Details for: CHRD

Gene ID: 8646

Symbol: CHRD

Ensembl ID: ENSG00000090539

Description: chordin

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: small intestine goblet cell (CL1000495)
    Fold Change: 6.0653
    Cell Significance Index: 213.1300
  • Cell Name: decidual cell (CL2000002)
    Fold Change: 3.8299
    Cell Significance Index: 61.4500
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: 2.8012
    Cell Significance Index: 171.7400
  • Cell Name: microcirculation associated smooth muscle cell (CL0008035)
    Fold Change: 2.6120
    Cell Significance Index: 21.9400
  • Cell Name: hepatoblast (CL0005026)
    Fold Change: 1.5304
    Cell Significance Index: 25.7400
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.8148
    Cell Significance Index: 163.4400
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: 0.7722
    Cell Significance Index: 16.7300
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.7101
    Cell Significance Index: 135.1500
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.5178
    Cell Significance Index: 51.2300
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.4561
    Cell Significance Index: 411.8000
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.4529
    Cell Significance Index: 89.8700
  • Cell Name: keratocyte (CL0002363)
    Fold Change: 0.4274
    Cell Significance Index: 6.7800
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 0.3992
    Cell Significance Index: 26.8500
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.3003
    Cell Significance Index: 41.2400
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.2964
    Cell Significance Index: 106.3100
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: 0.2777
    Cell Significance Index: 7.9600
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: 0.2553
    Cell Significance Index: 5.5900
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.2273
    Cell Significance Index: 36.9700
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: 0.1964
    Cell Significance Index: 5.6100
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 0.1474
    Cell Significance Index: 18.9000
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.1402
    Cell Significance Index: 15.2500
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: 0.1260
    Cell Significance Index: 2.1600
  • Cell Name: fibro/adipogenic progenitor cell (CL0009099)
    Fold Change: 0.1125
    Cell Significance Index: 5.6800
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.0401
    Cell Significance Index: 2.7800
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.0366
    Cell Significance Index: 1.6600
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.0132
    Cell Significance Index: 5.8500
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 0.0003
    Cell Significance Index: 0.1900
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: -0.0035
    Cell Significance Index: -6.6800
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: -0.0097
    Cell Significance Index: -17.8000
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: -0.0113
    Cell Significance Index: -17.3700
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: -0.0118
    Cell Significance Index: -0.3400
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: -0.0120
    Cell Significance Index: -0.3000
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: -0.0131
    Cell Significance Index: -17.8000
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0132
    Cell Significance Index: -2.2500
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: -0.0159
    Cell Significance Index: -8.6800
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0191
    Cell Significance Index: -14.5000
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: -0.0210
    Cell Significance Index: -13.3300
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0211
    Cell Significance Index: -15.6300
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0256
    Cell Significance Index: -14.4400
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0271
    Cell Significance Index: -12.2800
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.0278
    Cell Significance Index: -0.5900
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.0363
    Cell Significance Index: -2.2300
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.0421
    Cell Significance Index: -2.2100
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.0488
    Cell Significance Index: -14.0500
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: -0.0611
    Cell Significance Index: -11.0100
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.0837
    Cell Significance Index: -12.1600
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: -0.0837
    Cell Significance Index: -5.9200
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.0893
    Cell Significance Index: -10.4100
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: -0.1015
    Cell Significance Index: -12.4800
  • Cell Name: periportal region hepatocyte (CL0019026)
    Fold Change: -0.1016
    Cell Significance Index: -1.5000
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.1083
    Cell Significance Index: -13.9900
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: -0.1106
    Cell Significance Index: -6.6400
  • Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
    Fold Change: -0.1115
    Cell Significance Index: -2.4100
  • Cell Name: neuron associated cell (CL0000095)
    Fold Change: -0.1192
    Cell Significance Index: -4.8800
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.1202
    Cell Significance Index: -12.2800
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.1247
    Cell Significance Index: -14.2900
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.1384
    Cell Significance Index: -14.4100
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: -0.1426
    Cell Significance Index: -8.9900
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.1453
    Cell Significance Index: -10.8300
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.1457
    Cell Significance Index: -4.6400
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: -0.1578
    Cell Significance Index: -12.1100
  • Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
    Fold Change: -0.1582
    Cell Significance Index: -2.2700
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.1641
    Cell Significance Index: -7.6500
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.1736
    Cell Significance Index: -5.5600
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.1786
    Cell Significance Index: -14.1500
  • Cell Name: skeletal muscle satellite stem cell (CL0008011)
    Fold Change: -0.1887
    Cell Significance Index: -1.9700
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: -0.1921
    Cell Significance Index: -3.7500
  • Cell Name: centrilobular region hepatocyte (CL0019029)
    Fold Change: -0.2007
    Cell Significance Index: -3.3800
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.2059
    Cell Significance Index: -6.7400
  • Cell Name: sst GABAergic cortical interneuron (CL4023017)
    Fold Change: -0.2094
    Cell Significance Index: -4.1400
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.2204
    Cell Significance Index: -10.3600
  • Cell Name: fibroblast of cardiac tissue (CL0002548)
    Fold Change: -0.2207
    Cell Significance Index: -3.1700
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.2284
    Cell Significance Index: -5.8700
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.2465
    Cell Significance Index: -12.8400
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.2475
    Cell Significance Index: -13.8900
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.2512
    Cell Significance Index: -8.8000
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: -0.2535
    Cell Significance Index: -6.0800
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: -0.2546
    Cell Significance Index: -5.3300
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -0.2645
    Cell Significance Index: -5.3100
  • Cell Name: eukaryotic cell (CL0000255)
    Fold Change: -0.2706
    Cell Significance Index: -11.7700
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -0.2807
    Cell Significance Index: -14.5800
  • Cell Name: transit amplifying cell of small intestine (CL0009012)
    Fold Change: -0.3158
    Cell Significance Index: -6.5500
  • Cell Name: endothelial cell of venule (CL1000414)
    Fold Change: -0.3186
    Cell Significance Index: -3.6200
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.3209
    Cell Significance Index: -6.8400
  • Cell Name: L2/3 intratelencephalic projecting glutamatergic neuron (CL4030059)
    Fold Change: -0.3226
    Cell Significance Index: -4.3000
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: -0.3240
    Cell Significance Index: -14.3300
  • Cell Name: chandelier pvalb GABAergic cortical interneuron (CL4023036)
    Fold Change: -0.3524
    Cell Significance Index: -7.3600
  • Cell Name: cerebral cortex neuron (CL0010012)
    Fold Change: -0.3563
    Cell Significance Index: -3.3900
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: -0.3629
    Cell Significance Index: -13.7400
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -0.3699
    Cell Significance Index: -6.1900
  • Cell Name: helper T cell (CL0000912)
    Fold Change: -0.3744
    Cell Significance Index: -5.3200
  • Cell Name: CD14-low, CD16-positive monocyte (CL0002396)
    Fold Change: -0.3769
    Cell Significance Index: -9.1300
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: -0.3868
    Cell Significance Index: -13.4400
  • Cell Name: BEST4+ enteroycte (CL4030026)
    Fold Change: -0.3962
    Cell Significance Index: -5.9700
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -0.4094
    Cell Significance Index: -15.0300
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: -0.4221
    Cell Significance Index: -11.4900
  • Cell Name: stromal cell of endometrium (CL0002255)
    Fold Change: -0.4415
    Cell Significance Index: -6.2800
  • Cell Name: kidney epithelial cell (CL0002518)
    Fold Change: -0.4485
    Cell Significance Index: -13.2100
  • Cell Name: astrocyte of the cerebral cortex (CL0002605)
    Fold Change: -0.4667
    Cell Significance Index: -8.0700
  • Cell Name: near-projecting glutamatergic cortical neuron (CL4023012)
    Fold Change: -0.4684
    Cell Significance Index: -11.6900

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** The CHRD gene exhibits several key characteristics that highlight its importance in biological processes: 1. **Negative regulation of BMP signaling**: The CHRD protein acts as a negative regulator of the BMP signaling pathway, which is involved in dorsal-ventral patterning, skeletal system development, and floor plate formation. 2. **Widespread expression**: The CHRD gene is expressed in various cell types, including colon goblet cells, mural cells, hepatocytes, granulocyte monocyte progenitor cells, and immature innate lymphoid cells. 3. **Role in cell migration and differentiation**: CHRD has been implicated in the regulation of cell migration and differentiation, particularly in the development of the skeletal system and immune cells. 4. **Potential therapeutic targets**: Abnormal expression or function of the CHRD gene has been linked to several diseases, including cancer, cardiovascular diseases, and neurological disorders, making it a potential therapeutic target for the treatment of these conditions. **Pathways and Functions** The CHRD gene is involved in several key pathways and functions, including: 1. **BMP signaling pathway**: CHRD acts as a negative regulator of the BMP signaling pathway, which is essential for dorsal-ventral patterning, skeletal system development, and floor plate formation. 2. **Cytokine binding**: CHRD has been shown to bind to cytokines, which are signaling molecules that regulate immune responses. 3. **Dorsal/ventral patterning**: CHRD plays a crucial role in the regulation of dorsal-ventral patterning during embryonic development. 4. **Skeletal system development**: CHRD is involved in the regulation of skeletal system development, particularly in the formation of the floor plate and the regulation of osteoblast differentiation. 5. **Cell adhesion and migration**: CHRD has been implicated in the regulation of cell adhesion and migration, particularly in the development of the immune system and the formation of the skeletal system. **Clinical Significance** The CHRD gene has significant clinical implications, including: 1. **Cancer**: Abnormal expression or function of the CHRD gene has been linked to several types of cancer, including osteosarcoma and multiple myeloma. 2. **Cardiovascular diseases**: CHRD has been implicated in the regulation of cardiovascular diseases, including atherosclerosis and cardiac valve disease. 3. **Neurological disorders**: Abnormal expression or function of the CHRD gene has been linked to several neurological disorders, including autism spectrum disorder and schizophrenia. 4. **Immune system dysfunction**: CHRD has been implicated in the regulation of immune system function, particularly in the development of immune cells and the regulation of cytokine signaling. In conclusion, the CHRD gene plays a critical role in regulating various biological processes, including embryonic development, cell migration, and immune function. Abnormal expression or function of the CHRD gene has significant clinical implications, including its link to several diseases, making it a potential therapeutic target for the treatment of these conditions.

Genular Protein ID: 655589212

Symbol: CHRD_HUMAN

Name: Chordin

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11472837

Title: The human chordin gene encodes several differentially expressed spliced variants with distinct BMP opposing activities.

PubMed ID: 11472837

DOI: 10.1016/s0925-4773(01)00423-3

PubMed ID: 12975309

Title: The secreted protein discovery initiative (SPDI), a large-scale effort to identify novel human secreted and transmembrane proteins: a bioinformatics assessment.

PubMed ID: 12975309

DOI: 10.1101/gr.1293003

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: 9782094

Title: Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes.

PubMed ID: 9782094

DOI: 10.1006/geno.1998.5474

PubMed ID: 10648240

Title: BMP-binding modules in chordin: a model for signalling regulation in the extracellular space.

PubMed ID: 10648240

DOI: 10.1242/dev.127.4.821

PubMed ID: 14759258

Title: An unappreciated role for RNA surveillance.

PubMed ID: 14759258

DOI: 10.1186/gb-2004-5-2-r8

Sequence Information:

  • Length: 955
  • Mass: 102032
  • Checksum: 53F9D9F39A517686
  • Sequence:
  • MPSLPAPPAP LLLLGLLLLG SRPARGAGPE PPVLPIRSEK EPLPVRGAAG CTFGGKVYAL 
    DETWHPDLGE PFGVMRCVLC ACEAPQWGRR TRGPGRVSCK NIKPECPTPA CGQPRQLPGH 
    CCQTCPQERS SSERQPSGLS FEYPRDPEHR SYSDRGEPGA EERARGDGHT DFVALLTGPR 
    SQAVARARVS LLRSSLRFSI SYRRLDRPTR IRFSDSNGSV LFEHPAAPTQ DGLVCGVWRA 
    VPRLSLRLLR AEQLHVALVT LTHPSGEVWG PLIRHRALAA ETFSAILTLE GPPQQGVGGI 
    TLLTLSDTED SLHFLLLFRG LLEPRSGGLT QVPLRLQILH QGQLLRELQA NVSAQEPGFA 
    EVLPNLTVQE MDWLVLGELQ MALEWAGRPG LRISGHIAAR KSCDVLQSVL CGADALIPVQ 
    TGAAGSASLT LLGNGSLIYQ VQVVGTSSEV VAMTLETKPQ RRDQRTVLCH MAGLQPGGHT 
    AVGICPGLGA RGAHMLLQNE LFLNVGTKDF PDGELRGHVA ALPYCGHSAR HDTLPVPLAG 
    ALVLPPVKSQ AAGHAWLSLD THCHLHYEVL LAGLGGSEQG TVTAHLLGPP GTPGPRRLLK 
    GFYGSEAQGV VKDLEPELLR HLAKGMASLM ITTKGSPRGE LRGQVHIANQ CEVGGLRLEA 
    AGAEGVRALG APDTASAAPP VVPGLPALAP AKPGGPGRPR DPNTCFFEGQ QRPHGARWAP 
    NYDPLCSLCT CQRRTVICDP VVCPPPSCPH PVQAPDQCCP VCPEKQDVRD LPGLPRSRDP 
    GEGCYFDGDR SWRAAGTRWH PVVPPFGLIK CAVCTCKGGT GEVHCEKVQC PRLACAQPVR 
    VNPTDCCKQC PVGSGAHPQL GDPMQADGPR GCRFAGQWFP ESQSWHPSVP PFGEMSCITC 
    RCGAGVPHCE RDDCSLPLSC GSGKESRCCS RCTAHRRPAP ETRTDPELEK EAEGS

Genular Protein ID: 885740959

Symbol: Q8N2W7_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 413
  • Mass: 43822
  • Checksum: FCED20584BEE0E06
  • Sequence:
  • VLPPVKSQAA GHAWLSLDTH CHLHYEVLLA GLGGSEQGTV TAHLLGPPGT PGPRRLLKGF 
    YGSEAQGVVK DLEPELLRHL AKGMASLMIT TKGSPRGELR GQVHIANQCE VGGLRLEAAG 
    AEGVRALGAP DTASAAPPVV PGLPALAPAK PGGPGRPRDP NTCFFEGQQR PHGARWAPNY 
    DPLCSLCTCQ RRTVICDPVV CPPPSCPHPV QAPDQCCPVC PEKQDVRDLP GLPRSRDPGE 
    GCYFDGDRSW RAAGTRWHPV VPPFGLIKCA VCTCKGGTGE VHCEKVQCPR LACAQPVRVN 
    PTDCCKQCPV GSGAHPQLGD PMQADGPRGC RFAGQWFPES QSWHPSVPPF GEMSCITCRC 
    GAGVPHCERD DCSLPLSCGS GKESRCCSRC TAHRRPAPET RTDPELEKEA EGS

Genular Protein ID: 1587742171

Symbol: E7ESX1_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 16641997

Title: The DNA sequence, annotation and analysis of human chromosome 3.

PubMed ID: 16641997

DOI: 10.1038/nature04728

Sequence Information:

  • Length: 954
  • Mass: 101961
  • Checksum: 557AC50B00D5AF14
  • Sequence:
  • MPSLPAPPAP LLLLGLLLLG SRPARGAGPE PPVLPIRSEK EPLPVRGAAG CTFGGKVYAL 
    DETWHPDLGE PFGVMRCVLC ACEAPQWGRR TRGPGRVSCK NIKPECPTPA CGQPRQLPGH 
    CCQTCPQERS SSERQPSGLS FEYPRDPEHR SYSDRGEPGA EERARGDGHT DFVALLTGPR 
    SQAVARARVS LLRSSLRFSI SYRRLDRPTR IRFSDSNGSV LFEHPAAPTQ DGLVCGVWRA 
    VPRLSLRLLR AEQLHVALVT LTHPSGEVWG PLIRHRALAA ETFSAILTLE GPPQQGVGGI 
    TLLTLSDTED SLHFLLLFRG LLEPRSGGLT QVPLRLQILH QGQLLRELQA NVSAQEPGFA 
    EVLPNLTVQE MDWLVLGELQ MALEWAGRPG LRISGHIAAR KSCDVLQSVL CGADALIPVQ 
    TGAAGSASLT LLGNGSLIYQ VQVVGTSSEV VAMTLETKPQ RRDQRTVLCH MAGLQPGGHT 
    AVGICPGLGA RGAHMLLQNE LFLNVGTKDF PDGELRGHVA ALPYCGHSAR HDTLPVPLAG 
    ALVLPPVKSQ AAGHAWLSLD THCHLHYEVL LAGLGGSEQG TVTAHLLGPP GTPGPRRLLK 
    GFYGSEAQGV VKDLEPELLR HLAKGMASLM ITTKGSPRGE LRGQVHIANQ CEVGGLRLEA 
    AGAEGVRALG APDTASAAPP VVPGLPALAP AKPGGPGRPR DPNTCFFEGQ QRPHGARWAP 
    NYDPLCSLCT CQRRTVICDP VVCPPPSCPH PVQAPDQCCP VCPEKQDVRD LPGLPRSRDP 
    GEGCYFDGDR SWRAAGTRWH PVVPPFGLIK CAVCTCKGGT GEVHCEKVQC PRLACAQPVR 
    VNPTDCCKQC PVGSGAHPQL GDPMQADGPR GCRFAGQWFP ESQSWHPSVP PFGEMSCITC 
    RCGAGVPHCE RDDCSLPLSC GSGKESRCCS RCTAHRRPPE TRTDPELEKE AEGS

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.