Details for: F11

Gene ID: 2160

Symbol: F11

Ensembl ID: ENSG00000088926

Description: coagulation factor XI

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: centrilobular region hepatocyte (CL0019029)
    Fold Change: 1.5239
    Cell Significance Index: 25.6700
  • Cell Name: epithelial cell of exocrine pancreas (CL1001433)
    Fold Change: 1.1549
    Cell Significance Index: 0.5800
  • Cell Name: CD14-low, CD16-positive monocyte (CL0002396)
    Fold Change: 0.9601
    Cell Significance Index: 23.2600
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.5744
    Cell Significance Index: 16.5500
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.5663
    Cell Significance Index: 107.7800
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.5251
    Cell Significance Index: 104.2100
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: 0.4082
    Cell Significance Index: 13.0800
  • Cell Name: liver dendritic cell (CL2000055)
    Fold Change: 0.3829
    Cell Significance Index: 1.0100
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.3473
    Cell Significance Index: 20.8500
  • Cell Name: kidney epithelial cell (CL0002518)
    Fold Change: 0.3096
    Cell Significance Index: 9.1200
  • Cell Name: precursor cell (CL0011115)
    Fold Change: 0.2651
    Cell Significance Index: 2.0100
  • Cell Name: intrahepatic cholangiocyte (CL0002538)
    Fold Change: 0.2509
    Cell Significance Index: 0.9500
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: 0.2109
    Cell Significance Index: 4.5700
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.2061
    Cell Significance Index: 22.4200
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.2038
    Cell Significance Index: 183.9800
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.1887
    Cell Significance Index: 18.6700
  • Cell Name: midzonal region hepatocyte (CL0019028)
    Fold Change: 0.1624
    Cell Significance Index: 0.9400
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.1244
    Cell Significance Index: 8.6100
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.1078
    Cell Significance Index: 17.5400
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: 0.0850
    Cell Significance Index: 12.3600
  • Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
    Fold Change: 0.0772
    Cell Significance Index: 1.1100
  • Cell Name: periportal region hepatocyte (CL0019026)
    Fold Change: 0.0684
    Cell Significance Index: 1.0100
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: 0.0651
    Cell Significance Index: 11.1100
  • Cell Name: hepatoblast (CL0005026)
    Fold Change: 0.0612
    Cell Significance Index: 1.0300
  • Cell Name: BEST4+ enteroycte (CL4030026)
    Fold Change: 0.0352
    Cell Significance Index: 0.5300
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: 0.0338
    Cell Significance Index: 0.7200
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: 0.0247
    Cell Significance Index: 18.1400
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: 0.0222
    Cell Significance Index: 6.3800
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.0205
    Cell Significance Index: 4.1200
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: 0.0179
    Cell Significance Index: 0.6300
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: 0.0173
    Cell Significance Index: 2.0200
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0164
    Cell Significance Index: 25.2400
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.0121
    Cell Significance Index: 0.5500
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: 0.0120
    Cell Significance Index: 1.3800
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: 0.0114
    Cell Significance Index: 0.7200
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 0.0104
    Cell Significance Index: 0.2600
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 0.0068
    Cell Significance Index: 4.6800
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: 0.0048
    Cell Significance Index: 3.6200
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: 0.0040
    Cell Significance Index: 0.2500
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.0028
    Cell Significance Index: 5.2200
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 0.0022
    Cell Significance Index: 1.4000
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0015
    Cell Significance Index: 2.8700
  • Cell Name: cytotoxic T cell (CL0000910)
    Fold Change: 0.0014
    Cell Significance Index: 0.0200
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0003
    Cell Significance Index: 0.3700
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: -0.0005
    Cell Significance Index: -0.1800
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0017
    Cell Significance Index: -0.9800
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0017
    Cell Significance Index: -1.2800
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0029
    Cell Significance Index: -1.8000
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: -0.0032
    Cell Significance Index: -1.7400
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0033
    Cell Significance Index: -1.5000
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: -0.0038
    Cell Significance Index: -0.1700
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: -0.0049
    Cell Significance Index: -0.3800
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: -0.0061
    Cell Significance Index: -0.4100
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: -0.0065
    Cell Significance Index: -0.2500
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.0071
    Cell Significance Index: -1.4900
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: -0.0099
    Cell Significance Index: -1.7800
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.0121
    Cell Significance Index: -0.2600
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: -0.0126
    Cell Significance Index: -1.7300
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: -0.0148
    Cell Significance Index: -1.8200
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.0160
    Cell Significance Index: -1.6700
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.0172
    Cell Significance Index: -1.7600
  • Cell Name: kidney loop of Henle thick ascending limb epithelial cell (CL1001106)
    Fold Change: -0.0211
    Cell Significance Index: -0.1900
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.0221
    Cell Significance Index: -1.7500
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.0221
    Cell Significance Index: -0.6300
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -0.0225
    Cell Significance Index: -1.1700
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.0267
    Cell Significance Index: -1.5000
  • Cell Name: cholangiocyte (CL1000488)
    Fold Change: -0.0274
    Cell Significance Index: -0.2700
  • Cell Name: keratocyte (CL0002363)
    Fold Change: -0.0274
    Cell Significance Index: -0.4400
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.0280
    Cell Significance Index: -1.7200
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: -0.0280
    Cell Significance Index: -0.7500
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.0326
    Cell Significance Index: -1.5300
  • Cell Name: epithelial cell of proximal tubule (CL0002306)
    Fold Change: -0.0327
    Cell Significance Index: -0.2500
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.0394
    Cell Significance Index: -1.3800
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.0396
    Cell Significance Index: -1.2600
  • Cell Name: fibro/adipogenic progenitor cell (CL0009099)
    Fold Change: -0.0399
    Cell Significance Index: -2.0100
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.0409
    Cell Significance Index: -2.1300
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: -0.0414
    Cell Significance Index: -1.1600
  • Cell Name: neuron associated cell (CL0000095)
    Fold Change: -0.0416
    Cell Significance Index: -1.7100
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.0422
    Cell Significance Index: -1.0900
  • Cell Name: type I muscle cell (CL0002211)
    Fold Change: -0.0443
    Cell Significance Index: -1.0800
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.0455
    Cell Significance Index: -1.4900
  • Cell Name: peg cell (CL4033014)
    Fold Change: -0.0463
    Cell Significance Index: -1.0700
  • Cell Name: lens fiber cell (CL0011004)
    Fold Change: -0.0482
    Cell Significance Index: -1.5300
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: -0.0496
    Cell Significance Index: -0.8500
  • Cell Name: hepatocyte (CL0000182)
    Fold Change: -0.0498
    Cell Significance Index: -0.6900
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -0.0499
    Cell Significance Index: -1.8300
  • Cell Name: hippocampal astrocyte (CL0002604)
    Fold Change: -0.0501
    Cell Significance Index: -0.7000
  • Cell Name: corneal epithelial cell (CL0000575)
    Fold Change: -0.0506
    Cell Significance Index: -0.7200
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: -0.0516
    Cell Significance Index: -1.4800
  • Cell Name: fast muscle cell (CL0000190)
    Fold Change: -0.0527
    Cell Significance Index: -0.6900
  • Cell Name: astrocyte of the cerebral cortex (CL0002605)
    Fold Change: -0.0555
    Cell Significance Index: -0.9600
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: -0.0558
    Cell Significance Index: -1.0900
  • Cell Name: basal cell of epidermis (CL0002187)
    Fold Change: -0.0585
    Cell Significance Index: -0.8900
  • Cell Name: neuron (CL0000540)
    Fold Change: -0.0591
    Cell Significance Index: -0.5600
  • Cell Name: CD4-positive, alpha-beta thymocyte (CL0000810)
    Fold Change: -0.0603
    Cell Significance Index: -1.0400
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: -0.0616
    Cell Significance Index: -0.9100
  • Cell Name: pulmonary alveolar type 2 cell (CL0002063)
    Fold Change: -0.0629
    Cell Significance Index: -0.5200
  • Cell Name: near-projecting glutamatergic cortical neuron (CL4023012)
    Fold Change: -0.0629
    Cell Significance Index: -1.5700
  • Cell Name: regular ventricular cardiac myocyte (CL0002131)
    Fold Change: -0.0643
    Cell Significance Index: -0.8300
  • Cell Name: epithelial cell of pancreas (CL0000083)
    Fold Change: -0.0646
    Cell Significance Index: -1.0700

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. **Serine-type protease**: F11 is a serine-type protease, which means it requires a serine residue at its active site to catalyze the conversion of substrate to product. 2. **Intrinsic pathway of fibrin clot formation**: F11 is activated by thrombin and factor XIa, leading to the activation of the coagulation cascade and the formation of a fibrin clot. 3. **Hemostasis**: F11 plays a critical role in hemostasis, the process of stopping bleeding after an injury. 4. **Hemophilia B**: Deficiencies in F11 are associated with Hemophilia B, a severe bleeding disorder characterized by prolonged bleeding episodes. **Pathways and Functions:** 1. **Blood coagulation pathway**: F11 is involved in the intrinsic pathway of fibrin clot formation, where it is activated by thrombin and factor XIa, leading to the conversion of factor XII to XIIa. 2. **Contact activation system (CAS)**: F11 is also involved in the contact activation system, where it is activated by the interaction of blood components with the endothelial surface. 3. **Kallikrein/kinin system (KKS)**: F11 is involved in the kallikrein/kinin system, where it is activated by the interaction of kininogen with kallikrein. 4. **Fibrinolysis**: F11 is also involved in the regulation of fibrinolysis, the process of dissolving fibrin clots. **Clinical Significance:** 1. **Hemophilia B**: Deficiencies in F11 are associated with Hemophilia B, a severe bleeding disorder characterized by prolonged bleeding episodes. 2. **Thrombosis**: F11 is also involved in the formation of thrombi, which can lead to cardiovascular disease. 3. **Cancer progression**: F11 is implicated in the progression of various cancers, including breast and lung cancer. 4. **Inflammation**: F11 is also involved in the regulation of inflammation, which can lead to various diseases, including atherosclerosis and arthritis. In conclusion, coagulation factor XI is a critical protein involved in the blood coagulation cascade, playing a pivotal role in hemostasis and disease. Its involvement in various pathological processes, including cancer progression and inflammation, highlights the importance of further research into the functions and clinical significance of F11.

Genular Protein ID: 999734601

Symbol: FA11_HUMAN

Name: Coagulation factor XI

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 3636155

Title: Amino acid sequence of human factor XI, a blood coagulation factor with four tandem repeats that are highly homologous with plasma prekallikrein.

PubMed ID: 3636155

DOI: 10.1021/bi00357a018

PubMed ID: 2827746

Title: Organization of the gene for human factor XI.

PubMed ID: 2827746

DOI: 10.1021/bi00397a004

PubMed ID: 9593722

Title: Molecular cloning of platelet factor XI, an alternative splicing product of the plasma factor XI gene.

PubMed ID: 9593722

DOI: 10.1074/jbc.273.22.13787

PubMed ID: 15815621

Title: Generation and annotation of the DNA sequences of human chromosomes 2 and 4.

PubMed ID: 15815621

DOI: 10.1038/nature03466

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: 1998667

Title: Location of the disulfide bonds in human coagulation factor XI: the presence of tandem apple domains.

PubMed ID: 1998667

DOI: 10.1021/bi00222a008

PubMed ID: 2844223

Title: Inactivation of human plasma kallikrein and factor XIa by protein C inhibitor.

PubMed ID: 2844223

DOI: 10.1021/bi00412a005

PubMed ID: 11412111

Title: Localization of a heparin binding site in the catalytic domain of factor XIa.

PubMed ID: 11412111

DOI: 10.1021/bi0027433

PubMed ID: 16335952

Title: Human plasma N-glycoproteome analysis by immunoaffinity subtraction, hydrazide chemistry, and mass spectrometry.

PubMed ID: 16335952

DOI: 10.1021/pr0502065

PubMed ID: 19159218

Title: Glycoproteomics analysis of human liver tissue by combination of multiple enzyme digestion and hydrazide chemistry.

PubMed ID: 19159218

DOI: 10.1021/pr8008012

PubMed ID: 25092234

Title: Site-specific N-glycosylation analysis of human factor XI: Identification of a noncanonical NXC glycosite.

PubMed ID: 25092234

DOI: 10.1002/pmic.201400038

PubMed ID: 35460690

Title: Novel salivary antihemostatic activities of long-form D7 proteins from the malaria vector Anopheles gambiae facilitate hematophagy.

PubMed ID: 35460690

DOI: 10.1016/j.jbc.2022.101971

PubMed ID: 18510371

Title: Clavatadine A, a natural product with selective recognition and irreversible inhibition of factor XIa.

PubMed ID: 18510371

DOI: 10.1021/jm800314b

PubMed ID: 2813350

Title: Factor XI (plasma thromboplastin antecedent) deficiency in Ashkenazi Jews is a bleeding disorder that can result from three types of point mutations.

PubMed ID: 2813350

DOI: 10.1073/pnas.86.20.7667

PubMed ID: 1547342

Title: Expression of human blood coagulation factor XI: characterization of the defect in factor XI type III deficiency.

PubMed ID: 1547342

PubMed ID: 7888672

Title: Six point mutations that cause factor XI deficiency.

PubMed ID: 7888672

PubMed ID: 7669672

Title: Identification of two novel mutations in non-Jewish factor XI deficiency.

PubMed ID: 7669672

DOI: 10.1111/j.1365-2141.1995.tb05215.x

PubMed ID: 9401068

Title: Severe factor XI deficiency in an Arab family associated with a novel mutation in exon 11.

PubMed ID: 9401068

DOI: 10.1046/j.1365-2141.1997.4343244.x

PubMed ID: 9787168

Title: Identification of mutations and polymorphisms in the factor XI genes of an African American family by dideoxyfingerprinting.

PubMed ID: 9787168

PubMed ID: 10027710

Title: Identification of a novel mutation in a non-Jewish factor XI deficient kindred.

PubMed ID: 10027710

DOI: 10.1046/j.1365-2141.1999.01150.x

PubMed ID: 10606881

Title: Heterozygous factor XI deficiency associated with three novel mutations.

PubMed ID: 10606881

DOI: 10.1046/j.1365-2141.1999.01769.x

PubMed ID: 10391209

Title: Characterization of single-nucleotide polymorphisms in coding regions of human genes.

PubMed ID: 10391209

DOI: 10.1038/10290

PubMed ID: 11895778

Title: Factor XI deficiency in French Basques is caused predominantly by an ancestral Cys38Arg mutation in the factor XI gene.

PubMed ID: 11895778

DOI: 10.1182/blood.v99.7.2448

PubMed ID: 15026311

Title: Dominant factor XI deficiency caused by mutations in the factor XI catalytic domain.

PubMed ID: 15026311

DOI: 10.1182/blood-2003-10-3530

PubMed ID: 15180874

Title: Severe factor XI deficiency caused by compound heterozygosity.

PubMed ID: 15180874

DOI: 10.1111/j.1365-2141.2004.04979.x

PubMed ID: 15953011

Title: Genetic analysis in FXI deficiency: six novel mutations and the use of a polymerase chain reaction-based test to define a whole gene deletion.

PubMed ID: 15953011

DOI: 10.1111/j.1365-2141.2005.05536.x

PubMed ID: 16607084

Title: Identification of five novel mutations in the factor XI gene (F11) of patients with factor XI deficiency.

PubMed ID: 16607084

DOI: 10.1097/01.mbc.0000198054.50257.96

PubMed ID: 18005151

Title: Seven novel point mutations in the F11 gene in Iranian FXI-deficient patients.

PubMed ID: 18005151

DOI: 10.1111/j.1365-2516.2007.01593.x

PubMed ID: 21668437

Title: Population-specific spectrum of the F11 mutations in Koreans: evidence for a founder effect.

PubMed ID: 21668437

DOI: 10.1111/j.1399-0004.2011.01732.x

PubMed ID: 21457405

Title: Three dominant-negative mutations in factor XI-deficient patients.

PubMed ID: 21457405

DOI: 10.1111/j.1365-2516.2011.02519.x

PubMed ID: 22016685

Title: A novel missense mutation Asp506Gly in exon 13 of the F11 gene in an asymptomatic Korean woman with mild factor XI deficiency.

PubMed ID: 22016685

DOI: 10.3343/kjlm.2011.31.4.290

PubMed ID: 22322133

Title: Identification of a novel F11 missense mutation (Ile463Ser) in a family with congenital factor XI deficiency.

PubMed ID: 22322133

DOI: 10.1097/mbc.0b013e32834ea02a

PubMed ID: 21999818

Title: A cluster of factor XI-deficient patients due to a new mutation (Ile 436 Lys) in northeastern Italy.

PubMed ID: 21999818

DOI: 10.1111/j.1600-0609.2011.01723.x

PubMed ID: 22159456

Title: Revisiting the molecular epidemiology of factor XI deficiency: nine new mutations and an original large 4qTer deletion in western Brittany (France).

PubMed ID: 22159456

DOI: 10.1160/th11-06-0415

PubMed ID: 25158988

Title: Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families.

PubMed ID: 25158988

DOI: 10.1097/mbc.0000000000000185

Sequence Information:

  • Length: 625
  • Mass: 70109
  • Checksum: 147AFA94B7709E8F
  • Sequence:
  • MIFLYQVVHF ILFTSVSGEC VTQLLKDTCF EGGDITTVFT PSAKYCQVVC TYHPRCLLFT 
    FTAESPSEDP TRWFTCVLKD SVTETLPRVN RTAAISGYSF KQCSHQISAC NKDIYVDLDM 
    KGINYNSSVA KSAQECQERC TDDVHCHFFT YATRQFPSLE HRNICLLKHT QTGTPTRITK 
    LDKVVSGFSL KSCALSNLAC IRDIFPNTVF ADSNIDSVMA PDAFVCGRIC THHPGCLFFT 
    FFSQEWPKES QRNLCLLKTS ESGLPSTRIK KSKALSGFSL QSCRHSIPVF CHSSFYHDTD 
    FLGEELDIVA AKSHEACQKL CTNAVRCQFF TYTPAQASCN EGKGKCYLKL SSNGSPTKIL 
    HGRGGISGYT LRLCKMDNEC TTKIKPRIVG GTASVRGEWP WQVTLHTTSP TQRHLCGGSI 
    IGNQWILTAA HCFYGVESPK ILRVYSGILN QSEIKEDTSF FGVQEIIIHD QYKMAESGYD 
    IALLKLETTV NYTDSQRPIC LPSKGDRNVI YTDCWVTGWG YRKLRDKIQN TLQKAKIPLV 
    TNEECQKRYR GHKITHKMIC AGYREGGKDA CKGDSGGPLS CKHNEVWHLV GITSWGEGCA 
    QRERPGVYTN VVEYVDWILE KTQAV

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.