Details for: NHS

Gene ID: 4810

Symbol: NHS

Ensembl ID: ENSG00000188158

Description: NHS actin remodeling regulator

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: stromal cell of bone marrow (CL0010001)
    Fold Change: 9.5108
    Cell Significance Index: -37.5300
  • Cell Name: epidermal Langerhans cell (CL0002457)
    Fold Change: 8.8185
    Cell Significance Index: -19.3000
  • Cell Name: epithelial cell of prostate (CL0002231)
    Fold Change: 4.4962
    Cell Significance Index: 27.7400
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: 3.7374
    Cell Significance Index: 100.1500
  • Cell Name: basal epithelial cell of prostatic duct (CL0002236)
    Fold Change: 3.4303
    Cell Significance Index: 30.4500
  • Cell Name: leptomeningeal cell (CL0000708)
    Fold Change: 3.1518
    Cell Significance Index: 67.3700
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: 3.0833
    Cell Significance Index: 173.0200
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: 2.9853
    Cell Significance Index: 40.7300
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 2.7493
    Cell Significance Index: 986.1200
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: 2.2124
    Cell Significance Index: 61.8300
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: 2.0818
    Cell Significance Index: 127.9600
  • Cell Name: hippocampal interneuron (CL1001569)
    Fold Change: 1.9254
    Cell Significance Index: 24.9700
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: 1.7834
    Cell Significance Index: 42.7700
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 1.5911
    Cell Significance Index: 1100.4800
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 1.4893
    Cell Significance Index: 2025.0300
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: 1.4034
    Cell Significance Index: 72.9100
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 1.0712
    Cell Significance Index: 105.9700
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 1.0500
    Cell Significance Index: 666.8500
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: 0.8562
    Cell Significance Index: 16.7100
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: 0.8470
    Cell Significance Index: 53.3900
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: 0.7533
    Cell Significance Index: 26.4700
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.7369
    Cell Significance Index: 665.3600
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.7352
    Cell Significance Index: 1131.7700
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.6751
    Cell Significance Index: 135.4300
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.6430
    Cell Significance Index: 1210.6100
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.5586
    Cell Significance Index: 90.8500
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.4753
    Cell Significance Index: 876.6300
  • Cell Name: subcutaneous adipocyte (CL0002521)
    Fold Change: 0.4388
    Cell Significance Index: 1.9100
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.4284
    Cell Significance Index: 85.0100
  • Cell Name: midget ganglion cell of retina (CL4023188)
    Fold Change: 0.4070
    Cell Significance Index: 4.2400
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.3840
    Cell Significance Index: 41.7700
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 0.3512
    Cell Significance Index: 8.7800
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.2594
    Cell Significance Index: 46.7700
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.2125
    Cell Significance Index: 26.1300
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 0.1934
    Cell Significance Index: 14.8400
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: 0.1779
    Cell Significance Index: 80.7600
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.1339
    Cell Significance Index: 73.1100
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.1264
    Cell Significance Index: 24.0600
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: 0.1228
    Cell Significance Index: 2.6600
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.0944
    Cell Significance Index: 2.7200
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.0894
    Cell Significance Index: 5.3700
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.0760
    Cell Significance Index: 3.4500
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.0606
    Cell Significance Index: 8.3200
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 0.0598
    Cell Significance Index: 7.6700
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: 0.0557
    Cell Significance Index: 34.7700
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.0429
    Cell Significance Index: 2.9700
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 0.0382
    Cell Significance Index: 2.5700
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.0316
    Cell Significance Index: 13.9900
  • Cell Name: OFF midget ganglion cell (CL4033047)
    Fold Change: 0.0144
    Cell Significance Index: 0.1800
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: -0.0037
    Cell Significance Index: -0.1000
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.0158
    Cell Significance Index: -2.2900
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0176
    Cell Significance Index: -12.9000
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0254
    Cell Significance Index: -18.8200
  • Cell Name: adipocyte of breast (CL0002617)
    Fold Change: -0.0270
    Cell Significance Index: -0.3400
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0329
    Cell Significance Index: -18.5800
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -0.0458
    Cell Significance Index: -0.9200
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0510
    Cell Significance Index: -38.6200
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.1034
    Cell Significance Index: -21.7700
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.1086
    Cell Significance Index: -31.2500
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.1110
    Cell Significance Index: -12.9300
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.1168
    Cell Significance Index: -19.9400
  • Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
    Fold Change: -0.1665
    Cell Significance Index: -2.3900
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.1769
    Cell Significance Index: -18.4200
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.2389
    Cell Significance Index: -5.0700
  • Cell Name: ON midget ganglion cell (CL4033046)
    Fold Change: -0.2504
    Cell Significance Index: -3.1600
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.2678
    Cell Significance Index: -16.4200
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.2793
    Cell Significance Index: -36.0800
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.2822
    Cell Significance Index: -28.8300
  • Cell Name: pancreatic endocrine cell (CL0008024)
    Fold Change: -0.3137
    Cell Significance Index: -35.8100
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.3154
    Cell Significance Index: -36.1400
  • Cell Name: chandelier cell (CL4023083)
    Fold Change: -0.3171
    Cell Significance Index: -2.5600
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.3243
    Cell Significance Index: -15.2400
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.3548
    Cell Significance Index: -18.6300
  • Cell Name: sst GABAergic cortical interneuron (CL4023017)
    Fold Change: -0.3560
    Cell Significance Index: -7.0400
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: -0.3573
    Cell Significance Index: -25.2700
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.3611
    Cell Significance Index: -7.6900
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.3973
    Cell Significance Index: -12.7300
  • Cell Name: retinal rod cell (CL0000604)
    Fold Change: -0.4136
    Cell Significance Index: -4.9300
  • Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
    Fold Change: -0.4161
    Cell Significance Index: -8.9900
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: -0.4499
    Cell Significance Index: -5.5800
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.4573
    Cell Significance Index: -36.2200
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.4876
    Cell Significance Index: -36.3400
  • Cell Name: lens fiber cell (CL0011004)
    Fold Change: -0.5103
    Cell Significance Index: -16.1400
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: -0.5883
    Cell Significance Index: -26.0200
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.5967
    Cell Significance Index: -27.8200
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.6070
    Cell Significance Index: -39.1600
  • Cell Name: chandelier pvalb GABAergic cortical interneuron (CL4023036)
    Fold Change: -0.6138
    Cell Significance Index: -12.8100
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: -0.6197
    Cell Significance Index: -10.6200
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.6203
    Cell Significance Index: -32.3100
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.6213
    Cell Significance Index: -20.3400
  • Cell Name: fibroblast of cardiac tissue (CL0002548)
    Fold Change: -0.6316
    Cell Significance Index: -9.0700
  • Cell Name: epithelial cell of proximal tubule (CL0002306)
    Fold Change: -0.6423
    Cell Significance Index: -4.9100
  • Cell Name: inhibitory interneuron (CL0000498)
    Fold Change: -0.6485
    Cell Significance Index: -7.7600
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.7119
    Cell Significance Index: -24.9400
  • Cell Name: umbrella cell of urothelium (CL4030056)
    Fold Change: -0.7276
    Cell Significance Index: -6.7000
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.7636
    Cell Significance Index: -21.7900
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.7883
    Cell Significance Index: -25.1100
  • Cell Name: kidney loop of Henle thick ascending limb epithelial cell (CL1001106)
    Fold Change: -0.8001
    Cell Significance Index: -7.2100
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: -0.8078
    Cell Significance Index: -30.5900
  • Cell Name: skeletal muscle fibroblast (CL0011027)
    Fold Change: -0.8324
    Cell Significance Index: -5.6400

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. **Actin Remodeling Regulator:** The NHS gene is a key regulator of actin remodeling, a critical process involved in cell shape, motility, and signaling. 2. **Significantly Expressed Cells:** The NHS gene is expressed in a wide range of cell types, including lens epithelial cells, anterior lens cells, secondary lens fibers, inhibitory interneurons, and other cell types involved in development and maintenance of tissues. 3. **Pathway Involvement:** The NHS gene is involved in several signaling pathways, including the Rac1, Rac2, Rac3, Rho, and Miro GTPase cycles, highlighting its role in regulating cell signaling and actin remodeling. **Pathways and Functions:** The NHS gene is involved in several signaling pathways, including: 1. **Rac1, Rac2, Rac3, and Rho GTPase Cycles:** These pathways are critical for regulating actin remodeling, cell shape, and cell signaling. 2. **Miro GTPase Cycle:** This pathway is involved in regulating mitochondrial dynamics and actin remodeling. 3. **Signaling by Rho GTPases:** The NHS gene is involved in regulating signaling pathways mediated by Rho GTPases, including the Rho-associated protein kinase (ROCK) pathway. 4. **Apical Plasma Membrane and Bicellular Tight Junctions:** The NHS gene is involved in regulating the structure and function of apical plasma membranes and bicellular tight junctions. **Clinical Significance:** The NHS gene's involvement in congenital cataracts and dental anomalies highlights its importance in maintaining tissue integrity and function. Mutations in the NHS gene have been associated with these conditions, demonstrating the gene's critical role in regulating actin remodeling and cell signaling. 1. **Congenital Cataracts and Dental Anomalies:** The NHS gene's association with these conditions highlights the importance of actin remodeling in maintaining lens and dental tissue integrity. 2. **Adrenal Gland and Kidney Development:** The NHS gene's involvement in the development and maintenance of these tissues highlights its role in regulating cell signaling and actin remodeling. 3. **Implications for Disease Treatment:** Understanding the NHS gene's role in actin remodeling and cell signaling has implications for the development of novel therapeutic strategies for diseases associated with actin remodeling dysregulation. In conclusion, the NHS gene plays a critical role in regulating actin remodeling and cell signaling, with implications for maintaining tissue integrity and function. Further research is necessary to fully understand the mechanisms underlying the NHS gene's function and its clinical significance.

Genular Protein ID: 3251572858

Symbol: NHS_HUMAN

Name: Congenital cataracts and dental anomalies protein

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 14564667

Title: Mutations in a novel gene, NHS, cause the pleiotropic effects of Nance-Horan syndrome, including severe congenital cataract, dental anomalies, and mental retardation.

PubMed ID: 14564667

DOI: 10.1086/379381

PubMed ID: 16675532

Title: Nance-Horan syndrome protein, NHS, associates with epithelial cell junctions.

PubMed ID: 16675532

DOI: 10.1093/hmg/ddl120

PubMed ID: 15772651

Title: The DNA sequence of the human X chromosome.

PubMed ID: 15772651

DOI: 10.1038/nature03440

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: 17974005

Title: The full-ORF clone resource of the German cDNA consortium.

PubMed ID: 17974005

DOI: 10.1186/1471-2164-8-399

PubMed ID: 15466011

Title: Identification of the gene for Nance-Horan syndrome (NHS).

PubMed ID: 15466011

DOI: 10.1136/jmg.2004.022517

PubMed ID: 16964243

Title: A probability-based approach for high-throughput protein phosphorylation analysis and site localization.

PubMed ID: 16964243

DOI: 10.1038/nbt1240

PubMed ID: 18669648

Title: A quantitative atlas of mitotic phosphorylation.

PubMed ID: 18669648

DOI: 10.1073/pnas.0805139105

PubMed ID: 19447104

Title: NHS-A isoform of the NHS gene is a novel interactor of ZO-1.

PubMed ID: 19447104

DOI: 10.1016/j.yexcr.2009.05.008

PubMed ID: 19414485

Title: X-linked cataract and Nance-Horan syndrome are allelic disorders.

PubMed ID: 19414485

DOI: 10.1093/hmg/ddp206

PubMed ID: 20332100

Title: The Nance-Horan syndrome protein encodes a functional WAVE homology domain (WHD) and is important for co-ordinating actin remodelling and maintaining cell morphology.

PubMed ID: 20332100

DOI: 10.1093/hmg/ddq125

PubMed ID: 23186163

Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.

PubMed ID: 23186163

DOI: 10.1021/pr300630k

PubMed ID: 16959974

Title: The consensus coding sequences of human breast and colorectal cancers.

PubMed ID: 16959974

DOI: 10.1126/science.1133427

PubMed ID: 23092983

Title: Analysis of the chromosome X exome in patients with autism spectrum disorders identified novel candidate genes, including TMLHE.

PubMed ID: 23092983

DOI: 10.1038/tp.2012.102

PubMed ID: 26566883

Title: Homozygous missense mutation in the LMAN2L gene segregates with intellectual disability in a large consanguineous Pakistani family.

PubMed ID: 26566883

DOI: 10.1136/jmedgenet-2015-103179

Sequence Information:

  • Length: 1651
  • Mass: 179135
  • Checksum: 9B98C97BA0109F82
  • Sequence:
  • MPFAKRIVEP QWLCRQRRPA PGPAVDASGG SAEPPPPLQP PGRRDLDEVE APGPEEPARA 
    VPAPSGLPPP PPPLPAPADQ TQPPHGEASV AGEESTAGIP EAAPAAGEAS SAAAAAAVLL 
    MLDLCAVSNA ALARVLRQLS DVARHACSLF QELESDIQLT HRRVWALQGK LGGVQRVLST 
    LDPKQEAVPV SNLDIESKLS VYYRAPWHQQ RNIFLPATRP PCVEELHRHA RQSLQALRRE 
    HRSRSDRREQ RAAAPLSIAA PPLPAYPPAH SQRRREFKDR HFLTFNSTRS PSPTECCHMT 
    PWSRKSHPPE DEDTDVMLGQ RPKNPIHNIP STLDKQTNWS KALPLPTPEE KMKQDAQVIS 
    SCIIPINVTG VGFDREASIR CSLVHSQSVL QRRRKLRRRK TISGIPRRVQ QEIDSDESPV 
    ARERNVIVHT NPDPSNTVNR ISGTRDSECQ TEDILIAAPS RRRIRAQRGQ SIAASLSHSA 
    GNISALADKG DTMFTPAVSS RTRSRSLPRE GNRGGDAEPK VGAKPSAYEE GESFVGDHER 
    TPNDFSEAPS SPSAQDHQPT LGLACSQHLH SPQHKLSERG RSRLSRMAAD SGSCDISSNS 
    DTFGSPIHCI STAGVLLSSH MDQKDDHQSS SGNWSGSSST CPSQTSETIP PAASPPLTGS 
    SHCDSELSLN TAPHANEDAS VFVTEQYNDH LDKVRGHRAN SFTSTVADLL DDPNNSNTSD 
    SEWNYLHHHH DASCRQDFSP ERPKADSLGC PSFTSMATYD SFLEKSPSDK ADTSSHFSVD 
    TEGYYTSMHF DCGLKGNKSY VCHYAALGPE NGQGVGASPG LPDCAWQDYL DHKRQGRPSI 
    SFRKPKAKPT PPKRSSSLRK SDGNADISEK KEPKISSGQH LPHSSREMKL PLDFANTPSR 
    MENANLPTKQ EPSWINQSEQ GIKEPQLDAS DIPPFKDEVA ESTHYADLWL LNDLKTNDPY 
    RSLSNSSTAT GTTVIECIKS PESSESQTSQ SESRATTPSL PSVDNEFKLA SPEKLAGLAS 
    PSSGYSSQSE TPTSSFPTAF FSGPLSPGGS KRKPKVPERK SSLQQPSLKD GTISLSKDLE 
    LPIIPPTHLD LSALHNVLNK PFHHRHPLHV FTHNKQNTVG ETLRSNPPPS LAITPTILKS 
    VNLRSINKSE EVKQKEENNT DLPYLEESTL TTAALSPSKI RPHTANKSVS RQYSTEDTIL 
    SFLDSSAVEM GPDKLHLEKN STFDVKNRCD PETITSAGSS LLDSNVTKDQ VRTETEPIPE 
    NTPTKNCAFP TEGFQRVSAA RPNDLDGKII QYGPGPDETL EQVQKAPSAG LEEVAQPESV 
    DVITSQSDSP TRATDVSNQF KHQFVMSRHH DKVPGTISYE SEITSVNSFP EKCSKQENIA 
    SGISAKSASD NSKAEETQGN VDEASLKESS PSDDSIISPL SEDSQAEAEG VFVSPNKPRT 
    TEDLFAVIHR SKRKVLGRKD SGDMSVRSKS RAPLSSSSSS ASSITSPSSN VTTPNSQRSP 
    GLIYRNAKKS NTSNEEFKLL LLKKGSRSDS SYRMSATEIL KSPILPKPPG ELTAESPQST 
    DDAHQGSQGA EALSPLSPCS PRVNAEGFSS KSFATSASAR VGRSRAPPAA SSSRYSVRCR 
    LYNTPMQAIS EGETENSDGS PHDDRSSQSS T

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.