Details for: TECTA

Gene ID: 7007

Symbol: TECTA

Ensembl ID: ENSG00000109927

Description: tectorin alpha

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: 37.9954
    Cell Significance Index: -5.9100
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 23.3004
    Cell Significance Index: -5.9100
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 12.3075
    Cell Significance Index: -5.0000
  • Cell Name: ciliated cell of the bronchus (CL0002332)
    Fold Change: 5.2684
    Cell Significance Index: -5.0300
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 4.7690
    Cell Significance Index: -5.8800
  • Cell Name: epidermal Langerhans cell (CL0002457)
    Fold Change: 1.0463
    Cell Significance Index: -2.2900
  • Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
    Fold Change: 0.6340
    Cell Significance Index: 9.0800
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: 0.5136
    Cell Significance Index: 19.4500
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: 0.4788
    Cell Significance Index: 15.3400
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.4565
    Cell Significance Index: 20.1900
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: 0.4427
    Cell Significance Index: 27.1400
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: 0.3683
    Cell Significance Index: 8.0700
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.2950
    Cell Significance Index: 59.1700
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.2845
    Cell Significance Index: 54.1400
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: 0.2172
    Cell Significance Index: 5.8200
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.2053
    Cell Significance Index: 73.6500
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 0.1245
    Cell Significance Index: 9.5600
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 0.0660
    Cell Significance Index: 4.4400
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.0646
    Cell Significance Index: 58.3300
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.0616
    Cell Significance Index: 6.1000
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.0560
    Cell Significance Index: 3.3600
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: 0.0550
    Cell Significance Index: 1.5700
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: 0.0521
    Cell Significance Index: 3.2000
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.0422
    Cell Significance Index: 4.6000
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: 0.0332
    Cell Significance Index: 4.8200
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.0310
    Cell Significance Index: 5.0400
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: 0.0274
    Cell Significance Index: 1.5400
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: 0.0234
    Cell Significance Index: 0.5600
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 0.0160
    Cell Significance Index: 0.4000
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.0107
    Cell Significance Index: 2.1300
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: 0.0035
    Cell Significance Index: 0.0600
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0016
    Cell Significance Index: 3.0400
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: -0.0008
    Cell Significance Index: -1.4800
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: -0.0010
    Cell Significance Index: -1.3400
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: -0.0016
    Cell Significance Index: -2.4900
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: -0.0017
    Cell Significance Index: -0.0500
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: -0.0024
    Cell Significance Index: -1.5300
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.0026
    Cell Significance Index: -0.0900
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: -0.0034
    Cell Significance Index: -0.2400
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0056
    Cell Significance Index: -4.1700
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0060
    Cell Significance Index: -2.7200
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0070
    Cell Significance Index: -5.1100
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0075
    Cell Significance Index: -5.6500
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: -0.0082
    Cell Significance Index: -4.4700
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0082
    Cell Significance Index: -5.1200
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0083
    Cell Significance Index: -4.6800
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: -0.0085
    Cell Significance Index: -3.7700
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.0118
    Cell Significance Index: -0.2600
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: -0.0126
    Cell Significance Index: -0.5700
  • Cell Name: L6 corticothalamic-projecting glutamatergic cortical neuron (CL4023042)
    Fold Change: -0.0136
    Cell Significance Index: -0.1500
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: -0.0146
    Cell Significance Index: -2.6400
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.0168
    Cell Significance Index: -4.8200
  • Cell Name: eukaryotic cell (CL0000255)
    Fold Change: -0.0183
    Cell Significance Index: -0.8000
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.0185
    Cell Significance Index: -0.5900
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.0188
    Cell Significance Index: -0.4000
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0228
    Cell Significance Index: -3.8900
  • Cell Name: odontoblast (CL0000060)
    Fold Change: -0.0239
    Cell Significance Index: -3.0700
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.0255
    Cell Significance Index: -5.3700
  • Cell Name: early T lineage precursor (CL0002425)
    Fold Change: -0.0262
    Cell Significance Index: -0.3800
  • Cell Name: sst GABAergic cortical interneuron (CL4023017)
    Fold Change: -0.0263
    Cell Significance Index: -0.5200
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.0291
    Cell Significance Index: -2.9700
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: -0.0301
    Cell Significance Index: -4.1300
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.0337
    Cell Significance Index: -3.8600
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: -0.0366
    Cell Significance Index: -4.5000
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: -0.0398
    Cell Significance Index: -2.5100
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: -0.0420
    Cell Significance Index: -4.8900
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.0420
    Cell Significance Index: -1.0800
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.0430
    Cell Significance Index: -5.5600
  • Cell Name: BEST4+ enteroycte (CL4030026)
    Fold Change: -0.0445
    Cell Significance Index: -0.6700
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.0446
    Cell Significance Index: -2.0800
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.0478
    Cell Significance Index: -5.6400
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.0535
    Cell Significance Index: -1.7500
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.0546
    Cell Significance Index: -5.6800
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -0.0568
    Cell Significance Index: -2.9500
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.0682
    Cell Significance Index: -5.4000
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -0.0732
    Cell Significance Index: -1.4700
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.0735
    Cell Significance Index: -3.8300
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.0742
    Cell Significance Index: -5.5300
  • Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
    Fold Change: -0.0824
    Cell Significance Index: -1.7800
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: -0.0834
    Cell Significance Index: -2.3300
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: -0.0836
    Cell Significance Index: -1.0400
  • Cell Name: near-projecting glutamatergic cortical neuron (CL4023012)
    Fold Change: -0.0838
    Cell Significance Index: -2.0900
  • Cell Name: keratocyte (CL0002363)
    Fold Change: -0.0851
    Cell Significance Index: -1.3500
  • Cell Name: corneal epithelial cell (CL0000575)
    Fold Change: -0.0864
    Cell Significance Index: -1.2300
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.0890
    Cell Significance Index: -5.7500
  • Cell Name: OFF midget ganglion cell (CL4033047)
    Fold Change: -0.0890
    Cell Significance Index: -1.1100
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.0909
    Cell Significance Index: -4.7700
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.0918
    Cell Significance Index: -3.2200
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.0934
    Cell Significance Index: -1.9900
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.0992
    Cell Significance Index: -4.6600
  • Cell Name: regular atrial cardiac myocyte (CL0002129)
    Fold Change: -0.1016
    Cell Significance Index: -1.3700
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: -0.1091
    Cell Significance Index: -2.1300
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: -0.1097
    Cell Significance Index: -1.6200
  • Cell Name: glutamatergic neuron (CL0000679)
    Fold Change: -0.1101
    Cell Significance Index: -1.2000
  • Cell Name: ON midget ganglion cell (CL4033046)
    Fold Change: -0.1133
    Cell Significance Index: -1.4300
  • Cell Name: lens fiber cell (CL0011004)
    Fold Change: -0.1173
    Cell Significance Index: -3.7100
  • Cell Name: L6 intratelencephalic projecting glutamatergic neuron of the primary motor cortex (CL4023050)
    Fold Change: -0.1184
    Cell Significance Index: -1.5800
  • Cell Name: type I muscle cell (CL0002211)
    Fold Change: -0.1324
    Cell Significance Index: -3.2300
  • Cell Name: retinal ganglion cell (CL0000740)
    Fold Change: -0.1363
    Cell Significance Index: -1.1300
  • Cell Name: stratified epithelial cell (CL0000079)
    Fold Change: -0.1400
    Cell Significance Index: -5.1400

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. **Transmembrane Protein**: TECTA is a transmembrane protein, consisting of an extracellular domain, a transmembrane domain, and an intracellular domain. 2. **Cell-Matrix Adhesion**: TECTA mediates cell-matrix adhesion, enabling cells to maintain their position and structure within tissues. 3. **Protein Synthesis Regulation**: TECTA regulates protein synthesis by influencing the metabolism of proteins, particularly GPI-anchored proteins. 4. **Sensory Perception**: TECTA is involved in sensory perception, particularly sound, through its role in auditory receptor cell stereocilium organization. 5. **Widespread Expression**: TECTA is expressed in various cell types, including hematopoietic stem cells, goblet cells, and GABAergic interneurons. **Pathways and Functions:** 1. **Auditory Receptor Cell Stereocilium Organization**: TECTA is essential for the formation and maintenance of auditory receptor cell stereocilia, which are crucial for sound perception. 2. **Cell-Matrix Adhesion**: TECTA mediates cell-matrix adhesion, enabling cells to maintain their position and structure within tissues. 3. **Extracellular Matrix Regulation**: TECTA regulates the structure and composition of the extracellular matrix, influencing cell behavior and tissue homeostasis. 4. **Protein Synthesis and Modulation**: TECTA modulates protein synthesis, particularly GPI-anchored proteins, which are involved in various cellular processes. 5. **Glycosylation and Anchorage**: TECTA is involved in the synthesis of GPI-anchored proteins, which are anchored to the plasma membrane through a glycosylphosphatidylinositol (GPI) anchor. **Clinical Significance:** 1. **Auditory Defects**: Mutations in the TECTA gene have been associated with auditory defects, including hearing loss and vestibular dysfunction. 2. **Gastrointestinal Disorders**: TECTA expression has been linked to gastrointestinal disorders, such as ulcerative colitis and Crohn's disease, where goblet cell dysfunction is a hallmark. 3. **Neurological Disorders**: TECTA expression has been observed in GABAergic interneurons, suggesting its potential role in neurological disorders, such as epilepsy and autism spectrum disorder. 4. **Cancer and Metastasis**: TECTA's role in cell-matrix adhesion and protein synthesis regulation may contribute to cancer progression and metastasis. In conclusion, the TECTA gene is a complex and multifaceted molecule that plays a critical role in maintaining tissue homeostasis, regulating protein synthesis, and modulating sensory perception. Further research is necessary to elucidate the full extent of its clinical significance and potential therapeutic applications.

Genular Protein ID: 1572298959

Symbol: TECTA_HUMAN

Name: Alpha-tectorin

UniProtKB Accession Codes:

O75443

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 1 CDD 1 CTD 1 ChiTaRS 1 DNASU 1 DisGeNET 1 EMBL 25 Ensembl 2 ExpressionAtlas 1 GO 9 Gene3D 3 GeneCards 1 GeneReviews 1 GeneTree 1 GeneWiki 1 GenomeRNAi 1 GlyCosmos 1 GlyGen 1 HGNC 1 HOGENOM 1 HPA 1 InParanoid 1 IntAct 1 InterPro 12 KEGG 1 MANE-Select 1 MIM 5 MINT 1 MalaCards 1 MassIVE 1 NCBI Taxonomy 1 OMA 1 OpenTargets 1 Orphanet 2 OrthoDB 1 PANTHER 2 PRO 1 PROSITE 4 PathwayCommons 1 PaxDb 1 PeptideAtlas 1 Pfam 6 Pharos 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 1 RNAct 1 Reactome 1 RefSeq 1 SMART 6 SMR 1 STRING 1 SUPFAM 1 SignaLink 1 TCDB 1 TreeFam 1 UCSC 1 VEuPathDB 1 eggNOG 2 iPTMnet 1 neXtProt 1

Citations:

PubMed ID: 9590290

Title: Mutations in the human alpha-tectorin gene cause autosomal dominant non-syndromic hearing impairment.

PubMed ID: 9590290

DOI: 10.1038/ng0598-60

PubMed ID: 16554811

Title: Human chromosome 11 DNA sequence and analysis including novel gene identification.

PubMed ID: 16554811

DOI: 10.1038/nature04632

PubMed ID: 21368133

Title: Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).

PubMed ID: 21368133

DOI: 10.1073/pnas.1005842108

PubMed ID: 10196713

Title: Mutation in the zonadhesin-like domain of alpha-tectorin associated with autosomal dominant non-syndromic hearing loss.

PubMed ID: 10196713

DOI: 10.1038/sj.ejhg.5200273

PubMed ID: 10987647

Title: Alpha-tectorin involvement in hearing disabilities: one gene -- two phenotypes.

PubMed ID: 10987647

DOI: 10.1007/s004390051091

PubMed ID: 9949200

Title: An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21.

PubMed ID: 9949200

DOI: 10.1093/hmg/8.3.409

PubMed ID: 11333869

Title: A cysteine substitution in the zona pellucida domain of alpha-tectorin results in autosomal dominant, postlingual, progressive, mid frequency hearing loss in a Spanish family.

PubMed ID: 11333869

DOI: 10.1136/jmg.38.5.e13

PubMed ID: 12162770

Title: Association of clinical features with mutation of TECTA in a family with autosomal dominant hearing loss.

PubMed ID: 12162770

DOI: 10.1001/archotol.128.8.913

PubMed ID: 12746400

Title: Distinctive audiometric profile associated with DFNB21 alleles of TECTA.

PubMed ID: 12746400

DOI: 10.1136/jmg.40.5.360

PubMed ID: 15319541

Title: A genotype-phenotype correlation with gender-effect for hearing impairment caused by TECTA mutations.

PubMed ID: 15319541

DOI: 10.1159/000080347

PubMed ID: 16718611

Title: A novel TECTA mutation in a Dutch DFNA8/12 family confirms genotype-phenotype correlation.

PubMed ID: 16718611

DOI: 10.1007/s10162-006-0033-z

PubMed ID: 16959974

Title: The consensus coding sequences of human breast and colorectal cancers.

PubMed ID: 16959974

DOI: 10.1126/science.1133427

PubMed ID: 17661817

Title: Audioprofiling identifies TECTA and GJB2-related deafness segregating in a single extended pedigree.

PubMed ID: 17661817

DOI: 10.1111/j.1399-0004.2007.00828.x

PubMed ID: 20947814

Title: Two novel missense mutations in the TECTA gene in Korean families with autosomal dominant nonsyndromic hearing loss.

PubMed ID: 20947814

PubMed ID: 21520338

Title: DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.

PubMed ID: 21520338

DOI: 10.1002/humu.21512

Sequence Information:

  • Length: 2155
  • Mass: 239527
  • Checksum: A7CB1CD9E7C594C3
  • Sequence:
    • MNYSSFLRIW VSFIFALVQH QAQPRELMYP FWQNDTKTPK VDDGSSSEIK LAIPVFFFGV 
PYRTVYVNNN GVVSFNVLVS QFTPESFPLT DGRAFVAPFW ADVHNGIRGE IYYRETMEPA 
ILKRATKDIR KYFKDMATFS ATWVFIVTWE EVTFYGGSST TPVNTFQAVL VSDGSYTFTL 
FNYYEINWTT GTASGGDPLT GLGGVMAQAG FNGGNLTNFF SLPGSRTPEI VNIQETTNVN 
VPGRWAFKVD GKEIDPANGC TSRGQFLRRG EVFWDDLNCT VKCRCLDFNN EIYCQEASCS 
PYEVCEPKGK FFYCSAVETS TCVVFGEPHY HTFDGFLFHF QGSCAYLLAR QCLQTSSLPF 
FSVEAKNEHR RGSAVSWVKE LSVEVNGYKI LIPKGSYGRV KVNDLVTSLP VTLDLGTVKI 
YQSGISTAVE TDFGLLVTFD GQHYASISVP GSYINSTCGL CGNYNKNPLD DFLRPDGRPA 
MSVLDLGESW RVYHADWKCD SGCVDNCTQC DAATEALYFG SDYCGFLNKT DGPLWECGTV 
VDPTAFVHSC VYDLCSVRDN GTLLCQAIQA YALVCQALGI PIGDWRTQTG CVSTVQCPSF 
SHYSVCTSSC PDTCSDLTAS RNCATPCTEG CECNQGFVLS TSQCVPLHKC GCDFDGHYYT 
MGEFFWATAN CTVQCLCEEG GDVYCFNKTC GSGEVCAVED GYQGCFPKRE TVCLLSQNQV 
LHTFDGASYA FPSEFSYTLL KTCPERPEYL EIDINKKKPD AGPAWLRGLR ILVADQEVKI 
GGIGASEVKL NGQEVELPFF HPSGKLEIYR NKNSTTVESK GVVTVQYSDI GLLYIRLSTT 
YFNCTGGLCG FYNANASDEF CLPNGKCTDN LAVFLESWTT FEEICNGECG DLLKACNNDS 
ELLKFYRSRS RCGIINDPSN SSFLECHGVV NVTAYYRTCL FRLCQSGGNE SELCDSVARY 
ASACKNADVE VGPWRTYDFC PLECPENSHF EECITCTETC ETLTLGPICV DSCSEGCQCD 
EGYALLGSQC VTRSECGCNF EGHQLATNET FWVDLDCQIF CYCSGTDNRV HCETIPCKDD 
EYCMEEGGLY YCQARTDASC IVSGYGHYLT FDGFPFDFQT SCPLILCTTG SRPSSDSFPK 
FVVTAKNEDR DPSLALWVKQ VDVTVFGYSI VIHRAYKHTV LVNSERLYLP LKLGQGKINI 
FSFGFHVVVE TDFGLKVVYD WKTFLSITVP RSMQNSTYGL CGRYNGNPDD DLEMPMGLLA 
SSVNEFGQSW VKRDTFCQVG CGDRCPSCAK VEGFSKVQQL CSLIPNQNAA FSKCHSKVNP 
TFFYKNCLFD SCIDGGAVQT ACSWLQNYAS TCQTQGITVT GWRNYTSCTV TCPPNSHYES 
CVSVCQPRCA AIRLKSDCSH YCVEGCHCDA GYVLNGKSCI LPHSCGCYSD GKYYEPKQLF 
WNSDCTRRCR CFRRNVIQCD PRQCKSDEEC ALRNGVRGCF STKTSYCLAA GGGVFRTFDG 
AFLRFPANCA FVLSTICQKL PDISFQLIIN FDKWSAPNLT IISPVYFYIN EEQILINDRN 
TVKVNGTQVN VPFITGLATK IYSSEGFLVI DTSPDIQIYY NGFNVIKISI SERLQNKVCG 
LCGNFNGDLT DDYVTLRGKP VVSSVVLAQS WKTNGMQKRP LAPSCNELQF SQYAAMCDNV 
HIQKMQGDGY CLKLTDMKGF FQPCYGLLDP LPFYESCYLD GCYSHKKFQL CGSLAAYGEA 
CRSFGILSTE WIEKENCSGV VEDPCVGADC PNRTCELGNG RELCGCIEPP PYGNNSHDII 
DAEVTCKAAQ MEVSISKCKL FQLGFEREGV RINDRQCTGI EGEDFISFQI NNTKGNCGNI 
VQSNGTHIMY KNTLWIESAN NTGNIITRDR TINVEFSCAY ELDIKISLDS VVKPMLSVIN 
LTVPTQEGSF ITKMALYKNA SYKHPYRQGE VVLTTRDVLY VGVFVVGADA THLILTLNKC 
YATPTRDSND KLRYFIIEGG CQNLKDNTIG IEENAVSLTC RFHVTVFKFI GDYDEVHLHC 
AVSLCDSEKY SCKITCPHNS RIATDYTKEP KEQIISVGPI RRKRLDWCED NGGCEQICTS 
RVDGPLCSCV TGTLQEDGKS CRASNSSMEL QVWTLLLIMI QISLWHFVYK SGTTS

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.