Details for: GPSM2

Gene ID: 29899

Symbol: GPSM2

Ensembl ID: ENSG00000121957

Description: G protein signaling modulator 2

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: 170.4327
    Cell Significance Index: -26.5100
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 111.9879
    Cell Significance Index: -28.4100
  • Cell Name: smooth muscle fiber of ileum (CL1000278)
    Fold Change: 71.3268
    Cell Significance Index: -33.6800
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 65.0081
    Cell Significance Index: -26.4100
  • Cell Name: ciliated cell of the bronchus (CL0002332)
    Fold Change: 27.9499
    Cell Significance Index: -26.6900
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 26.7244
    Cell Significance Index: -32.9500
  • Cell Name: epidermal Langerhans cell (CL0002457)
    Fold Change: 10.7741
    Cell Significance Index: -23.5800
  • Cell Name: CD8-positive, alpha-beta regulatory T cell (CL0000795)
    Fold Change: 9.0869
    Cell Significance Index: -27.9100
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 8.5224
    Cell Significance Index: -33.6300
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: 1.7546
    Cell Significance Index: 46.8500
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: 1.6070
    Cell Significance Index: 44.9100
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: 1.3967
    Cell Significance Index: 27.2600
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 1.1085
    Cell Significance Index: 1000.8900
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: 1.0377
    Cell Significance Index: 63.7800
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.9764
    Cell Significance Index: 158.8000
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.8682
    Cell Significance Index: 94.4400
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: 0.8431
    Cell Significance Index: 47.3100
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: 0.8156
    Cell Significance Index: 19.5600
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.7889
    Cell Significance Index: 156.5600
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.6540
    Cell Significance Index: 131.2000
  • Cell Name: skeletal muscle fibroblast (CL0011027)
    Fold Change: 0.6479
    Cell Significance Index: 4.3900
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: 0.6156
    Cell Significance Index: 71.7400
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.5005
    Cell Significance Index: 61.5400
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.4766
    Cell Significance Index: 85.9200
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: 0.4405
    Cell Significance Index: 6.0100
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.3909
    Cell Significance Index: 140.2200
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.3465
    Cell Significance Index: 20.8000
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: 0.3330
    Cell Significance Index: 9.6000
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: 0.2760
    Cell Significance Index: 6.9000
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.2705
    Cell Significance Index: 11.9700
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.2561
    Cell Significance Index: 113.2200
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: 0.2509
    Cell Significance Index: 9.5000
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.2495
    Cell Significance Index: 11.3100
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 0.2494
    Cell Significance Index: 19.1400
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 0.1932
    Cell Significance Index: 133.6300
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.1807
    Cell Significance Index: 12.5000
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: 0.1712
    Cell Significance Index: 10.7900
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: 0.1468
    Cell Significance Index: 3.1800
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.1465
    Cell Significance Index: 14.5000
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: 0.1277
    Cell Significance Index: 4.0900
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.1177
    Cell Significance Index: 22.3900
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.1142
    Cell Significance Index: 15.6800
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.1037
    Cell Significance Index: 56.6300
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.0928
    Cell Significance Index: 171.0600
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0883
    Cell Significance Index: 135.8700
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: 0.0820
    Cell Significance Index: 9.6700
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: 0.0687
    Cell Significance Index: 31.1800
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 0.0528
    Cell Significance Index: 3.5500
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0496
    Cell Significance Index: 93.4400
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0378
    Cell Significance Index: 51.4000
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: 0.0210
    Cell Significance Index: 0.3600
  • Cell Name: type I muscle cell (CL0002211)
    Fold Change: 0.0012
    Cell Significance Index: 0.0300
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -0.0027
    Cell Significance Index: -0.1400
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: -0.0145
    Cell Significance Index: -9.2000
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0382
    Cell Significance Index: -28.0400
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0441
    Cell Significance Index: -33.3900
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0465
    Cell Significance Index: -34.4800
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.0498
    Cell Significance Index: -1.0600
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: -0.0559
    Cell Significance Index: -3.9500
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0605
    Cell Significance Index: -34.1300
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0678
    Cell Significance Index: -42.3400
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.0710
    Cell Significance Index: -2.5000
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.0823
    Cell Significance Index: -23.6800
  • Cell Name: neutrophil progenitor cell (CL0000834)
    Fold Change: -0.1107
    Cell Significance Index: -2.9600
  • Cell Name: fibro/adipogenic progenitor cell (CL0009099)
    Fold Change: -0.1145
    Cell Significance Index: -5.7900
  • Cell Name: odontoblast (CL0000060)
    Fold Change: -0.1354
    Cell Significance Index: -17.3600
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.1428
    Cell Significance Index: -9.2100
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.1487
    Cell Significance Index: -21.6100
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.1536
    Cell Significance Index: -15.6900
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.1660
    Cell Significance Index: -21.4500
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.1722
    Cell Significance Index: -29.4100
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.1801
    Cell Significance Index: -37.9400
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -0.1805
    Cell Significance Index: -3.0200
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.2063
    Cell Significance Index: -9.6200
  • Cell Name: cone retinal bipolar cell (CL0000752)
    Fold Change: -0.2244
    Cell Significance Index: -1.7300
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.2659
    Cell Significance Index: -27.6900
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.2666
    Cell Significance Index: -30.5400
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.2842
    Cell Significance Index: -21.1800
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: -0.2844
    Cell Significance Index: -7.6200
  • Cell Name: basal cell of epidermis (CL0002187)
    Fold Change: -0.2871
    Cell Significance Index: -4.3600
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: -0.2967
    Cell Significance Index: -6.2100
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.3188
    Cell Significance Index: -16.7400
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: -0.3525
    Cell Significance Index: -9.6000
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.3613
    Cell Significance Index: -16.9800
  • Cell Name: fibroblast of cardiac tissue (CL0002548)
    Fold Change: -0.3677
    Cell Significance Index: -5.2800
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.3746
    Cell Significance Index: -7.9500
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.3836
    Cell Significance Index: -30.3800
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.4316
    Cell Significance Index: -22.4800
  • Cell Name: pro-T cell (CL0000827)
    Fold Change: -0.4905
    Cell Significance Index: -12.5300
  • Cell Name: skeletal muscle satellite stem cell (CL0008011)
    Fold Change: -0.5254
    Cell Significance Index: -5.4900
  • Cell Name: hippocampal astrocyte (CL0002604)
    Fold Change: -0.5371
    Cell Significance Index: -7.5100
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.5520
    Cell Significance Index: -33.8400
  • Cell Name: astrocyte of the cerebral cortex (CL0002605)
    Fold Change: -0.5564
    Cell Significance Index: -9.6200
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: -0.6063
    Cell Significance Index: -21.0700
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: -0.6184
    Cell Significance Index: -7.6700
  • Cell Name: OFF midget ganglion cell (CL4033047)
    Fold Change: -0.6367
    Cell Significance Index: -7.9400
  • Cell Name: transit amplifying cell of small intestine (CL0009012)
    Fold Change: -0.6368
    Cell Significance Index: -13.2100
  • Cell Name: BEST4+ enteroycte (CL4030026)
    Fold Change: -0.6516
    Cell Significance Index: -9.8200
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: -0.6649
    Cell Significance Index: -19.0600
  • Cell Name: paneth cell of colon (CL0009009)
    Fold Change: -0.6841
    Cell Significance Index: -10.2500

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** GPSM2 is a protein that belongs to the G protein signaling modulator family. It shares sequence homology with other members of this family, including B4DIF1. The protein has been identified as a GDP-dissociation inhibitor (GDI), which means it regulates the interaction between G proteins and their GDP-bound state. GPSM2 is also involved in regulating the localization of proteins to the cell cortex and the maintenance of centrosome location. Its expression is highly specific to certain cell types, suggesting that it plays a crucial role in regulating cellular processes specific to these cells. **Pathways and Functions** GPSM2 is involved in various cellular pathways, including: 1. **G protein-coupled receptor signaling pathway**: GPSM2 regulates the activity of G proteins, which are essential for transmitting signals from GPCRs to downstream effectors. 2. **Cell cortex**: GPSM2 regulates the localization of proteins to the cell cortex, which is essential for maintaining cellular structure and function. 3. **Centrosome**: GPSM2 is involved in maintaining the location of centrosomes, which are essential for organizing microtubules and regulating cell division. 4. **Mitotic spindle organization**: GPSM2 regulates the organization of the mitotic spindle, which is essential for proper cell division. 5. **Signal transduction**: GPSM2 is involved in regulating the activity of G proteins, which are essential for transmitting signals from GPCRs to downstream effectors. **Clinical Significance** Alterations in GPSM2 expression or function may contribute to various diseases, including: 1. **Neurological disorders**: GPSM2 has been implicated in the regulation of neuronal signaling pathways, and alterations in its expression may contribute to neurological disorders such as Alzheimer's disease and Parkinson's disease. 2. **Cardiovascular disorders**: GPSM2 has been implicated in the regulation of vascular smooth muscle cell signaling pathways, and alterations in its expression may contribute to cardiovascular disorders such as hypertension and atherosclerosis. 3. **Respiratory disorders**: GPSM2 has been implicated in the regulation of pulmonary interstitial fibroblast signaling pathways, and alterations in its expression may contribute to respiratory disorders such as pulmonary fibrosis. In conclusion, GPSM2 is a gene that encodes a protein involved in regulating cellular signaling pathways, particularly those related to G protein-coupled receptor signaling. Its expression is highly specific to certain cell types, suggesting that it plays a crucial role in regulating cellular processes specific to these cells. Alterations in GPSM2 expression or function may contribute to various diseases, including neurological, cardiovascular, and respiratory disorders. Further research is needed to fully understand the role of GPSM2 in human disease and to develop therapeutic strategies to target this gene.

Genular Protein ID: 2794416226

Symbol: GPSM2_HUMAN

Name: G-protein-signaling modulator 2

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 8973305

Title: Identification and cDNA cloning of a novel human mosaic protein, LGN, based on interaction with G alpha i2.

PubMed ID: 8973305

DOI: 10.1016/s0378-1119(96)00456-8

PubMed ID: 16710414

Title: The DNA sequence and biological annotation of human chromosome 1.

PubMed ID: 16710414

DOI: 10.1038/nature04727

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: 11781568

Title: A mammalian partner of inscuteable binds NuMA and regulates mitotic spindle organization.

PubMed ID: 11781568

DOI: 10.1038/ncb1201-1069

PubMed ID: 15632202

Title: Direct binding of Lgl2 to LGN during mitosis and its requirement for normal cell division.

PubMed ID: 15632202

DOI: 10.1074/jbc.c400440200

PubMed ID: 16458856

Title: Two forms of human Inscuteable-related protein that links Par3 to the Pins homologues LGN and AGS3.

PubMed ID: 16458856

DOI: 10.1016/j.bbrc.2006.01.050

PubMed ID: 18669648

Title: A quantitative atlas of mitotic phosphorylation.

PubMed ID: 18669648

DOI: 10.1073/pnas.0805139105

PubMed ID: 20602914

Title: Whole exome sequencing and homozygosity mapping identify mutation in the cell polarity protein GPSM2 as the cause of nonsyndromic hearing loss DFNB82.

PubMed ID: 20602914

DOI: 10.1016/j.ajhg.2010.05.010

PubMed ID: 20068231

Title: Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.

PubMed ID: 20068231

DOI: 10.1126/scisignal.2000475

PubMed ID: 21816348

Title: LGN/mInsc and LGN/NuMA complex structures suggest distinct functions in asymmetric cell division for the Par3/mInsc/LGN and Galphai/LGN/NuMA pathways.

PubMed ID: 21816348

DOI: 10.1016/j.molcel.2011.07.011

PubMed ID: 22578326

Title: GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndrome.

PubMed ID: 22578326

DOI: 10.1016/j.ajhg.2012.04.008

PubMed ID: 22327364

Title: Chromosome- and spindle-pole-derived signals generate an intrinsic code for spindle position and orientation.

PubMed ID: 22327364

DOI: 10.1038/ncb2440

PubMed ID: 23186163

Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.

PubMed ID: 23186163

DOI: 10.1021/pr300630k

PubMed ID: 26766442

Title: SAPCD2 controls spindle orientation and asymmetric divisions by negatively regulating the Galphai-LGN-NuMA ternary complex.

PubMed ID: 26766442

DOI: 10.1016/j.devcel.2015.12.016

PubMed ID: 27462074

Title: Nuclear mitotic apparatus (NuMA) interacts with and regulates astrin at the mitotic spindle.

PubMed ID: 27462074

DOI: 10.1074/jbc.m116.724831

PubMed ID: 22074847

Title: Structural basis for interaction between the conserved cell polarity proteins Inscuteable and Leu-Gly-Asn repeat-enriched protein (LGN).

PubMed ID: 22074847

DOI: 10.1073/pnas.1110951108

PubMed ID: 25664792

Title: Structural basis for the recognition of the scaffold protein Frmpd4/Preso1 by the TPR domain of the adaptor protein LGN.

PubMed ID: 25664792

DOI: 10.1107/s2053230x14028143

Sequence Information:

  • Length: 684
  • Mass: 76662
  • Checksum: D007A4765F57CB90
  • Sequence:
  • MEENLISMRE DHSFHVRYRM EASCLELALE GERLCKSGDC RAGVSFFEAA VQVGTEDLKT 
    LSAIYSQLGN AYFYLHDYAK ALEYHHHDLT LARTIGDQLG EAKASGNLGN TLKVLGNFDE 
    AIVCCQRHLD ISRELNDKVG EARALYNLGN VYHAKGKSFG CPGPQDVGEF PEEVRDALQA 
    AVDFYEENLS LVTALGDRAA QGRAFGNLGN THYLLGNFRD AVIAHEQRLL IAKEFGDKAA 
    ERRAYSNLGN AYIFLGEFET ASEYYKKTLL LARQLKDRAV EAQSCYSLGN TYTLLQDYEK 
    AIDYHLKHLA IAQELNDRIG EGRACWSLGN AYTALGNHDQ AMHFAEKHLE ISREVGDKSG 
    ELTARLNLSD LQMVLGLSYS TNNSIMSENT EIDSSLNGVR PKLGRRHSME NMELMKLTPE 
    KVQNWNSEIL AKQKPLIAKP SAKLLFVNRL KGKKYKTNSS TKVLQDASNS IDHRIPNSQR 
    KISADTIGDE GFFDLLSRFQ SNRMDDQRCC LQEKNCHTAS TTTSSTPPKM MLKTSSVPVV 
    SPNTDEFLDL LASSQSRRLD DQRASFSNLP GLRLTQNSQS VLSHLMTNDN KEADEDFFDI 
    LVKCQGSRLD DQRCAPPPAT TKGPTVPDED FFSLILRSQG KRMDEQRVLL QRDQNRDTDF 
    GLKDFLQNNA LLEFKNSGKK SADH

Genular Protein ID: 2535217878

Symbol: B4DIF1_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 683
  • Mass: 76575
  • Checksum: E2600531709DCAE5
  • Sequence:
  • MEENLISMRE DHSFHVRYRM EASCLELALE GERLCKSGDC RAGVSFFEAA VQVGTEDLKT 
    LSAIYSQLGN AYFYLHDYAK ALEYHHHDLT LARTIGDQLG EAKASGNLGN TLKVLGNFDE 
    AIVCCQRHLD ISRELNDKVG EARALYNLGN VYHAKGKSFG CPGPQDVGEF PEEVRDALQA 
    AVDFYEENLS LVTALGDRAA QGRAFGNLGN THYLLGNFRD AVIAHEQRLL IAKEFGDKAA 
    ERRAYSNLGN AYIFLGEFET ASEYYKKTLL LARQLKDRAV EAQSCYSLGN TYTLLQDYEK 
    AIDYHLKHLA IAQELNDRIG EGRACWSLGN AYTALGNHDQ AMHFAEKHLE ISREVGDKSG 
    ELTARLNLSD LQMVLGLSYS TNNSIMSENT EIDSSLNGVR PKLGRRHSME NMELMKLTPE 
    KVQNWNSEIL AKQKPLIAKP SAKLLFVNRL KGKKYKTNSS TKVLQDASNS IDHRIPNSQR 
    KISADTIGDE GFFDLLSRFQ SNRMDDQRCC LQEKNCHTAS TTTSTPPKMM LKTSSVPVVS 
    PNTDEFLDLL ASSQSRRLDD QRASFSNLPG LRLTQNSQSV LSHLMTNDNK EADEDFFDIL 
    VKCQGSRLDD QRCAPPPATT KGPTVPDEDF FSLILRSQGK RMDEQRVLLQ RDQNRDTDFG 
    LKDFLQNNAL LEFKNSGKKS ADH

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.