Details for: FBN2

Gene ID: 2201

Symbol: FBN2

Ensembl ID: ENSG00000138829

Description: fibrillin 2

Associated with

Cells (max top 100)

(Marker Score score is uniquely calculated using our advanced thresholding algorithms to reveal cell-specific gene markers)

  • Cell Name: mesangial cell (CL0000650)
    Fold Change: 15.77
    Marker Score: 19035
  • Cell Name: syncytiotrophoblast cell (CL0000525)
    Fold Change: 12.3
    Marker Score: 10100
  • Cell Name: OFF-bipolar cell (CL0000750)
    Fold Change: 4.47
    Marker Score: 13252
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: 4.05
    Marker Score: 71942
  • Cell Name: epithelial cell of lower respiratory tract (CL0002632)
    Fold Change: 4.02
    Marker Score: 16773
  • Cell Name: retinal bipolar neuron (CL0000748)
    Fold Change: 3.58
    Marker Score: 30255
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: 3.46
    Marker Score: 7592
  • Cell Name: retinal rod cell (CL0000604)
    Fold Change: 2.68
    Marker Score: 7658.5
  • Cell Name: regular ventricular cardiac myocyte (CL0002131)
    Fold Change: 2.49
    Marker Score: 55632
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: 2.19
    Marker Score: 8616
  • Cell Name: retinal cone cell (CL0000573)
    Fold Change: 2.18
    Marker Score: 6254
  • Cell Name: epithelial cell of alveolus of lung (CL0010003)
    Fold Change: 1.61
    Marker Score: 723
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: 1.52
    Marker Score: 20177
  • Cell Name: enteric smooth muscle cell (CL0002504)
    Fold Change: 1.49
    Marker Score: 3504
  • Cell Name: mural cell (CL0008034)
    Fold Change: 1.47
    Marker Score: 168878
  • Cell Name: cardiac endothelial cell (CL0010008)
    Fold Change: 1.47
    Marker Score: 2777
  • Cell Name: immature innate lymphoid cell (CL0001082)
    Fold Change: 1.46
    Marker Score: 2967
  • Cell Name: mesodermal cell (CL0000222)
    Fold Change: 1.43
    Marker Score: 18800
  • Cell Name: respiratory epithelial cell (CL0002368)
    Fold Change: 1.31
    Marker Score: 723
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 1.29
    Marker Score: 20110
  • Cell Name: trophoblast giant cell (CL0002488)
    Fold Change: 1.2
    Marker Score: 387
  • Cell Name: lymphoid lineage restricted progenitor cell (CL0000838)
    Fold Change: 1.19
    Marker Score: 714
  • Cell Name: neuronal brush cell (CL0000555)
    Fold Change: 1.13
    Marker Score: 3784
  • Cell Name: CNS interneuron (CL0000402)
    Fold Change: 1.1
    Marker Score: 529
  • Cell Name: sst GABAergic cortical interneuron (CL4023017)
    Fold Change: 1.08
    Marker Score: 21423
  • Cell Name: cerebellar granule cell precursor (CL0002362)
    Fold Change: 1.04
    Marker Score: 581
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 1.03
    Marker Score: 1241
  • Cell Name: interstitial cell of Cajal (CL0002088)
    Fold Change: 1
    Marker Score: 347
  • Cell Name: cerebral cortex GABAergic interneuron (CL0010011)
    Fold Change: 1
    Marker Score: 71802
  • Cell Name: forebrain radial glial cell (CL0013000)
    Fold Change: 1
    Marker Score: 48027
  • Cell Name: caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.99
    Marker Score: 3821
  • Cell Name: absorptive cell (CL0000212)
    Fold Change: 0.98
    Marker Score: 30407
  • Cell Name: fibroblast of cardiac tissue (CL0002548)
    Fold Change: 0.98
    Marker Score: 5872
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.95
    Marker Score: 2413
  • Cell Name: keratinocyte (CL0000312)
    Fold Change: 0.94
    Marker Score: 786.5
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: 0.94
    Marker Score: 9711
  • Cell Name: mesenchymal stem cell (CL0000134)
    Fold Change: 0.94
    Marker Score: 1442
  • Cell Name: transit amplifying cell (CL0009010)
    Fold Change: 0.93
    Marker Score: 5316
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: 0.91
    Marker Score: 2739
  • Cell Name: renal beta-intercalated cell (CL0002201)
    Fold Change: 0.91
    Marker Score: 289
  • Cell Name: pulmonary interstitial fibroblast (CL0002241)
    Fold Change: 0.9
    Marker Score: 724
  • Cell Name: smooth muscle cell of large intestine (CL1000279)
    Fold Change: 0.9
    Marker Score: 340
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.87
    Marker Score: 5280
  • Cell Name: regular atrial cardiac myocyte (CL0002129)
    Fold Change: 0.87
    Marker Score: 3094.5
  • Cell Name: preosteoblast (CL0007010)
    Fold Change: 0.85
    Marker Score: 241
  • Cell Name: Leydig cell (CL0000178)
    Fold Change: 0.84
    Marker Score: 910
  • Cell Name: kidney proximal straight tubule epithelial cell (CL1000839)
    Fold Change: 0.82
    Marker Score: 1924
  • Cell Name: interstitial cell of ovary (CL0002094)
    Fold Change: 0.81
    Marker Score: 5300
  • Cell Name: early T lineage precursor (CL0002425)
    Fold Change: 0.8
    Marker Score: 611
  • Cell Name: germ cell (CL0000586)
    Fold Change: 0.78
    Marker Score: 1371
  • Cell Name: intestinal epithelial cell (CL0002563)
    Fold Change: 0.77
    Marker Score: 1255
  • Cell Name: brush cell (CL0002204)
    Fold Change: 0.77
    Marker Score: 703
  • Cell Name: endocardial cell (CL0002350)
    Fold Change: 0.76
    Marker Score: 431
  • Cell Name: Cajal-Retzius cell (CL0000695)
    Fold Change: 0.76
    Marker Score: 392
  • Cell Name: mononuclear cell (CL0000842)
    Fold Change: 0.75
    Marker Score: 241
  • Cell Name: mesothelial cell of epicardium (CL0011019)
    Fold Change: 0.69
    Marker Score: 222
  • Cell Name: neutrophil progenitor cell (CL0000834)
    Fold Change: 0.69
    Marker Score: 177
  • Cell Name: interneuron (CL0000099)
    Fold Change: 0.68
    Marker Score: 312
  • Cell Name: taste receptor cell (CL0000209)
    Fold Change: 0.68
    Marker Score: 588
  • Cell Name: smooth muscle myoblast (CL0000514)
    Fold Change: 0.67
    Marker Score: 322
  • Cell Name: fetal cardiomyocyte (CL0002495)
    Fold Change: 0.66
    Marker Score: 218
  • Cell Name: kidney epithelial cell (CL0002518)
    Fold Change: 0.64
    Marker Score: 674
  • Cell Name: meningeal macrophage (CL0000879)
    Fold Change: 0.59
    Marker Score: 165
  • Cell Name: CD14-positive monocyte (CL0001054)
    Fold Change: 0.58
    Marker Score: 1447
  • Cell Name: brainstem motor neuron (CL2000047)
    Fold Change: 0.58
    Marker Score: 337
  • Cell Name: intestinal enteroendocrine cell (CL1001516)
    Fold Change: 0.56
    Marker Score: 444
  • Cell Name: promonocyte (CL0000559)
    Fold Change: 0.55
    Marker Score: 357
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.55
    Marker Score: 324
  • Cell Name: mature NK T cell (CL0000814)
    Fold Change: 0.55
    Marker Score: 256
  • Cell Name: smooth muscle cell of prostate (CL1000487)
    Fold Change: 0.54
    Marker Score: 137
  • Cell Name: neural crest cell (CL0011012)
    Fold Change: 0.54
    Marker Score: 573
  • Cell Name: kidney loop of Henle thin descending limb epithelial cell (CL1001111)
    Fold Change: 0.53
    Marker Score: 576
  • Cell Name: cardiac mesenchymal cell (CL0000569)
    Fold Change: 0.52
    Marker Score: 128
  • Cell Name: microglial cell (CL0000129)
    Fold Change: 0.52
    Marker Score: 941
  • Cell Name: parietal epithelial cell (CL1000452)
    Fold Change: 0.51
    Marker Score: 184
  • Cell Name: kidney capillary endothelial cell (CL1000892)
    Fold Change: 0.49
    Marker Score: 153
  • Cell Name: migratory enteric neural crest cell (CL0002607)
    Fold Change: 0.49
    Marker Score: 457
  • Cell Name: megakaryocyte-erythroid progenitor cell (CL0000050)
    Fold Change: 0.48
    Marker Score: 201
  • Cell Name: stellate neuron (CL0000122)
    Fold Change: 0.48
    Marker Score: 2579
  • Cell Name: epithelial cell of nephron (CL1000449)
    Fold Change: 0.47
    Marker Score: 981
  • Cell Name: kidney interstitial cell (CL1000500)
    Fold Change: 0.47
    Marker Score: 334
  • Cell Name: mesenchymal lymphangioblast (CL0005021)
    Fold Change: 0.47
    Marker Score: 104
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: 0.46
    Marker Score: 789
  • Cell Name: ovarian surface epithelial cell (CL2000064)
    Fold Change: 0.46
    Marker Score: 1263
  • Cell Name: Hofbauer cell (CL3000001)
    Fold Change: 0.46
    Marker Score: 252
  • Cell Name: connective tissue cell (CL0002320)
    Fold Change: 0.44
    Marker Score: 114.5
  • Cell Name: inhibitory interneuron (CL0000498)
    Fold Change: 0.44
    Marker Score: 2035
  • Cell Name: melanocyte (CL0000148)
    Fold Change: 0.43
    Marker Score: 175
  • Cell Name: neuronal receptor cell (CL0000006)
    Fold Change: 0.42
    Marker Score: 188
  • Cell Name: myeloid lineage restricted progenitor cell (CL0000839)
    Fold Change: 0.42
    Marker Score: 146
  • Cell Name: neural cell (CL0002319)
    Fold Change: 0.42
    Marker Score: 202
  • Cell Name: Schwann cell (CL0002573)
    Fold Change: 0.42
    Marker Score: 145
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.42
    Marker Score: 14386
  • Cell Name: lung neuroendocrine cell (CL1000223)
    Fold Change: 0.41
    Marker Score: 115
  • Cell Name: oogonial cell (CL0000024)
    Fold Change: 0.41
    Marker Score: 585
  • Cell Name: glial cell (CL0000125)
    Fold Change: 0.39
    Marker Score: 429
  • Cell Name: skin fibroblast (CL0002620)
    Fold Change: 0.39
    Marker Score: 101
  • Cell Name: granulocyte monocyte progenitor cell (CL0000557)
    Fold Change: 0.39
    Marker Score: 247
  • Cell Name: osteoblast (CL0000062)
    Fold Change: 0.39
    Marker Score: 207
  • Cell Name: chondrocyte (CL0000138)
    Fold Change: 0.36
    Marker Score: 164

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Other Information

## Summary FBN2 is a transmembrane protein that plays a crucial role in the development and maintenance of the extracellular matrix (ECM) in various tissues. It is primarily expressed in cells of the connective tissue and epithelial lining of various organs, including the skin, cartilage, bone, and blood vessels. ## Key characteristics * FBN2 is a large protein with a molecular weight of approximately 130 kDa. * It is a transmembrane protein that is expressed in both endothelial cells and cells of the connective tissue. * It is a key component of the ECM and is involved in the structural integrity and elasticity of tissues. ## Pathways and functions * FBN2 is involved in the formation and maintenance of the ECM in various tissues. * It is a key regulator of bone trabecula formation, as it is expressed in cells of the bone marrow and osteoblasts. * It is also involved in the development of the camera-type eye, where it is expressed in the cells of the iris and lens. * In the embryonic eye, FBN2 is essential for the formation of the lens and the development of the optic nerve. * It is also involved in the degradation of the extracellular matrix and the formation of elastic fibers. * FBN2 is also involved in embryonic eye morphogenesis, embryonic limb morphogenesis, and the development of the cardiovascular system. ## Clinical significance Mutations in the FBN2 gene have been linked to a number of human diseases, including Marfan syndrome, osteoporosis, and retinal dystrophy. These diseases are characterized by abnormal remodeling and degeneration of the ECM, which can lead to tissue weakness and dysfunction. FBN2 is a promising target for the treatment of these diseases. By targeting FBN2, it may be possible to inhibit the abnormal remodeling of the ECM and prevent the development of these diseases.

Genular Protein ID: 1535692116

Symbol: FBN2_HUMAN

Name: N/A

UniProtKB Accession Codes:

P35556 B4DU01 Q59ES6

Database IDs:

AGR 1 Antibodypedia 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 1 CDD 2 CTD 1 ChiTaRS 1 DMDM 1 DNASU 1 DisGeNET 1 DrugBank 3 EMBL 7 EPD 1 Ensembl 1 ExpressionAtlas 1 GO 16 Gene3D 2 GeneCards 1 GeneReviews 1 GeneTree 1 Genevisible 1 GenomeRNAi 1 GlyConnect 1 GlyCosmos 1 GlyGen 1 HGNC 2 HOGENOM 1 HPA 1 InParanoid 1 IntAct 1 InterPro 12 KEGG 1 MANE-Select 1 MIM 5 MINT 1 MalaCards 1 MassIVE 1 MaxQB 1 NCBI Taxonomy 1 OMA 1 OpenTargets 1 Orphanet 2 OrthoDB 1 PANTHER 2 PIR 1 PIRSF 1 PRINTS 1 PRO 1 PROSITE 6 PROSITE-ProRule 1 PathwayCommons 1 PaxDb 1 PeptideAtlas 1 Pfam 8 PharmGKB 1 Pharos 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 2 Pumba 1 RNAct 1 Reactome 3 RefSeq 1 SAM 1 SMART 2 SMR 1 STRING 1 SUPFAM 3 SignaLink 1 SwissPalm 1 TreeFam 1 UCSC 1 UniProtKB 1 VEuPathDB 1 eggNOG 1 iPTMnet 1 jPOST 1 neXtProt 1

Citations:

PubMed ID: 8120105

Title: Structure and expression of fibrillin-2, a novel microfibrillar component preferentially located in elastic matrices.

PubMed ID: 8120105

DOI: 10.1083/jcb.124.5.855

PubMed ID: 14702039

Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15372022

Title: The DNA sequence and comparative analysis of human chromosome 5.

PubMed ID: 15372022

DOI: 10.1038/nature02919

PubMed ID: 1852206

Title: Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes.

PubMed ID: 1852206

DOI: 10.1038/352330a0

PubMed ID: 15131124

Title: MAGP-2 has multiple binding regions on fibrillins and has covalent periodic association with fibrillin-containing microfibrils.

PubMed ID: 15131124

DOI: 10.1074/jbc.m313672200

PubMed ID: 18339631

Title: Targeting of bone morphogenetic protein growth factor complexes to fibrillin.

PubMed ID: 18339631

DOI: 10.1074/jbc.m707820200

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: 23010571

Title: A disintegrin-like and metalloprotease domain containing thrombospondin type 1 motif-like 5 (ADAMTSL5) is a novel fibrillin-1-, fibrillin-2-, and heparin-binding member of the ADAMTS superfamily containing a netrin-like module.

PubMed ID: 23010571

DOI: 10.1016/j.matbio.2012.09.003

PubMed ID: 24899048

Title: Rare and common variants in extracellular matrix gene Fibrillin 2 (FBN2) are associated with macular degeneration.

PubMed ID: 24899048

DOI: 10.1093/hmg/ddu276

PubMed ID: 26601954

Title: Characterization of microfibrillar-associated protein 4 (MFAP4) as a tropoelastin- and fibrillin-binding protein involved in elastic fiber formation.

PubMed ID: 26601954

DOI: 10.1074/jbc.m115.681775

PubMed ID: 32329225

Title: Placensin is a glucogenic hormone secreted by human placenta.

PubMed ID: 32329225

DOI: 10.15252/embr.201949530

PubMed ID: 34411563

Title: POGLUT2 and POGLUT3 O-glucosylate multiple EGF repeats in fibrillin-1, -2, and LTBP1 and promote secretion of fibrillin-1.

PubMed ID: 34411563

DOI: 10.1016/j.jbc.2021.101055

PubMed ID: 7493032

Title: Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly.

PubMed ID: 7493032

DOI: 10.1038/ng1295-456

PubMed ID: 9714438

Title: Clustering of FBN2 mutations in patients with congenital contractural arachnodactyly indicates an important role of the domains encoded by exons 24 through 34 during human development.

PubMed ID: 9714438

DOI: 10.1002/(sici)1096-8628(19980724)78:4<350::aid-ajmg9>3.3.co;2-#

PubMed ID: 9737771

Title: A single mutation that results in an Asp-to-His substitution and partial exon skipping in a family with congenital contractural arachnodactyly.

PubMed ID: 9737771

DOI: 10.1007/s004390050777

PubMed ID: 10797416

Title: Two novel fibrillin-2 mutations in congenital contractural arachnodactyly.

PubMed ID: 10797416

DOI: 10.1002/(sici)1096-8628(20000501)92:1<7::aid-ajmg2>3.3.co;2-#

PubMed ID: 11754102

Title: Ten novel FBN2 mutations in congenital contractural arachnodactyly: delineation of the molecular pathogenesis and clinical phenotype.

PubMed ID: 11754102

DOI: 10.1002/humu.10017

PubMed ID: 19006240

Title: Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature.

PubMed ID: 19006240

DOI: 10.1002/humu.20854

PubMed ID: 20799338

Title: Evidence for a recurrent microdeletion at chromosome 16p11.2 associated with congenital anomalies of the kidney and urinary tract (CAKUT) and Hirschsprung disease.

PubMed ID: 20799338

DOI: 10.1002/ajmg.a.33628

PubMed ID: 21248752

Title: Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinoma.

PubMed ID: 21248752

DOI: 10.1038/nature09639

PubMed ID: 25834781

Title: A novel FBN2 mutation in a Chinese family with congenital contractural arachnodactyly.

PubMed ID: 25834781

DOI: 10.1016/j.fob.2015.02.005

PubMed ID: 27196565

Title: Identification of a Novel Missense FBN2 Mutation in a Chinese Family with Congenital Contractural Arachnodactyly Using Exome Sequencing.

PubMed ID: 27196565

DOI: 10.1371/journal.pone.0155908

Sequence Information:

  • Length: 2912
  • Mass: 314775
  • Checksum: 0F0D78319E9911E6
  • Sequence:
    • MGRRRRLCLQ LYFLWLGCVV LWAQGTAGQP QPPPPKPPRP QPPPQQVRSA TAGSEGGFLA 
PEYREEGAAV ASRVRRRGQQ DVLRGPNVCG SRFHSYCCPG WKTLPGGNQC IVPICRNSCG 
DGFCSRPNMC TCSSGQISST CGSKSIQQCS VRCMNGGTCA DDHCQCQKGY IGTYCGQPVC 
ENGCQNGGRC IGPNRCACVY GFTGPQCERD YRTGPCFTQV NNQMCQGQLT GIVCTKTLCC 
ATIGRAWGHP CEMCPAQPQP CRRGFIPNIR TGACQDVDEC QAIPGICQGG NCINTVGSFE 
CRCPAGHKQS ETTQKCEDID ECSIIPGICE TGECSNTVGS YFCVCPRGYV TSTDGSRCID 
QRTGMCFSGL VNGRCAQELP GRMTKMQCCC EPGRCWGIGT IPEACPVRGS EEYRRLCMDG 
LPMGGIPGSA GSRPGGTGGN GFAPSGNGNG YGPGGTGFIP IPGGNGFSPG VGGAGVGAGG 
QGPIITGLTI LNQTIDICKH HANLCLNGRC IPTVSSYRCE CNMGYKQDAN GDCIDVDECT 
SNPCTNGDCV NTPGSYYCKC HAGFQRTPTK QACIDIDECI QNGVLCKNGR CVNTDGSFQC 
ICNAGFELTT DGKNCVDHDE CTTTNMCLNG MCINEDGSFK CICKPGFVLA PNGRYCTDVD 
ECQTPGICMN GHCINSEGSF RCDCPPGLAV GMDGRVCVDT HMRSTCYGGI KKGVCVRPFP 
GAVTKSECCC ANPDYGFGEP CQPCPAKNSA EFHGLCSSGV GITVDGRDIN ECALDPDICA 
NGICENLRGS YRCNCNSGYE PDASGRNCID IDECLVNRLL CDNGLCRNTP GSYSCTCPPG 
YVFRTETETC EDINECESNP CVNGACRNNL GSFNCECSPG SKLSSTGLIC IDSLKGTCWL 
NIQDSRCEVN INGATLKSEC CATLGAAWGS PCERCELDTA CPRGLARIKG VTCEDVNECE 
VFPGVCPNGR CVNSKGSFHC ECPEGLTLDG TGRVCLDIRM EQCYLKWDED ECIHPVPGKF 
RMDACCCAVG AAWGTECEEC PKPGTKEYET LCPRGAGFAN RGDVLTGRPF YKDINECKAF 
PGMCTYGKCR NTIGSFKCRC NSGFALDMEE RNCTDIDECR ISPDLCGSGI CVNTPGSFEC 
ECFEGYESGF MMMKNCMDID ECERNPLLCR GGTCVNTEGS FQCDCPLGHE LSPSREDCVD 
INECSLSDNL CRNGKCVNMI GTYQCSCNPG YQATPDRQGC TDIDECMIMN GGCDTQCTNS 
EGSYECSCSE GYALMPDGRS CADIDECENN PDICDGGQCT NIPGEYRCLC YDGFMASMDM 
KTCIDVNECD LNSNICMFGE CENTKGSFIC HCQLGYSVKK GTTGCTDVDE CEIGAHNCDM 
HASCLNIPGS FKCSCREGWI GNGIKCIDLD ECSNGTHQCS INAQCVNTPG SYRCACSEGF 
TGDGFTCSDV DECAENINLC ENGQCLNVPG AYRCECEMGF TPASDSRSCQ DIDECSFQNI 
CVFGTCNNLP GMFHCICDDG YELDRTGGNC TDIDECADPI NCVNGLCVNT PGRYECNCPP 
DFQLNPTGVG CVDNRVGNCY LKFGPRGDGS LSCNTEIGVG VSRSSCCCSL GKAWGNPCET 
CPPVNSTEYY TLCPGGEGFR PNPITIILED IDECQELPGL CQGGNCINTF GSFQCECPQG 
YYLSEDTRIC EDIDECFAHP GVCGPGTCYN TLGNYTCICP PEYMQVNGGH NCMDMRKSFC 
YRSYNGTTCE NELPFNVTKR MCCCTYNVGK AWNKPCEPCP TPGTADFKTI CGNIPGFTFD 
IHTGKAVDID ECKEIPGICA NGVCINQIGS FRCECPTGFS YNDLLLVCED IDECSNGDNL 
CQRNADCINS PGSYRCECAA GFKLSPNGAC VDRNECLEIP NVCSHGLCVD LQGSYQCICH 
NGFKASQDQT MCMDVDECER HPCGNGTCKN TVGSYNCLCY PGFELTHNND CLDIDECSSF 
FGQVCRNGRC FNEIGSFKCL CNEGYELTPD GKNCIDTNEC VALPGSCSPG TCQNLEGSFR 
CICPPGYEVK SENCIDINEC DEDPNICLFG SCTNTPGGFQ CLCPPGFVLS DNGRRCFDTR 
QSFCFTNFEN GKCSVPKAFN TTKAKCCCSK MPGEGWGDPC ELCPKDDEVA FQDLCPYGHG 
TVPSLHDTRE DVNECLESPG ICSNGQCINT DGSFRCECPM GYNLDYTGVR CVDTDECSIG 
NPCGNGTCTN VIGSFECNCN EGFEPGPMMN CEDINECAQN PLLCAFRCMN TFGSYECTCP 
IGYALREDQK MCKDLDECAE GLHDCESRGM MCKNLIGTFM CICPPGMARR PDGEGCVDEN 
ECRTKPGICE NGRCVNIIGS YRCECNEGFQ SSSSGTECLD NRQGLCFAEV LQTICQMASS 
SRNLVTKSEC CCDGGRGWGH QCELCPLPGT AQYKKICPHG PGYTTDGRDI DECKVMPNLC 
TNGQCINTMG SFRCFCKVGY TTDISGTSCI DLDECSQSPK PCNYICKNTE GSYQCSCPRG 
YVLQEDGKTC KDLDECQTKQ HNCQFLCVNT LGGFTCKCPP GFTQHHTACI DNNECGSQPS 
LCGAKGICQN TPGSFSCECQ RGFSLDATGL NCEDVDECDG NHRCQHGCQN ILGGYRCGCP 
QGYIQHYQWN QCVDENECSN PNACGSASCY NTLGSYKCAC PSGFSFDQFS SACHDVNECS 
SSKNPCNYGC SNTEGGYLCG CPPGYYRVGQ GHCVSGMGFN KGQYLSLDTE VDEENALSPE 
ACYECKINGY SKKDSRQKRS IHEPDPTAVE QISLESVDMD SPVNMKFNLS HLGSKEHILE 
LRPAIQPLNN HIRYVISQGN DDSVFRIHQR NGLSYLHTAK KKLMPGTYTL EITSIPLYKK 
KELKKLEESN EDDYLLGELG EALRMRLQIQ LY

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. For the full schema, download it here.