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: polychromatophilic erythroblast (CL0000550)
Fold Change: 184.8980
Cell Significance Index: -28.7600 - Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
Fold Change: 113.5058
Cell Significance Index: -28.7900 - Cell Name: embryonic stem cell (CL0002322)
Fold Change: 71.2469
Cell Significance Index: -29.3500 - Cell Name: mucosal type mast cell (CL0000485)
Fold Change: 63.3835
Cell Significance Index: -25.7500 - Cell Name: smooth muscle fiber of ileum (CL1000278)
Fold Change: 61.5306
Cell Significance Index: -29.0500 - Cell Name: peripheral blood mononuclear cell (CL2000001)
Fold Change: 57.3111
Cell Significance Index: -29.4800 - Cell Name: ileal goblet cell (CL1000326)
Fold Change: 43.4561
Cell Significance Index: -29.1600 - Cell Name: ciliated cell of the bronchus (CL0002332)
Fold Change: 26.8973
Cell Significance Index: -25.6800 - Cell Name: orthochromatic erythroblast (CL0000552)
Fold Change: 23.3504
Cell Significance Index: -28.7900 - Cell Name: epidermal Langerhans cell (CL0002457)
Fold Change: 8.2976
Cell Significance Index: -18.1600 - Cell Name: stromal cell of bone marrow (CL0010001)
Fold Change: 7.2807
Cell Significance Index: -28.7300 - Cell Name: centrilobular region hepatocyte (CL0019029)
Fold Change: 5.4791
Cell Significance Index: 92.3000 - Cell Name: decidual cell (CL2000002)
Fold Change: 4.9344
Cell Significance Index: 79.1700 - Cell Name: epithelial cell of pancreas (CL0000083)
Fold Change: 3.5986
Cell Significance Index: 59.3000 - Cell Name: early T lineage precursor (CL0002425)
Fold Change: 2.9118
Cell Significance Index: 42.2800 - Cell Name: leptomeningeal cell (CL0000708)
Fold Change: 2.5901
Cell Significance Index: 55.3700 - Cell Name: colon goblet cell (CL0009039)
Fold Change: 1.9011
Cell Significance Index: 188.0600 - Cell Name: neoplastic cell (CL0001063)
Fold Change: 1.8231
Cell Significance Index: 361.8100 - Cell Name: epithelial cell of small intestine (CL0002254)
Fold Change: 1.7594
Cell Significance Index: 286.1500 - Cell Name: intestinal crypt stem cell of colon (CL0009043)
Fold Change: 1.1746
Cell Significance Index: 127.7600 - Cell Name: proerythroblast (CL0000547)
Fold Change: 1.1633
Cell Significance Index: 16.6700 - Cell Name: gut absorptive cell (CL0000677)
Fold Change: 1.1340
Cell Significance Index: 68.0800 - Cell Name: preadipocyte (CL0002334)
Fold Change: 0.9048
Cell Significance Index: 17.6600 - Cell Name: lung endothelial cell (CL1001567)
Fold Change: 0.8687
Cell Significance Index: 45.2500 - Cell Name: retinal progenitor cell (CL0002672)
Fold Change: 0.7497
Cell Significance Index: 42.0700 - Cell Name: cardiac muscle myoblast (CL0000513)
Fold Change: 0.6424
Cell Significance Index: 49.3000 - Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
Fold Change: 0.6406
Cell Significance Index: 128.5000 - Cell Name: cardiac endothelial cell (CL0010008)
Fold Change: 0.5983
Cell Significance Index: 8.6100 - Cell Name: keratocyte (CL0002363)
Fold Change: 0.5339
Cell Significance Index: 8.4700 - Cell Name: stromal cell of ovary (CL0002132)
Fold Change: 0.5095
Cell Significance Index: 69.9700 - Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
Fold Change: 0.5039
Cell Significance Index: 180.7300 - Cell Name: tuft cell of colon (CL0009041)
Fold Change: 0.4129
Cell Significance Index: 372.8000 - Cell Name: microfold cell of epithelium of small intestine (CL1000353)
Fold Change: 0.3645
Cell Significance Index: 25.2100 - Cell Name: enterocyte of epithelium of large intestine (CL0002071)
Fold Change: 0.2934
Cell Significance Index: 13.3000 - Cell Name: endothelial cell of venule (CL1000414)
Fold Change: 0.2711
Cell Significance Index: 3.0800 - Cell Name: fibro/adipogenic progenitor cell (CL0009099)
Fold Change: 0.2442
Cell Significance Index: 12.3400 - Cell Name: fibroblast of cardiac tissue (CL0002548)
Fold Change: 0.1892
Cell Significance Index: 2.7200 - Cell Name: fibroblast of mammary gland (CL0002555)
Fold Change: 0.1507
Cell Significance Index: 4.3200 - Cell Name: pigmented epithelial cell (CL0000529)
Fold Change: 0.1457
Cell Significance Index: 274.2500 - Cell Name: enteroendocrine cell of small intestine (CL0009006)
Fold Change: 0.1400
Cell Significance Index: 3.5000 - Cell Name: enterocyte of epithelium of small intestine (CL1000334)
Fold Change: 0.1239
Cell Significance Index: 3.5700 - Cell Name: forebrain neuroblast (CL1000042)
Fold Change: 0.1230
Cell Significance Index: 7.5600 - Cell Name: enteroendocrine cell of colon (CL0009042)
Fold Change: 0.1181
Cell Significance Index: 22.4800 - Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
Fold Change: 0.1175
Cell Significance Index: 74.6000 - Cell Name: periportal region hepatocyte (CL0019026)
Fold Change: 0.1091
Cell Significance Index: 1.6100 - Cell Name: paneth cell of epithelium of small intestine (CL1000343)
Fold Change: 0.1006
Cell Significance Index: 2.1800 - Cell Name: ciliary muscle cell (CL1000443)
Fold Change: 0.0916
Cell Significance Index: 41.5600 - Cell Name: GABAergic interneuron (CL0011005)
Fold Change: 0.0901
Cell Significance Index: 62.3100 - Cell Name: odontoblast (CL0000060)
Fold Change: 0.0756
Cell Significance Index: 9.7000 - Cell Name: Hofbauer cell (CL3000001)
Fold Change: 0.0478
Cell Significance Index: 0.3900 - Cell Name: indirect pathway medium spiny neuron (CL4023029)
Fold Change: 0.0440
Cell Significance Index: 1.9500 - Cell Name: eye photoreceptor cell (CL0000287)
Fold Change: 0.0363
Cell Significance Index: 2.2900 - Cell Name: hair follicular keratinocyte (CL2000092)
Fold Change: 0.0214
Cell Significance Index: 9.4500 - Cell Name: lens epithelial cell (CL0002224)
Fold Change: 0.0206
Cell Significance Index: 31.7900 - Cell Name: small intestine goblet cell (CL1000495)
Fold Change: 0.0134
Cell Significance Index: 0.4700 - Cell Name: pulmonary alveolar epithelial cell (CL0000322)
Fold Change: -0.0003
Cell Significance Index: -0.2300 - Cell Name: secondary lens fiber (CL0002225)
Fold Change: -0.0009
Cell Significance Index: -1.2900 - Cell Name: cell in vitro (CL0001034)
Fold Change: -0.0035
Cell Significance Index: -1.8900 - Cell Name: intermediate cell of urothelium (CL4030055)
Fold Change: -0.0052
Cell Significance Index: -0.9400 - Cell Name: pancreatic PP cell (CL0002275)
Fold Change: -0.0077
Cell Significance Index: -4.8300 - Cell Name: anterior lens cell (CL0002223)
Fold Change: -0.0102
Cell Significance Index: -18.7700 - Cell Name: pancreatic A cell (CL0000171)
Fold Change: -0.0170
Cell Significance Index: -12.6200 - Cell Name: type B pancreatic cell (CL0000169)
Fold Change: -0.0206
Cell Significance Index: -11.6300 - Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
Fold Change: -0.0352
Cell Significance Index: -0.7500 - Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
Fold Change: -0.0377
Cell Significance Index: -27.6500 - Cell Name: dopaminergic neuron (CL0000700)
Fold Change: -0.0694
Cell Significance Index: -19.9600 - Cell Name: hippocampal granule cell (CL0001033)
Fold Change: -0.0739
Cell Significance Index: -4.9700 - Cell Name: pigmented ciliary epithelial cell (CL0002303)
Fold Change: -0.0746
Cell Significance Index: -10.8500 - Cell Name: pancreatic D cell (CL0000173)
Fold Change: -0.0812
Cell Significance Index: -17.1000 - Cell Name: hippocampal pyramidal neuron (CL1001571)
Fold Change: -0.0894
Cell Significance Index: -2.5500 - Cell Name: pancreatic acinar cell (CL0002064)
Fold Change: -0.0968
Cell Significance Index: -16.5300 - Cell Name: epithelial cell of stomach (CL0002178)
Fold Change: -0.1057
Cell Significance Index: -12.3200 - Cell Name: basal cell of urothelium (CL1000486)
Fold Change: -0.1311
Cell Significance Index: -16.1200 - Cell Name: direct pathway medium spiny neuron (CL4023026)
Fold Change: -0.1320
Cell Significance Index: -5.0000 - Cell Name: abnormal cell (CL0001061)
Fold Change: -0.1486
Cell Significance Index: -15.1800 - Cell Name: transit amplifying cell of small intestine (CL0009012)
Fold Change: -0.1509
Cell Significance Index: -3.1300 - Cell Name: pancreatic ductal cell (CL0002079)
Fold Change: -0.1828
Cell Significance Index: -20.9400 - Cell Name: lactocyte (CL0002325)
Fold Change: -0.2190
Cell Significance Index: -28.2900 - Cell Name: corneal epithelial cell (CL0000575)
Fold Change: -0.2227
Cell Significance Index: -3.1700 - Cell Name: pancreatic endocrine cell (CL0008024)
Fold Change: -0.2338
Cell Significance Index: -26.6900 - Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
Fold Change: -0.2385
Cell Significance Index: -24.8300 - Cell Name: hepatoblast (CL0005026)
Fold Change: -0.2420
Cell Significance Index: -4.0700 - Cell Name: mesenchymal cell (CL0008019)
Fold Change: -0.2474
Cell Significance Index: -4.1400 - Cell Name: tonsil germinal center B cell (CL2000006)
Fold Change: -0.2545
Cell Significance Index: -30.0100 - Cell Name: transit amplifying cell of colon (CL0009011)
Fold Change: -0.2660
Cell Significance Index: -8.5200 - Cell Name: sebum secreting cell (CL0000317)
Fold Change: -0.2784
Cell Significance Index: -19.6900 - Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
Fold Change: -0.3505
Cell Significance Index: -27.7600 - Cell Name: cardiac muscle cell (CL0000746)
Fold Change: -0.3515
Cell Significance Index: -5.1900 - Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
Fold Change: -0.3528
Cell Significance Index: -16.5800 - Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
Fold Change: -0.3781
Cell Significance Index: -28.1800 - Cell Name: cortical interneuron (CL0008031)
Fold Change: -0.3959
Cell Significance Index: -9.5000 - Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
Fold Change: -0.4129
Cell Significance Index: -11.5400 - Cell Name: BEST4+ enteroycte (CL4030026)
Fold Change: -0.4207
Cell Significance Index: -6.3400 - Cell Name: granulosa cell (CL0000501)
Fold Change: -0.4347
Cell Significance Index: -11.4300 - Cell Name: early pro-B cell (CL0002046)
Fold Change: -0.4638
Cell Significance Index: -29.9200 - Cell Name: vascular lymphangioblast (CL0005022)
Fold Change: -0.4669
Cell Significance Index: -8.2500 - Cell Name: intestinal tuft cell (CL0019032)
Fold Change: -0.4872
Cell Significance Index: -29.8700 - Cell Name: endothelial cell of placenta (CL0009092)
Fold Change: -0.4982
Cell Significance Index: -3.0100 - Cell Name: glycinergic neuron (CL1001509)
Fold Change: -0.5203
Cell Significance Index: -27.3200 - Cell Name: bladder urothelial cell (CL1001428)
Fold Change: -0.5261
Cell Significance Index: -27.3300
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.
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.
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
Genular Protein ID: 764541020
Symbol: PROS_HUMAN
Name: Vitamin K-dependent protein S
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 2820795
Title: Human protein S cDNA encodes Phe-16 and Tyr 222 in consensus sequences for the post-translational processing.
PubMed ID: 2820795
PubMed ID: 3467362
Title: Cloning and characterization of human liver cDNA encoding a protein S precursor.
PubMed ID: 3467362
PubMed ID: 2148110
PubMed ID: 2148111
Title: Intron-exon organization of the active human protein S gene PS alpha and its pseudogene PS beta: duplication and silencing during primate evolution.
PubMed ID: 2148111
DOI: 10.1021/bi00486a011
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
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: 2944113
Title: Isolation and sequence of the cDNA for human protein S, a regulator of blood coagulation.
PubMed ID: 2944113
PubMed ID: 7482398
Title: Identification of eight point mutations in protein S deficiency type I -- analysis of 15 pedigrees.
PubMed ID: 7482398
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: 24275569
Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
PubMed ID: 24275569
PubMed ID: 15952784
Title: Solution structure of the Ca2+-binding EGF3-4 pair from vitamin K-dependent protein S: identification of an unusual fold in EGF3.
PubMed ID: 15952784
DOI: 10.1021/bi050101f
PubMed ID: 2143091
Title: Heerlen polymorphism of protein S, an immunologic polymorphism due to dimorphism of residue 460.
PubMed ID: 2143091
PubMed ID: 8298131
Title: Protein S Tokushima: abnormal molecule with a substitution of Glu for Lys-155 in the second epidermal growth factor-like domain of protein S.
PubMed ID: 8298131
PubMed ID: 7803790
Title: Identification of 15 different candidate causal point mutations and three polymorphisms in 19 patients with protein S deficiency using a scanning method for the analysis of the protein S active gene.
PubMed ID: 7803790
PubMed ID: 7545463
Title: Detection and characterization of seven novel protein S (PROS) gene lesions: evaluation of reverse transcript-polymerase chain reaction as a mutation screening strategy.
PubMed ID: 7545463
PubMed ID: 7579449
Title: Protein S deficiency type I: identification of point mutations in 9 of 10 families.
PubMed ID: 7579449
PubMed ID: 8977443
Title: Identification of two novel point mutations in the human protein S gene associated with familial protein S deficiency and thrombosis.
PubMed ID: 8977443
PubMed ID: 8639833
Title: Molecular basis of a hereditary type I protein S deficiency caused by a substitution of Cys for Arg474.
PubMed ID: 8639833
PubMed ID: 8781426
Title: Molecular basis of protein S deficiency in three families also showing independent inheritance of factor V Leiden.
PubMed ID: 8781426
PubMed ID: 8943854
Title: Identification of 19 protein S gene mutations in patients with phenotypic protein S deficiency and thrombosis.
PubMed ID: 8943854
PubMed ID: 8765219
Title: Molecular basis for protein S hereditary deficiency: genetic defects observed in 118 patients with type I and type IIa deficiencies.
PubMed ID: 8765219
PubMed ID: 8701404
Title: Five novel mutations of the protein S active gene (PROS 1) in 8 Norman families.
PubMed ID: 8701404
PubMed ID: 9031443
Title: Identification of three novel mutations in hereditary protein S deficiency.
PubMed ID: 9031443
PubMed ID: 9241758
Title: Protein S deficiency: a database of mutations.
PubMed ID: 9241758
PubMed ID: 10447256
Title: Protein S gene analysis reveals the presence of a cosegregating mutation in most pedigrees with type I but not type III PS deficiency.
PubMed ID: 10447256
DOI: 10.1002/(sici)1098-1004(1999)14:1<30::aid-humu4>3.0.co;2-x
PubMed ID: 10613647
Title: Poor relationship between phenotypes of protein S deficiency and mutations in the protein S alpha gene.
PubMed ID: 10613647
PubMed ID: 10706858
Title: Genetic analysis, phenotypic diagnosis, and risk of venous thrombosis in families with inherited deficiencies of protein S.
PubMed ID: 10706858
PubMed ID: 10790208
Title: Optimization of a simple and rapid single-strand conformation analysis for detection of mutations in the PROS1 gene: identification of seven novel mutations and three novel, apparently neutral, variants.
PubMed ID: 10790208
DOI: 10.1002/(sici)1098-1004(200005)15:5<463::aid-humu8>3.0.co;2-e
PubMed ID: 11372770
Title: DNA sequence analysis of protein S deficiency -- identification of four point mutations in twelve Japanese subjects.
PubMed ID: 11372770
DOI: 10.1055/s-2001-14075
PubMed ID: 11776305
Title: Characterization and structural impact of five novel PROS1 mutations in eleven protein S-deficient families.
PubMed ID: 11776305
PubMed ID: 12351389
Title: Protein S Gla-domain mutations causing impaired Ca(2+)-induced phospholipid binding and severe functional protein S deficiency.
PubMed ID: 12351389
PubMed ID: 11858485
Title: Genetic and phenotypic variability between families with hereditary protein S deficiency.
PubMed ID: 11858485
PubMed ID: 11927129
Title: Four missense mutations identified in the protein S gene of thrombosis patients with protein S deficiency: effects on secretion and anticoagulant activity of protein S.
PubMed ID: 11927129
PubMed ID: 12632031
Title: Familial thrombophilia is an oligogenetic disease: involvement of the prothrombin G20210A, PROC and PROS gene mutations.
PubMed ID: 12632031
PubMed ID: 15238143
Title: Identification of protein Salpha gene mutations including four novel mutations in eight unrelated patients with protein S deficiency.
PubMed ID: 15238143
PubMed ID: 15712227
Title: Molecular diversity and thrombotic risk in protein S deficiency: the PROSIT study.
PubMed ID: 15712227
DOI: 10.1002/humu.20136
PubMed ID: 16959974
Title: The consensus coding sequences of human breast and colorectal cancers.
PubMed ID: 16959974
PubMed ID: 18322254
Title: Functional characterization of twelve natural PROS1 mutations associated with anticoagulant protein S deficiency.
PubMed ID: 18322254
PubMed ID: 20484936
Title: Intracerebral mass bleeding in a term neonate: manifestation of hereditary protein S deficiency with a new mutation in the PROS1 gene.
PubMed ID: 20484936
DOI: 10.1159/000298282
PubMed ID: 27535533
Title: Analysis of protein-coding genetic variation in 60,706 humans.
PubMed ID: 27535533
DOI: 10.1038/nature19057
Sequence Information:
- Length: 676
- Mass: 75123
- Checksum: 2B88A04F85403F25
- Sequence:
MRVLGGRCGA LLACLLLVLP VSEANFLSKQ QASQVLVRKR RANSLLEETK QGNLERECIE ELCNKEEARE VFENDPETDY FYPKYLVCLR SFQTGLFTAA RQSTNAYPDL RSCVNAIPDQ CSPLPCNEDG YMSCKDGKAS FTCTCKPGWQ GEKCEFDINE CKDPSNINGG CSQICDNTPG SYHCSCKNGF VMLSNKKDCK DVDECSLKPS ICGTAVCKNI PGDFECECPE GYRYNLKSKS CEDIDECSEN MCAQLCVNYP GGYTCYCDGK KGFKLAQDQK SCEVVSVCLP LNLDTKYELL YLAEQFAGVV LYLKFRLPEI SRFSAEFDFR TYDSEGVILY AESIDHSAWL LIALRGGKIE VQLKNEHTSK ITTGGDVINN GLWNMVSVEE LEHSISIKIA KEAVMDINKP GPLFKPENGL LETKVYFAGF PRKVESELIK PINPRLDGCI RSWNLMKQGA SGIKEIIQEK QNKHCLVTVE KGSYYPGSGI AQFHIDYNNV SSAEGWHVNV TLNIRPSTGT GVMLALVSGN NTVPFAVSLV DSTSEKSQDI LLSVENTVIY RIQALSLCSD QQSHLEFRVN RNNLELSTPL KIETISHEDL QRQLAVLDKA MKAKVATYLG GLPDVPFSAT PVNAFYNGCM EVNINGVQLD LDEAISKHND IRAHSCPSVW KKTKNS
Genular Protein ID: 3927980759
Symbol: A0A0S2Z4L3_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
PubMed ID: 24275569
Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.
PubMed ID: 24275569
PubMed ID: 26871637
Title: Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.
PubMed ID: 26871637
Sequence Information:
- Length: 708
- Mass: 78854
- Checksum: 7019A63DD3043AB2
- Sequence:
MRVLGGRCGA LLACLLLVLP VSEANFCLYF RNDFIYNRAC ISVLVGLSGC NFFYSICFLS KQQASQVLVR KRRANSLLEE TKQGNLEREC IEELCNKEEA REVFENDPET DYFYPKYLVC LRSFQTGLFT AARQSTNAYP DLRSCVNAIP DQCSPLPCNE DGYMSCKDGK ASFTCTCKPG WQGEKCEFDI NECKDPSNIN GGCSQICDNT PGSYHCSCKN GFVMLSNKKD CKDVDECSLK PSICGTAVCK NIPGDFECEC PEGYRYNLKS KSCEDIDECS ENMCAQLCVN YPGGYTCYCD GKKGFKLAQD QKSCEVVSVC LPLNLDTKYE LLYLAEQFAG VVLYLKFRLP EISRFSAEFD FRTYDSEGVI LYAESIDHSA WLLIALRGGK IEVQLKNEHT SKITTGGDVI NNGLWNMVSV EELEHSISIK IAKEAVMDIN KPGPLFKPEN GLLETKVYFA GFPRKVESEL IKPINPRLDG CIRSWNLMKQ GASGIKEIIQ EKQNKHCLVT VEKGSYYPGS GIAQFHIDYN NVSSAEGWHV NVTLNIRPST GTGVMLALVS GNNTVPFAVS LVDSTSEKSQ DILLSVENTV IYRIQALSLC SDQQSHLEFR VNRNNLELST PLKIETISHE DLQRQLAVLD KAMKAKVATY LGGLPDVPFS ATPVNAFYNG CMEVNINGVQ LDLDEAISKH NDIRAHSCPS VWKKTKNS
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.