ensuring safe blood transfusions, as mismatched blood can lead to adverse reactions and complications. 3. **Cancer and immune disorders**: The RHCE gene has been implicated in various cancers and immune disorders, including multiple myeloma and autoimmune diseases. 4. **Neurological disorders**: The RHCE gene has been linked to various neurological disorders, including Alzheimer's disease and Parkinson's disease. In conclusion, the RHCE gene is a critical component of the Rhesus blood group system and plays a pivotal role in various cellular processes. Its clinical significance extends beyond the Rhesus blood group system, with implications for blood transfusion, cancer, immune disorders, and neurological disorders. Further research is needed to fully understand the functions and clinical significance of the RHCE gene.

Genular Protein ID: 1956143753

Symbol: RHCE_HUMAN

Name: Rh polypeptide 1

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 2123099

Title: cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression.

PubMed ID: 2123099

DOI: 10.1042/bj2710821

PubMed ID: 1696722

Title: Molecular cloning and protein structure of a human blood group Rh polypeptide.

PubMed ID: 1696722

DOI: 10.1073/pnas.87.16.6243

PubMed ID: 1379850

Title: Multiple Rh messenger RNA isoforms are produced by alternative splicing.

PubMed ID: 1379850

PubMed ID: 7916743

Title: Isolation of a new cDNA clone encoding an Rh polypeptide associated with the Rh blood group system.

PubMed ID: 7916743

DOI: 10.1007/bf00222717

PubMed ID: 11380456

Title: 16Cys encoded by the RHce gene is associated with altered expression of the e antigen and is frequent in the R0 haplotype.

PubMed ID: 11380456

DOI: 10.1046/j.1365-2141.2001.02803.x

PubMed ID: 11724987

Title: E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop.

PubMed ID: 11724987

DOI: 10.1046/j.1537-2995.2001.41111408.x

PubMed ID: 12393640

Title: Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.

PubMed ID: 12393640

DOI: 10.1182/blood-2002-01-0229

PubMed ID: 16710414

Title: The DNA sequence and biological annotation of human chromosome 1.

PubMed ID: 16710414

DOI: 10.1038/nature04727

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 8188244

Title: Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region.

PubMed ID: 8188244

DOI: 10.1006/geno.1994.1014

PubMed ID: 3146980

Title: Protein-sequence studies on Rh-related polypeptides suggest the presence of at least two groups of proteins which associate in the human red-cell membrane.

PubMed ID: 3146980

DOI: 10.1042/bj2561043

PubMed ID: 3135863

Title: Determination of the N-terminal sequence of human red cell Rh(D) polypeptide and demonstration that the Rh(D), (c), and (E) antigens are carried by distinct polypeptide chains.

PubMed ID: 3135863

PubMed ID: 7789951

Title: Intricate combinatorial patterns of exon splicing generate multiple Rh-related isoforms in human erythroid cells.

PubMed ID: 7789951

DOI: 10.1007/bf00209483

PubMed ID: 8117271

Title: Identification of two Rh mRNA isoforms expressed in immature erythroblasts.

PubMed ID: 8117271

DOI: 10.1006/bbrc.1994.1161

PubMed ID: 1898705

Title: Regarding the size of Rh proteins.

PubMed ID: 1898705

PubMed ID: 9657769

Title: Rhnull disease: the amorph type results from a novel double mutation in RhCe gene on D-negative background.

PubMed ID: 9657769

PubMed ID: 11902138

Title: RHCE represents the ancestral RH position, while RHD is the duplicated gene.

PubMed ID: 11902138

DOI: 10.1182/blood-2001-12-0153

PubMed ID: 25413218

Title: Short duplication within the RHCE gene associated with an in cis deleted RHD causing a Rhnull amorph phenotype in an immunized pregnant woman with anti-Rh29.

PubMed ID: 25413218

DOI: 10.1111/trf.12937

PubMed ID: 35835865

Title: Architecture of the human erythrocyte ankyrin-1 complex.

PubMed ID: 35835865

DOI: 10.1038/s41594-022-00792-w

PubMed ID: 8220426

Title: Molecular genetic basis of the human Rhesus blood group system.

PubMed ID: 8220426

DOI: 10.1038/ng0993-62

Sequence Information:

  • Length: 417
  • Mass: 45451
  • Checksum: 0EEB9D726DB28E6C
  • Sequence:
  • MSSKYPRSVR RCLPLCALTL EAALILLFYF FTHYDASLED QKGLVASYQV GQDLTVMAAL 
    GLGFLTSNFR RHSWSSVAFN LFMLALGVQW AILLDGFLSQ FPPGKVVITL FSIRLATMSA 
    MSVLISAGAV LGKVNLAQLV VMVLVEVTAL GTLRMVISNI FNTDYHMNLR HFYVFAAYFG 
    LTVAWCLPKP LPKGTEDNDQ RATIPSLSAM LGALFLWMFW PSVNSALLRS PIQRKNAMFN 
    TYYALAVSVV TAISGSSLAH PQRKISMTYV HSAVLAGGVA VGTSCHLIPS PWLAMVLGLV 
    AGLISIGGAK CLPVCCNRVL GIHHISVMHS IFSLLGLLGE ITYIVLLVLH TVWNGNGMIG 
    FQVLLSIGEL SLAIVIALTS GLLTGLLLNL KIWKAPHVAK YFDDQVFWKF PHLAVGF

Genular Protein ID: 3460125054

Symbol: A0A220QMN8_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 16181207

Title: Novel weak D types 31 and 32: adsorption-elution-supported D antigen analysis and comparison to prevalent weak D types.

PubMed ID: 16181207

DOI: 10.1111/j.1537-2995.2005.00580.x

PubMed ID: 28671325

Title: Serologic and molecular characterization of weak D type 29.

PubMed ID: 28671325

PubMed ID: 30248182

Title: Two distinct RHCE alleles in cis to weak D type 31 alleles in individuals from different ethnicities.

PubMed ID: 30248182

DOI: 10.1111/trf.14929

Sequence Information:

  • Length: 417
  • Mass: 45534
  • Checksum: C66C8E6D32204964
  • Sequence:
  • MSSKYPRSVR RCLPLWALTL EAALILLFYF FTHYDASLED QKGLVASYQV GQDLTVMAAL 
    GLGFLTSNFR RHSWSSVAFN LFMLALGVQW AILLDGFLSQ FPPGKVVITL FSIRLATMSA 
    MSVLISAGAV LGKVNLAQLV VMVLVEVTAL GTLRMVISNI FNTDYHMNLR HFYVFAAYFG 
    LTVAWCLPKP LPKGTEDNDQ RATIPSLSAM LGALFLWMFW PSVNSALLRS PIQRKNAMFN 
    TYYALAVSVV TAISGSSLAH PQRKISMTYV HSAVLAGGVA VGTSCHLIPS PWLAMVLGLV 
    AGLISIGGAK CLPVCCNRVL GIHHISVMHS IFSLLGLLGE ITYIVLLVLH TVWNGNGMIG 
    FQVLLSIGEL SLAIVIALTS GLLTGLLLNL KIWKAPHVAK YFDDQVFWKF PHLAVGF

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.