Details for: WRN
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: 229.5152
Cell Significance Index: -35.7000 - Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
Fold Change: 157.7806
Cell Significance Index: -40.0200 - Cell Name: mucosal type mast cell (CL0000485)
Fold Change: 83.9616
Cell Significance Index: -34.1100 - Cell Name: ciliated cell of the bronchus (CL0002332)
Fold Change: 35.9626
Cell Significance Index: -34.3400 - Cell Name: orthochromatic erythroblast (CL0000552)
Fold Change: 32.9614
Cell Significance Index: -40.6400 - Cell Name: CD8-alpha-beta-positive, alpha-beta intraepithelial T cell (CL0000796)
Fold Change: 14.8907
Cell Significance Index: -39.8900 - Cell Name: CD8-positive, alpha-beta regulatory T cell (CL0000795)
Fold Change: 12.3394
Cell Significance Index: -37.9000 - Cell Name: epidermal Langerhans cell (CL0002457)
Fold Change: 10.9477
Cell Significance Index: -23.9600 - Cell Name: stromal cell of bone marrow (CL0010001)
Fold Change: 10.5802
Cell Significance Index: -41.7500 - Cell Name: retinal progenitor cell (CL0002672)
Fold Change: 3.0028
Cell Significance Index: 168.5000 - Cell Name: neoplastic cell (CL0001063)
Fold Change: 2.3426
Cell Significance Index: 464.9000 - Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
Fold Change: 1.8868
Cell Significance Index: 378.5000 - Cell Name: preadipocyte (CL0002334)
Fold Change: 1.6145
Cell Significance Index: 31.5100 - Cell Name: tuft cell of colon (CL0009041)
Fold Change: 1.5601
Cell Significance Index: 1408.6800 - Cell Name: forebrain neuroblast (CL1000042)
Fold Change: 1.3105
Cell Significance Index: 80.5500 - Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
Fold Change: 1.2234
Cell Significance Index: 34.1900 - Cell Name: intestinal crypt stem cell of colon (CL0009043)
Fold Change: 1.1032
Cell Significance Index: 120.0000 - Cell Name: direct pathway medium spiny neuron (CL4023026)
Fold Change: 1.0258
Cell Significance Index: 38.8500 - Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
Fold Change: 1.0029
Cell Significance Index: 359.7100 - Cell Name: cortical interneuron (CL0008031)
Fold Change: 0.9953
Cell Significance Index: 23.8700 - Cell Name: indirect pathway medium spiny neuron (CL4023029)
Fold Change: 0.9515
Cell Significance Index: 42.0900 - Cell Name: cardiac muscle myoblast (CL0000513)
Fold Change: 0.9072
Cell Significance Index: 69.6200 - Cell Name: gut absorptive cell (CL0000677)
Fold Change: 0.8787
Cell Significance Index: 52.7600 - Cell Name: enterocyte of epithelium of small intestine (CL1000334)
Fold Change: 0.8644
Cell Significance Index: 24.9100 - Cell Name: GABAergic interneuron (CL0011005)
Fold Change: 0.8555
Cell Significance Index: 591.6700 - Cell Name: lung endothelial cell (CL1001567)
Fold Change: 0.8331
Cell Significance Index: 43.4000 - Cell Name: enteroendocrine cell of small intestine (CL0009006)
Fold Change: 0.8005
Cell Significance Index: 20.0100 - Cell Name: conjunctival epithelial cell (CL1000432)
Fold Change: 0.7535
Cell Significance Index: 10.2800 - Cell Name: skeletal muscle fiber (CL0008002)
Fold Change: 0.7242
Cell Significance Index: 18.6200 - Cell Name: basal epithelial cell of prostatic duct (CL0002236)
Fold Change: 0.7120
Cell Significance Index: 6.3200 - Cell Name: hippocampal granule cell (CL0001033)
Fold Change: 0.6152
Cell Significance Index: 41.3700 - Cell Name: enterocyte of epithelium of large intestine (CL0002071)
Fold Change: 0.5743
Cell Significance Index: 26.0300 - Cell Name: epithelial cell of stomach (CL0002178)
Fold Change: 0.5735
Cell Significance Index: 66.8300 - Cell Name: intermediate cell of urothelium (CL4030055)
Fold Change: 0.4953
Cell Significance Index: 89.3000 - Cell Name: microfold cell of epithelium of small intestine (CL1000353)
Fold Change: 0.4825
Cell Significance Index: 33.3700 - Cell Name: basal cell of urothelium (CL1000486)
Fold Change: 0.3933
Cell Significance Index: 48.3700 - Cell Name: small intestine goblet cell (CL1000495)
Fold Change: 0.3816
Cell Significance Index: 13.4100 - Cell Name: colon goblet cell (CL0009039)
Fold Change: 0.3558
Cell Significance Index: 35.2000 - Cell Name: paneth cell of epithelium of small intestine (CL1000343)
Fold Change: 0.3487
Cell Significance Index: 7.5600 - Cell Name: leptomeningeal cell (CL0000708)
Fold Change: 0.3312
Cell Significance Index: 7.0800 - Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
Fold Change: 0.2998
Cell Significance Index: 14.0900 - Cell Name: stromal cell of ovary (CL0002132)
Fold Change: 0.2731
Cell Significance Index: 37.5100 - Cell Name: hair follicular keratinocyte (CL2000092)
Fold Change: 0.2389
Cell Significance Index: 105.6100 - Cell Name: pigmented epithelial cell (CL0000529)
Fold Change: 0.2353
Cell Significance Index: 442.9900 - Cell Name: lens epithelial cell (CL0002224)
Fold Change: 0.2342
Cell Significance Index: 360.6200 - Cell Name: anterior lens cell (CL0002223)
Fold Change: 0.2264
Cell Significance Index: 417.5700 - Cell Name: secondary lens fiber (CL0002225)
Fold Change: 0.2112
Cell Significance Index: 287.1200 - Cell Name: fibroblast of cardiac tissue (CL0002548)
Fold Change: 0.1880
Cell Significance Index: 2.7000 - Cell Name: cortical cell of adrenal gland (CL0002097)
Fold Change: 0.1761
Cell Significance Index: 4.7200 - Cell Name: ciliary muscle cell (CL1000443)
Fold Change: 0.1717
Cell Significance Index: 77.9400 - Cell Name: cell in vitro (CL0001034)
Fold Change: 0.1478
Cell Significance Index: 80.7200 - Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
Fold Change: 0.1466
Cell Significance Index: 93.0900 - Cell Name: acinar cell of salivary gland (CL0002623)
Fold Change: 0.0652
Cell Significance Index: 3.0400 - Cell Name: fibroblast of mammary gland (CL0002555)
Fold Change: 0.0610
Cell Significance Index: 1.7500 - Cell Name: cerebellar granule cell (CL0001031)
Fold Change: 0.0373
Cell Significance Index: 0.6400 - Cell Name: epithelial cell of small intestine (CL0002254)
Fold Change: 0.0060
Cell Significance Index: 0.9800 - Cell Name: pancreatic acinar cell (CL0002064)
Fold Change: -0.0124
Cell Significance Index: -2.1100 - Cell Name: placental villous trophoblast (CL2000060)
Fold Change: -0.0311
Cell Significance Index: -0.8300 - Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
Fold Change: -0.0424
Cell Significance Index: -31.0900 - Cell Name: pancreatic A cell (CL0000171)
Fold Change: -0.0498
Cell Significance Index: -36.8900 - Cell Name: cardiac endothelial cell (CL0010008)
Fold Change: -0.0501
Cell Significance Index: -0.7200 - Cell Name: pulmonary alveolar epithelial cell (CL0000322)
Fold Change: -0.0515
Cell Significance Index: -38.9500 - Cell Name: type B pancreatic cell (CL0000169)
Fold Change: -0.0650
Cell Significance Index: -36.6300 - Cell Name: pancreatic PP cell (CL0002275)
Fold Change: -0.0750
Cell Significance Index: -46.8200 - Cell Name: bladder urothelial cell (CL1001428)
Fold Change: -0.0753
Cell Significance Index: -3.9100 - Cell Name: odontoblast (CL0000060)
Fold Change: -0.0774
Cell Significance Index: -9.9200 - Cell Name: transit amplifying cell of small intestine (CL0009012)
Fold Change: -0.0844
Cell Significance Index: -1.7500 - Cell Name: GABAergic amacrine cell (CL4030027)
Fold Change: -0.0891
Cell Significance Index: -1.1100 - Cell Name: pigmented ciliary epithelial cell (CL0002303)
Fold Change: -0.1258
Cell Significance Index: -18.2800 - Cell Name: dopaminergic neuron (CL0000700)
Fold Change: -0.1286
Cell Significance Index: -36.9900 - Cell Name: hippocampal pyramidal neuron (CL1001571)
Fold Change: -0.1460
Cell Significance Index: -4.1700 - Cell Name: eye photoreceptor cell (CL0000287)
Fold Change: -0.1649
Cell Significance Index: -10.3900 - Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
Fold Change: -0.1759
Cell Significance Index: -18.3200 - Cell Name: tonsil germinal center B cell (CL2000006)
Fold Change: -0.1811
Cell Significance Index: -21.3600 - Cell Name: sebum secreting cell (CL0000317)
Fold Change: -0.1889
Cell Significance Index: -13.3600 - Cell Name: pancreatic D cell (CL0000173)
Fold Change: -0.2142
Cell Significance Index: -45.1200 - Cell Name: lactocyte (CL0002325)
Fold Change: -0.2187
Cell Significance Index: -28.2500 - Cell Name: abnormal cell (CL0001061)
Fold Change: -0.2614
Cell Significance Index: -26.7000 - Cell Name: pancreatic ductal cell (CL0002079)
Fold Change: -0.2714
Cell Significance Index: -31.0900 - Cell Name: endothelial cell of placenta (CL0009092)
Fold Change: -0.2863
Cell Significance Index: -1.7300 - Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
Fold Change: -0.2939
Cell Significance Index: -6.2600 - Cell Name: early pro-B cell (CL0002046)
Fold Change: -0.3066
Cell Significance Index: -19.7800 - Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
Fold Change: -0.4206
Cell Significance Index: -31.3500 - Cell Name: basal cell of prostate epithelium (CL0002341)
Fold Change: -0.4335
Cell Significance Index: -11.8000 - Cell Name: intestinal tuft cell (CL0019032)
Fold Change: -0.4396
Cell Significance Index: -26.9500 - Cell Name: Purkinje cell (CL0000121)
Fold Change: -0.4581
Cell Significance Index: -10.0300 - Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
Fold Change: -0.4701
Cell Significance Index: -37.2300 - Cell Name: OFF midget ganglion cell (CL4033047)
Fold Change: -0.4896
Cell Significance Index: -6.1100 - Cell Name: cardiac muscle cell (CL0000746)
Fold Change: -0.5344
Cell Significance Index: -7.8900 - Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
Fold Change: -0.5881
Cell Significance Index: -18.7300 - Cell Name: L6b glutamatergic cortical neuron (CL4023038)
Fold Change: -0.6109
Cell Significance Index: -20.0000 - Cell Name: glycinergic neuron (CL1001509)
Fold Change: -0.6395
Cell Significance Index: -33.5800 - Cell Name: ON midget ganglion cell (CL4033046)
Fold Change: -0.6402
Cell Significance Index: -8.0800 - Cell Name: neutrophil progenitor cell (CL0000834)
Fold Change: -0.6643
Cell Significance Index: -17.7700 - Cell Name: type I muscle cell (CL0002211)
Fold Change: -0.6816
Cell Significance Index: -16.6300 - Cell Name: transit amplifying cell of colon (CL0009011)
Fold Change: -0.7017
Cell Significance Index: -22.4800 - Cell Name: skeletal muscle fibroblast (CL0011027)
Fold Change: -0.7217
Cell Significance Index: -4.8900 - Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
Fold Change: -0.7437
Cell Significance Index: -25.8500 - Cell Name: sst GABAergic cortical interneuron (CL4023017)
Fold Change: -0.7500
Cell Significance Index: -14.8300 - Cell Name: corneal endothelial cell (CL0000132)
Fold Change: -0.7602
Cell Significance Index: -11.5700
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: 1185807910
Symbol: WRN_HUMAN
Name: DNA helicase, RecQ-like type 3
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 8602509
Title: Positional cloning of the Werner's syndrome gene.
PubMed ID: 8602509
PubMed ID: 16723399
Title: Epigenetic inactivation of the premature aging Werner syndrome gene in human cancer.
PubMed ID: 16723399
PubMed ID: 16421571
Title: DNA sequence and analysis of human chromosome 8.
PubMed ID: 16421571
DOI: 10.1038/nature04406
PubMed ID: 9288107
PubMed ID: 9224595
Title: DNA helicase activity in Werner's syndrome gene product synthesized in a baculovirus system.
PubMed ID: 9224595
PubMed ID: 9611231
Title: Characterization of Werner syndrome protein DNA helicase activity: directionality, substrate dependence and stimulation by replication protein A.
PubMed ID: 9611231
PubMed ID: 9618508
Title: Nucleolar localization of the Werner syndrome protein in human cells.
PubMed ID: 9618508
PubMed ID: 10049920
Title: Evolution of the RECQ family of helicases: a Drosophila homolog, Dmblm, is similar to the human Bloom syndrome gene.
PubMed ID: 10049920
PubMed ID: 10212265
Title: Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n.
PubMed ID: 10212265
PubMed ID: 9989816
Title: Two novel regions of interstitial deletion on chromosome 8p in colorectal cancer.
PubMed ID: 9989816
PubMed ID: 11863428
Title: A minimal exonuclease domain of WRN forms a hexamer on DNA and possesses both 3'- 5' exonuclease and 5'-protruding strand endonuclease activities.
PubMed ID: 11863428
DOI: 10.1021/bi0157161
PubMed ID: 11889123
Title: Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation.
PubMed ID: 11889123
PubMed ID: 12704184
Title: The exonucleolytic and endonucleolytic cleavage activities of human exonuclease 1 are stimulated by an interaction with the carboxyl-terminal region of the Werner syndrome protein.
PubMed ID: 12704184
PubMed ID: 17961633
Title: Interaction of human SUV3 RNA/DNA helicase with BLM helicase; loss of the SUV3 gene results in mouse embryonic lethality.
PubMed ID: 17961633
PubMed ID: 17563354
Title: Werner syndrome protein interacts functionally with translesion DNA polymerases.
PubMed ID: 17563354
PubMed ID: 17525332
Title: ATM and ATR substrate analysis reveals extensive protein networks responsive to DNA damage.
PubMed ID: 17525332
PubMed ID: 18596042
Title: The Werner syndrome protein binds replication fork and Holliday junction DNAs as an oligomer.
PubMed ID: 18596042
PubMed ID: 18669648
Title: A quantitative atlas of mitotic phosphorylation.
PubMed ID: 18669648
PubMed ID: 19413330
Title: Lys-N and trypsin cover complementary parts of the phosphoproteome in a refined SCX-based approach.
PubMed ID: 19413330
DOI: 10.1021/ac9004309
PubMed ID: 19652551
Title: WRN helicase promotes repair of DNA double-strand breaks caused by aberrant mismatch repair of chromium-DNA adducts.
PubMed ID: 19652551
DOI: 10.4161/cc.8.17.9410
PubMed ID: 19283071
Title: The Werner syndrome helicase/exonuclease processes mobile D-loops through branch migration and degradation.
PubMed ID: 19283071
PubMed ID: 19690332
Title: Quantitative phosphoproteomic analysis of T cell receptor signaling reveals system-wide modulation of protein-protein interactions.
PubMed ID: 19690332
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 21639834
Title: Promyelocytic leukemia protein interacts with werner syndrome helicase and regulates double-strand break repair in gamma-irradiation-induced DNA damage responses.
PubMed ID: 21639834
PubMed ID: 21406692
Title: System-wide temporal characterization of the proteome and phosphoproteome of human embryonic stem cell differentiation.
PubMed ID: 21406692
PubMed ID: 22814378
Title: N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.
PubMed ID: 22814378
PubMed ID: 24308539
Title: Systematic genomic identification of colorectal cancer genes delineating advanced from early clinical stage and metastasis.
PubMed ID: 24308539
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 27063109
Title: The Ku-binding motif is a conserved module for recruitment and stimulation of non-homologous end-joining proteins.
PubMed ID: 27063109
DOI: 10.1038/ncomms11242
PubMed ID: 28112733
Title: Site-specific mapping of the human SUMO proteome reveals co-modification with phosphorylation.
PubMed ID: 28112733
DOI: 10.1038/nsmb.3366
PubMed ID: 16339893
Title: Solution structure of a multifunctional DNA- and protein-binding motif of human Werner syndrome protein.
PubMed ID: 16339893
PubMed ID: 16622405
Title: WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing.
PubMed ID: 16622405
DOI: 10.1038/nsmb1088
PubMed ID: 10220139
Title: WRN mutations in Werner syndrome.
PubMed ID: 10220139
DOI: 10.1002/(sici)1098-1004(1999)13:4<271::aid-humu2>3.0.co;2-q
PubMed ID: 17148451
Title: Crystal structure of the HRDC domain of human Werner syndrome protein, WRN.
PubMed ID: 17148451
PubMed ID: 20159463
Title: Structural basis for DNA strand separation by the unconventional winged-helix domain of RecQ helicase WRN.
PubMed ID: 20159463
PubMed ID: 31733588
Title: Ligand binding characteristics of the Ku80 von Willebrand domain.
PubMed ID: 31733588
PubMed ID: 33199508
Title: Structure of the helicase core of Werner helicase, a key target in microsatellite instability cancers.
PubMed ID: 33199508
PubMed ID: 9021029
Title: Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population.
PubMed ID: 9021029
DOI: 10.1002/(sici)1096-8628(19970211)68:4<494::aid-ajmg30>3.0.co;2-l
PubMed ID: 9450180
Title: Werner syndrome: characterization of mutations in the WRN gene in an affected family.
PubMed ID: 9450180
PubMed ID: 23180761
Title: RECQL5 plays co-operative and complementary roles with WRN syndrome helicase.
PubMed ID: 23180761
DOI: 10.1093/nar/gks1134
PubMed ID: 10206685
Title: The 1396del A mutation and a missense mutation or a rare polymorphism of the WRN gene detected in a French Werner family with a severe phenotype and a case of an unusual vulvar cancer.
PubMed ID: 10206685
DOI: 10.1002/(sici)1098-1004(1998)11:5<413::aid-humu16>3.0.co;2-i
PubMed ID: 10069711
Title: Polymorphisms at the Werner locus: I. Newly identified polymorphisms, ethnic variability of 1367Cys/Arg, and its stability in a population of Finnish centenarians.
PubMed ID: 10069711
DOI: 10.1002/(sici)1096-8628(19990219)82:5<399::aid-ajmg8>3.3.co;2-i
PubMed ID: 11161804
Title: The Werner syndrome gene and global sequence variation.
PubMed ID: 11161804
PubMed ID: 16673358
Title: The spectrum of WRN mutations in Werner syndrome patients.
PubMed ID: 16673358
DOI: 10.1002/humu.20337
PubMed ID: 16959974
Title: The consensus coding sequences of human breast and colorectal cancers.
PubMed ID: 16959974
PubMed ID: 18987736
Title: DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome.
PubMed ID: 18987736
DOI: 10.1038/nature07485
Sequence Information:
- Length: 1432
- Mass: 162461
- Checksum: 63F10D19E90AA461
- Sequence:
MSEKKLETTA QQRKCPEWMN VQNKRCAVEE RKACVRKSVF EDDLPFLEFT GSIVYSYDAS DCSFLSEDIS MSLSDGDVVG FDMEWPPLYN RGKLGKVALI QLCVSESKCY LFHVSSMSVF PQGLKMLLEN KAVKKAGVGI EGDQWKLLRD FDIKLKNFVE LTDVANKKLK CTETWSLNSL VKHLLGKQLL KDKSIRCSNW SKFPLTEDQK LYAATDAYAG FIIYRNLEIL DDTVQRFAIN KEEEILLSDM NKQLTSISEE VMDLAKHLPH AFSKLENPRR VSILLKDISE NLYSLRRMII GSTNIETELR PSNNLNLLSF EDSTTGGVQQ KQIREHEVLI HVEDETWDPT LDHLAKHDGE DVLGNKVERK EDGFEDGVED NKLKENMERA CLMSLDITEH ELQILEQQSQ EEYLSDIAYK STEHLSPNDN ENDTSYVIES DEDLEMEMLK HLSPNDNEND TSYVIESDED LEMEMLKSLE NLNSGTVEPT HSKCLKMERN LGLPTKEEEE DDENEANEGE EDDDKDFLWP APNEEQVTCL KMYFGHSSFK PVQWKVIHSV LEERRDNVAV MATGYGKSLC FQYPPVYVGK IGLVISPLIS LMEDQVLQLK MSNIPACFLG SAQSENVLTD IKLGKYRIVY VTPEYCSGNM GLLQQLEADI GITLIAVDEA HCISEWGHDF RDSFRKLGSL KTALPMVPIV ALTATASSSI REDIVRCLNL RNPQITCTGF DRPNLYLEVR RKTGNILQDL QPFLVKTSSH WEFEGPTIIY CPSRKMTQQV TGELRKLNLS CGTYHAGMSF STRKDIHHRF VRDEIQCVIA TIAFGMGINK ADIRQVIHYG APKDMESYYQ EIGRAGRDGL QSSCHVLWAP ADINLNRHLL TEIRNEKFRL YKLKMMAKME KYLHSSRCRR QIILSHFEDK QVQKASLGIM GTEKCCDNCR SRLDHCYSMD DSEDTSWDFG PQAFKLLSAV DILGEKFGIG LPILFLRGSN SQRLADQYRR HSLFGTGKDQ TESWWKAFSR QLITEGFLVE VSRYNKFMKI CALTKKGRNW LHKANTESQS LILQANEELC PKKLLLPSSK TVSSGTKEHC YNQVPVELST EKKSNLEKLY SYKPCDKISS GSNISKKSIM VQSPEKAYSS SQPVISAQEQ ETQIVLYGKL VEARQKHANK MDVPPAILAT NKILVDMAKM RPTTVENVKR IDGVSEGKAA MLAPLLEVIK HFCQTNSVQT DLFSSTKPQE EQKTSLVAKN KICTLSQSMA ITYSLFQEKK MPLKSIAESR ILPLMTIGMH LSQAVKAGCP LDLERAGLTP EVQKIIADVI RNPPVNSDMS KISLIRMLVP ENIDTYLIHM AIEILKHGPD SGLQPSCDVN KRRCFPGSEE ICSSSKRSKE EVGINTETSS AERKRRLPVW FAKGSDTSKK LMDKTKRGGL FS
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.