Details for: MYO15A

Gene ID: 51168

Symbol: MYO15A

Ensembl ID: ENSG00000091536

Description: myosin XVA

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: 32.2736
    Cell Significance Index: -5.0200
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 19.3579
    Cell Significance Index: -4.9100
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 9.7229
    Cell Significance Index: -3.9500
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 4.0796
    Cell Significance Index: -5.0300
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 1.2772
    Cell Significance Index: -5.0400
  • Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
    Fold Change: 0.9692
    Cell Significance Index: 13.8800
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: 0.8540
    Cell Significance Index: 52.3600
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: 0.5025
    Cell Significance Index: 16.1000
  • Cell Name: epithelial cell of nephron (CL1000449)
    Fold Change: 0.4177
    Cell Significance Index: 3.5500
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.3531
    Cell Significance Index: 70.8400
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: 0.2838
    Cell Significance Index: 14.9000
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.2789
    Cell Significance Index: 12.6400
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.2660
    Cell Significance Index: 50.6200
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: 0.2221
    Cell Significance Index: 2.7600
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.2044
    Cell Significance Index: 5.8900
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: 0.2016
    Cell Significance Index: 2.7500
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: 0.1781
    Cell Significance Index: 3.9000
  • Cell Name: skeletal muscle fibroblast (CL0011027)
    Fold Change: 0.1653
    Cell Significance Index: 1.1200
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.1458
    Cell Significance Index: 14.4200
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.1395
    Cell Significance Index: 27.6800
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.1340
    Cell Significance Index: 120.9500
  • Cell Name: keratocyte (CL0002363)
    Fold Change: 0.0914
    Cell Significance Index: 1.4500
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: 0.0844
    Cell Significance Index: 12.2700
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.0760
    Cell Significance Index: 27.2700
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: 0.0753
    Cell Significance Index: 1.4700
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.0729
    Cell Significance Index: 11.8600
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.0704
    Cell Significance Index: 7.6600
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: 0.0676
    Cell Significance Index: 2.3800
  • Cell Name: fibroblast of cardiac tissue (CL0002548)
    Fold Change: 0.0613
    Cell Significance Index: 0.8800
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.0575
    Cell Significance Index: 3.4500
  • Cell Name: retinal ganglion cell (CL0000740)
    Fold Change: 0.0545
    Cell Significance Index: 0.4500
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.0516
    Cell Significance Index: 9.3100
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: 0.0500
    Cell Significance Index: 1.3400
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0493
    Cell Significance Index: 92.8200
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: 0.0390
    Cell Significance Index: 0.8300
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0334
    Cell Significance Index: 51.4400
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: 0.0281
    Cell Significance Index: 3.2800
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.0257
    Cell Significance Index: 47.4000
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 0.0233
    Cell Significance Index: 2.9900
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: 0.0210
    Cell Significance Index: 0.3600
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.0208
    Cell Significance Index: 0.9200
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.0185
    Cell Significance Index: 1.2800
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: 0.0098
    Cell Significance Index: 6.2400
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.0097
    Cell Significance Index: 1.1900
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0085
    Cell Significance Index: 11.5300
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: 0.0076
    Cell Significance Index: 0.2700
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.0069
    Cell Significance Index: 3.7700
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.0054
    Cell Significance Index: 2.3700
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: 0.0037
    Cell Significance Index: 0.1400
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 0.0008
    Cell Significance Index: 0.0200
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.0014
    Cell Significance Index: -0.0300
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -0.0025
    Cell Significance Index: -0.1300
  • Cell Name: OFF midget ganglion cell (CL4033047)
    Fold Change: -0.0032
    Cell Significance Index: -0.0400
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0034
    Cell Significance Index: -1.5600
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0035
    Cell Significance Index: -2.6100
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0052
    Cell Significance Index: -3.9700
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0054
    Cell Significance Index: -3.9700
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0065
    Cell Significance Index: -3.6600
  • Cell Name: CD14-positive, CD16-negative classical monocyte (CL0002057)
    Fold Change: -0.0092
    Cell Significance Index: -0.1700
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: -0.0092
    Cell Significance Index: -1.2700
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.0107
    Cell Significance Index: -0.6000
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.0122
    Cell Significance Index: -3.5100
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0131
    Cell Significance Index: -2.2500
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.0132
    Cell Significance Index: -0.8100
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.0148
    Cell Significance Index: -1.7000
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: -0.0161
    Cell Significance Index: -1.1400
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.0224
    Cell Significance Index: -4.7200
  • Cell Name: mature alpha-beta T cell (CL0000791)
    Fold Change: -0.0275
    Cell Significance Index: -0.1500
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.0283
    Cell Significance Index: -1.3200
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: -0.0284
    Cell Significance Index: -1.9100
  • Cell Name: BEST4+ enteroycte (CL4030026)
    Fold Change: -0.0285
    Cell Significance Index: -0.4300
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.0291
    Cell Significance Index: -3.7600
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.0305
    Cell Significance Index: -3.1200
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: -0.0347
    Cell Significance Index: -0.9500
  • Cell Name: ON midget ganglion cell (CL4033046)
    Fold Change: -0.0357
    Cell Significance Index: -0.4500
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.0358
    Cell Significance Index: -1.1400
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: -0.0363
    Cell Significance Index: -2.2900
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.0368
    Cell Significance Index: -4.3400
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.0413
    Cell Significance Index: -4.3000
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.0462
    Cell Significance Index: -3.4400
  • Cell Name: transit amplifying cell of small intestine (CL0009012)
    Fold Change: -0.0463
    Cell Significance Index: -0.9600
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: -0.0471
    Cell Significance Index: -3.6200
  • Cell Name: centrilobular region hepatocyte (CL0019029)
    Fold Change: -0.0493
    Cell Significance Index: -0.8300
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: -0.0512
    Cell Significance Index: -1.4300
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.0544
    Cell Significance Index: -4.3100
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.0555
    Cell Significance Index: -3.5800
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.0555
    Cell Significance Index: -2.6100
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.0568
    Cell Significance Index: -1.6200
  • Cell Name: hepatoblast (CL0005026)
    Fold Change: -0.0583
    Cell Significance Index: -0.9800
  • Cell Name: sst GABAergic cortical interneuron (CL4023017)
    Fold Change: -0.0617
    Cell Significance Index: -1.2200
  • Cell Name: midget ganglion cell of retina (CL4023188)
    Fold Change: -0.0624
    Cell Significance Index: -0.6500
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.0654
    Cell Significance Index: -2.1400
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -0.0675
    Cell Significance Index: -1.1300
  • Cell Name: near-projecting glutamatergic cortical neuron (CL4023012)
    Fold Change: -0.0678
    Cell Significance Index: -1.6900
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -0.0722
    Cell Significance Index: -1.4500
  • Cell Name: eukaryotic cell (CL0000255)
    Fold Change: -0.0741
    Cell Significance Index: -3.2200
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.0760
    Cell Significance Index: -3.9600
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.0768
    Cell Significance Index: -2.6900
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.0829
    Cell Significance Index: -1.7600
  • Cell Name: periportal region hepatocyte (CL0019026)
    Fold Change: -0.0938
    Cell Significance Index: -1.3900

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:** The MYO15A gene is a member of the myosin superfamily, specifically the myosin-X subfamily. It is characterized by its unique structure, which includes an actin-binding domain and a motor domain. The MYO15A protein is a heterodimeric complex composed of myosin-XVA and its regulatory subunit, MYO15B. This protein exhibits high ATPase activity, enabling it to hydrolyze ATP and generate force for actin-based cell movement. **Pathways and Functions:** The MYO15A gene is involved in various cellular pathways, including: 1. **Actin-based cell projection:** MYO15A is required for the formation of actin-based protrusions, such as filopodia and lamellipodia, which are essential for cell migration, adhesion, and sensing the extracellular environment. 2. **Actin cytoskeleton organization:** MYO15A regulates the organization of the actin cytoskeleton, influencing cell shape, motility, and intracellular transport. 3. **Endocytosis and exocytosis:** MYO15A is involved in the regulation of endocytic and exocytic processes, including the internalization and secretion of proteins and lipids. 4. **Sensory perception:** MYO15A is expressed in sensory neurons and plays a crucial role in the processing of sound and other sensory stimuli. **Clinical Significance:** Dysregulation of the MYO15A gene has been implicated in various human diseases, including: 1. **Inner ear disorders:** Mutations in MYO15A have been associated with Usher syndrome, a disorder characterized by hearing loss and vision impairment. 2. **Neurodevelopmental disorders:** MYO15A has been linked to neurodevelopmental disorders, such as autism spectrum disorder and schizophrenia. 3. **Immune system dysregulation:** MYO15A is expressed in hematopoietic cells and plays a role in immune system function, with dysregulation potentially contributing to autoimmune diseases. In conclusion, the MYO15A gene is a critical regulator of cellular processes, including actin-based cell movement, cytoskeleton organization, and sensory perception. Its dysregulation has been implicated in various human diseases, highlighting the importance of this gene in maintaining cellular homeostasis and overall health. Further research is needed to fully elucidate the functions and clinical significance of the MYO15A gene.

Genular Protein ID: 1301953256

Symbol: MYO15_HUMAN

Name: Unconventional myosin-XV

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 9603736

Title: Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3.

PubMed ID: 9603736

DOI: 10.1126/science.280.5368.1447

PubMed ID: 10552926

Title: Characterization of the human and mouse unconventional myosin XV genes responsible for hereditary deafness DFNB3 and shaker 2.

PubMed ID: 10552926

DOI: 10.1006/geno.1999.5976

PubMed ID: 14702039

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

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 16625196

Title: DNA sequence of human chromosome 17 and analysis of rearrangement in the human lineage.

PubMed ID: 16625196

DOI: 10.1038/nature04689

PubMed ID: 19807924

Title: Identification of SH3 domain interaction partners of human FasL (CD178) by phage display screening.

PubMed ID: 19807924

DOI: 10.1186/1471-2172-10-53

PubMed ID: 11735029

Title: Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.

PubMed ID: 11735029

DOI: 10.1007/s004390100604

PubMed ID: 24926664

Title: Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.

PubMed ID: 24926664

DOI: 10.1371/journal.pone.0099797

Sequence Information:

  • Length: 3530
  • Mass: 395293
  • Checksum: DCCFBAD37BEA6309
  • Sequence:
  • MAKEEDEEKK AKKGKKGKKA PEPEKPKRSL KGTSRLFMGF RDRTPKISKK GQFRSASAFF 
    WGLHTGPQKT KRKRKARTVL KSTSKLMTQM RMGKKKRAMK GKKPSFMVIR FPGRRGYGRL 
    RPRARSLSKA STAINWLTKK FLLKKAEESG SEQATVDAWL QRSSSRMGSR KLPFPSGAEI 
    LRPGGRLRRF PRSRSIYASG EPLGFLPFED EAPFHHSGSR KSLYGLEGFQ DLGEYYDYHR 
    DGDDYYDRQS LHRYEEQEPY LAGLGPYSPA WPPYGDHYYG YPPEDPYDYY HPDYYGGPFD 
    PGYTYGYGYD DYEPPYAPPS GYSSPYSYHD GYEGEAHPYG YYLDPYAPYD APYPPYDLPY 
    HTPYDVPYFD PYGVHYTVPY AEGVYGGGDE AIYPPEVPYF YPEESASAFV YPWVPPPIPS 
    PHNPYAHAMD DIAELEEPED AGVERQGTSF RLPSAAFFEQ QGMDKPARSK LSLIRKFRLF 
    PRPQVKLFGK EKLEVPLPPS LDIPLPLGDA DEEEDEEELP PVSAVPYGHP FWGFLTPRQR 
    NLQRALSAFG AHRGLGFGPE FGRPVPRPAT SLARFLKKTL SEKKPIARLR GSQKARAGGP 
    AVREAAYKRF GYKLAGMDPE KPGTPIVLRR AQPRARSSND ARRPPAPQPA PRTLSHWSAL 
    LSPPVPPRPP SSGPPPAPPL SPALSGLPRP ASPYGSLRRH PPPWAAPAHV PPAPQASWWA 
    FVEPPAVSPE VPPDLLAFPG PRPSFRGSRR RGAAFGFPGA SPRASRRRAW SPLASPQPSL 
    RSSPGLGYCS PLAPPSPQLS LRTGPFQPPF LPPARRPRSL QESPAPRRAA GRLGPPGSPL 
    PGSPRPPSPP LGLCHSPRRS SLNLPSRLPH TWRRLSEPPT RAVKPQVRLP FHRPPRAGAW 
    RAPLEHRESP REPEDSETPW TVPPLAPSWD VDMPPTQRPP SPWPGGAGSR RGFSRPPPVP 
    ENPFLQLLGP VPSPTLQPED PAADMTRVFL GRHHEPGPGQ LTKSAGPTPE KPEEEATLGD 
    PQLPAETKPP TPAPPKDVTP PKDITPPKDV LPEQKTLRPS LSYPLAACDQ TRATWPPWHR 
    WGTLPQAAAP LAPIRAPEPL PKGGERRQAA PGRFAVVMPR VQKLSSFQRV GPATLKPQVQ 
    PIQDPKPRAC SLRWSCLWLR ADAYGPWPRV HTHPQSCHLG PGAACLSLRG SWEEVGPPSW 
    RNKMHSIRNL PSMRFREQHG EDGVEDMTQL EDLQETTVLS NLKIRFERNL IYTYIGSILV 
    SVNPYQMFGI YGPEQVQQYN GRALGENPPH LFAVANLAFA KMLDAKQNQC IIISGESGSG 
    KTEATKLILR YLAAMNQKRE VMQQIKILEA TPLLESFGNA KTVRNDNSSR FGKFVEIFLE 
    GGVISGAITS QYLLEKSRIV FQAKNERNYH IFYELLAGLP AQLRQAFSLQ EAETYYYLNQ 
    GGNCEIAGKS DADDFRRLLA AMEVLGFSSE DQDSIFRILA SILHLGNVYF EKYETDAQEV 
    ASVVSAREIQ AVAELLQISP EGLQKAITFK VTETMREKIF TPLTVESAVD ARDAIAKVLY 
    ALLFSWLITR VNALVSPRQD TLSIAILDIY GFEDLSFNSF EQLCINYANE NLQYLFNKIV 
    FQEEQEEYIR EQIDWQEITF ADNQPCINLI SLKPYGILRI LDDQCCFPQA TDHTFLQKCH 
    YHHGANPLYS KPKMPLPEFT IKHYAGKVTY QVHKFLDKNH DQVRQDVLDL FVRSRTRVVA 
    HLFSSHAPQA APQRLGKSSS VTRLYKAHTV AAKFQQSLLD LVEKMERCNP LFMRCLKPNH 
    KKEPGLFEPD VVMAQLRYSG VLETVRIRKE GFPVRLPFQG FIDRYCCLVA LKHDLPANGD 
    MCVSVLSRLC KVMPNMYRVG VSKLFLKEHL YQLLESMREH VLNLAALTLQ RCLRGFFIKR 
    RFRSLRHKII LLQSRARGYL ARQRYQQMRR SLVKFRSLVH AYVSRRRYLK LRAEWRCQVE 
    GALLWEQEEL SKREVVAVGH LEVPAELAGL LQAVAGLGLA QVPQVAPVRT PRLQAEPRVT 
    LPLDINNYPM AKFVQCHFKE PAFGMLTVPL RTPLTQLPAE HHAEAVSIFK LILRFMGDPH 
    LHGARENIFG NYIVQKGLAV PELRDEILAQ LANQVWHNHN AHNAERGWLL LAACLSGFAP 
    SPCFNKYLLK FVSDYGRNGF QAVCQHRLMQ AMGRAQQQGS GAARTLPPTQ LEWTATYEKA 
    SMALDVGCFN GDQFSCPVHS WSTGEEVAGD ILRHRGLADG WRGWTVAMKN GVQWAELAGH 
    DYVLDLVSDL ELLRDFPRQK SYFIVGTEGP AASRGGPKVV FGNSWDSDED MSTRPQPQEH 
    MPKVLDSDGY SSHNQDGTNG ETEAQRGTAT HQESDSLGEP AVPHKGLDCY LDSLFDPVLS 
    YGDADLEKPT AIAYRMKGGG QPGGGSSSGT EDTPRRPPEP KPIPGLDAST LALQQAFIHK 
    QAVLLAREMT LQATALQQQP LSAALRSLPA EKPPAPEAQP TSVGTGPPAK PVLLRATPKP 
    LAPAPLAKAP RLPIKPVAAP VLAQDQASPE TTSPSPELVR YSTLNSEHFP QPTQQIKNIV 
    RQYQQPFRGG RPEALRKDGG KVFMKRPDPH EEALMILKGQ MTHLAAAPGT QVSREAVALV 
    KPVTSAPRPS MAPTSALPSR SLEPPEELTQ TRLHRLINPN FYGYQDAPWK IFLRKEVFYP 
    KDSYSHPVQL DLLFRQILHD TLSEACLRIS EDERLRMKAL FAQNQLDTQK PLVTESVKRA 
    VVSTARDTWE VYFSRIFPAT GSVGTGVQLL AVSHVGIKLL RMVKGGQEAG GQLRVLRAYS 
    FADILFVTMP SQNMLEFNLA SEKVILFSAR AHQVKTLVDD FILELKKDSD YVVAVRNFLP 
    EDPALLAFHK GDIIHLQPLE PPRVGYSAGC VVRRKVVYLE ELRRRGPDFG WRFGTIHGRV 
    GRFPSELVQP AAAPDFLQLP TEPGRGRAAA VAAAVASAAA AQEVGRRREG PPVRARSADH 
    GEDALALPPY TMLEFAQKYF RDPQRRPQDG LRLKSKEPRE SRTLEDMLCF TKTPLQESLI 
    ELSDSSLSKM ATDMFLAVMR FMGDAPLKGQ SDLDVLCNLL KLCGDHEVMR DECYCQVVKQ 
    ITDNTSSKQD SCQRGWRLLY IVTAYHSCSE VLHPHLTRFL QDVSRTPGLP FQGIAKACEQ 
    NLQKTLRFGG RLELPSSIEL RAMLAGRSSK RQLFLLPGGL ERHLKIKTCT VALDVVEEIC 
    AEMALTRPEA FNEYVIFVVT NRGQHVCPLS RRAYILDVAS EMEQVDGGYM LWFRRVLWDQ 
    PLKFENELYV TMHYNQVLPD YLKGLFSSVP ASRPSEQLLQ QVSKLASLQH RAKDHFYLPS 
    VREVQEYIPA QLYRTTAGST WLNLVSQHRQ QTQALSPHQA RAQFLGLLSA LPMFGSSFFF 
    IQSCSNIAVP APCILAINHN GLNFLSTETH ELMVKFPLKE IQSTRTQRPT ANSSYPYVEI 
    ALGDVAAQRT LQLQLEQGLE LCRVVAVHVE NLLSAHEKRL TLPPSEITLL

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.