Details for: TPM2

Gene ID: 7169

Symbol: TPM2

Ensembl ID: ENSG00000198467

Description: tropomyosin 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: 287.6977
    Cell Significance Index: -44.7500
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 175.8374
    Cell Significance Index: -44.6000
  • Cell Name: embryonic stem cell (CL0002322)
    Fold Change: 106.9796
    Cell Significance Index: -44.0700
  • Cell Name: smooth muscle fiber of ileum (CL1000278)
    Fold Change: 83.6859
    Cell Significance Index: -39.5100
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 36.3030
    Cell Significance Index: -44.7600
  • Cell Name: enteric smooth muscle cell (CL0002504)
    Fold Change: 23.5859
    Cell Significance Index: 124.1100
  • Cell Name: theca cell (CL0000503)
    Fold Change: 12.7353
    Cell Significance Index: 74.8200
  • Cell Name: perivascular cell (CL4033054)
    Fold Change: 11.9574
    Cell Significance Index: 55.2100
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 11.2847
    Cell Significance Index: -44.5300
  • Cell Name: skeletal muscle myoblast (CL0000515)
    Fold Change: 9.9565
    Cell Significance Index: 108.2400
  • Cell Name: type II muscle cell (CL0002212)
    Fold Change: 9.8400
    Cell Significance Index: 158.7700
  • Cell Name: epidermal Langerhans cell (CL0002457)
    Fold Change: 8.3570
    Cell Significance Index: -18.2900
  • Cell Name: type I muscle cell (CL0002211)
    Fold Change: 7.6072
    Cell Significance Index: 185.6100
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 5.3066
    Cell Significance Index: 728.7500
  • Cell Name: interstitial cell of ovary (CL0002094)
    Fold Change: 5.2992
    Cell Significance Index: 67.8700
  • Cell Name: pulmonary interstitial fibroblast (CL0002241)
    Fold Change: 5.0333
    Cell Significance Index: 31.1400
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: 5.0261
    Cell Significance Index: 105.2100
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: 3.8185
    Cell Significance Index: 109.4600
  • Cell Name: vascular lymphangioblast (CL0005022)
    Fold Change: 2.9909
    Cell Significance Index: 52.8500
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 2.9630
    Cell Significance Index: 379.8400
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: 2.7313
    Cell Significance Index: 73.1900
  • Cell Name: germ cell (CL0000586)
    Fold Change: 2.4852
    Cell Significance Index: 18.7700
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 1.9628
    Cell Significance Index: 150.6200
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: 1.8241
    Cell Significance Index: 26.9300
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 1.6567
    Cell Significance Index: 315.2900
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: 1.2002
    Cell Significance Index: 544.7500
  • Cell Name: microcirculation associated smooth muscle cell (CL0008035)
    Fold Change: 1.0060
    Cell Significance Index: 8.4500
  • Cell Name: supporting cell (CL0000630)
    Fold Change: 0.9050
    Cell Significance Index: 4.1800
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.7859
    Cell Significance Index: 429.1800
  • Cell Name: kidney interstitial cell (CL1000500)
    Fold Change: 0.7407
    Cell Significance Index: 5.5500
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: 0.5943
    Cell Significance Index: 61.8800
  • Cell Name: smooth muscle cell of prostate (CL1000487)
    Fold Change: 0.5785
    Cell Significance Index: 6.6900
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.5155
    Cell Significance Index: 83.8400
  • Cell Name: mesothelial cell of epicardium (CL0011019)
    Fold Change: 0.3324
    Cell Significance Index: 2.8800
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: 0.2160
    Cell Significance Index: 10.1500
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: 0.1855
    Cell Significance Index: 3.1100
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.1817
    Cell Significance Index: 17.9700
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.1288
    Cell Significance Index: 242.4900
  • Cell Name: granulosa cell (CL0000501)
    Fold Change: 0.1221
    Cell Significance Index: 3.2100
  • Cell Name: chondroblast (CL0000058)
    Fold Change: 0.1158
    Cell Significance Index: 0.6800
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: 0.0715
    Cell Significance Index: 8.3300
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.0387
    Cell Significance Index: 4.7600
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.0322
    Cell Significance Index: 14.2200
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.0045
    Cell Significance Index: 0.3100
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: -0.0070
    Cell Significance Index: -4.4800
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: -0.0200
    Cell Significance Index: -30.7700
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: -0.0211
    Cell Significance Index: -38.9700
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: -0.0253
    Cell Significance Index: -0.7300
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: -0.0292
    Cell Significance Index: -0.7300
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: -0.0326
    Cell Significance Index: -5.8700
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0346
    Cell Significance Index: -25.6600
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0428
    Cell Significance Index: -26.7500
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: -0.0441
    Cell Significance Index: -59.9800
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0471
    Cell Significance Index: -35.6400
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0496
    Cell Significance Index: -36.3400
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.0546
    Cell Significance Index: -1.9200
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: -0.0579
    Cell Significance Index: -20.7900
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0619
    Cell Significance Index: -34.9200
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: -0.0731
    Cell Significance Index: -14.6600
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: -0.0805
    Cell Significance Index: -3.6500
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.0996
    Cell Significance Index: -2.5600
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: -0.1201
    Cell Significance Index: -23.8400
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.1382
    Cell Significance Index: -17.8600
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.1440
    Cell Significance Index: -41.4300
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.1606
    Cell Significance Index: -3.4800
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.1657
    Cell Significance Index: -28.2900
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.1705
    Cell Significance Index: -24.7900
  • Cell Name: fallopian tube secretory epithelial cell (CL4030006)
    Fold Change: -0.1713
    Cell Significance Index: -2.6500
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.1817
    Cell Significance Index: -18.5600
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.1942
    Cell Significance Index: -40.9100
  • Cell Name: ovarian surface epithelial cell (CL2000064)
    Fold Change: -0.2231
    Cell Significance Index: -1.0800
  • Cell Name: fetal cardiomyocyte (CL0002495)
    Fold Change: -0.2617
    Cell Significance Index: -0.7500
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.2677
    Cell Significance Index: -19.9600
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: -0.2680
    Cell Significance Index: -16.0900
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.2809
    Cell Significance Index: -32.1800
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: -0.2971
    Cell Significance Index: -19.1700
  • Cell Name: pancreatic endocrine cell (CL0008024)
    Fold Change: -0.3256
    Cell Significance Index: -37.1700
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: -0.3297
    Cell Significance Index: -23.3200
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.3321
    Cell Significance Index: -39.1700
  • Cell Name: embryonic fibroblast (CL2000042)
    Fold Change: -0.3449
    Cell Significance Index: -1.6500
  • Cell Name: basal-myoepithelial cell of mammary gland (CL0002324)
    Fold Change: -0.3600
    Cell Significance Index: -2.6700
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.3600
    Cell Significance Index: -11.5300
  • Cell Name: fibroblast of breast (CL4006000)
    Fold Change: -0.3880
    Cell Significance Index: -2.4400
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.4442
    Cell Significance Index: -27.3000
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: -0.4584
    Cell Significance Index: -15.9300
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.4836
    Cell Significance Index: -38.3000
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.5187
    Cell Significance Index: -14.8000
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.5501
    Cell Significance Index: -25.6500
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.5880
    Cell Significance Index: -36.0500
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: -0.5936
    Cell Significance Index: -16.5900
  • Cell Name: muscle cell (CL0000187)
    Fold Change: -0.6319
    Cell Significance Index: -6.0500
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: -0.6483
    Cell Significance Index: -43.5900
  • Cell Name: fibro/adipogenic progenitor cell (CL0009099)
    Fold Change: -0.6851
    Cell Significance Index: -34.6300
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: -0.7194
    Cell Significance Index: -45.3400
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -0.7444
    Cell Significance Index: -38.6700
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: -0.7472
    Cell Significance Index: -39.2300
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.7527
    Cell Significance Index: -42.2400
  • Cell Name: preadipocyte (CL0002334)
    Fold Change: -0.7916
    Cell Significance Index: -15.4500
  • Cell Name: neuron associated cell (CL0000095)
    Fold Change: -0.7970
    Cell Significance Index: -32.6600
  • Cell Name: regular ventricular cardiac myocyte (CL0002131)
    Fold Change: -0.8220
    Cell Significance Index: -10.5400

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. **Structural homology:** TPM2 shares significant structural homology with tropomyosin alpha chain, with a conserved coiled-coil domain that interacts with actin filaments. 2. **Diversity of expression:** TPM2 is widely expressed in various cell types, including muscle cells, smooth muscle cells, and non-muscle cells, such as fibroblasts and epithelial cells. 3. **Regulatory function:** TPM2 regulates the interaction between actin and myosin, modulating muscle contraction, motility, and cell shape. 4. **Evolutionary conservation:** TPM2 is highly conserved across species, suggesting its essential role in maintaining cellular homeostasis. **Pathways and Functions:** 1. **Muscle contraction:** TPM2 regulates the interaction between actin and myosin, modulating muscle contraction and relaxation. 2. **Actin filament organization:** TPM2 interacts with actin filaments, regulating their organization and dynamics. 3. **Cytoskeletal organization:** TPM2 contributes to the regulation of cytoskeletal organization, influencing cell shape, motility, and signaling. 4. **Signaling pathways:** TPM2 interacts with various signaling molecules, including myosin light chain kinase (MLCK) and protein kinase C (PKC), modulating cell signaling and response to extracellular stimuli. **Clinical Significance:** 1. **Muscle disorders:** TPM2 mutations have been associated with various muscle disorders, including muscular dystrophy and myositis. 2. **Smooth muscle dysfunction:** TPM2 dysregulation has been implicated in smooth muscle dysfunction, leading to conditions such as hypertension and atherosclerosis. 3. **Cancer and metastasis:** TPM2 expression has been linked to cancer progression and metastasis, highlighting its potential as a therapeutic target. 4. **Neurological disorders:** TPM2 has been implicated in neurological disorders, including Alzheimer's disease and Parkinson's disease, where it regulates actin filament dynamics and cytoskeletal organization. In conclusion, TPM2 is a multifaceted protein that plays a critical role in various cellular processes, including muscle contraction, cytoskeletal organization, and cell signaling. Its dysregulation has been implicated in various diseases, including muscle disorders, smooth muscle dysfunction, cancer, and neurological disorders. Further research is needed to elucidate the complex mechanisms underlying TPM2 function and to explore its therapeutic potential.

Genular Protein ID: 3449325580

Symbol: TPM2_HUMAN

Name: Tropomyosin beta chain

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 3865200

Title: A muscle-type tropomyosin in human fibroblasts: evidence for expression by an alternative RNA splicing mechanism.

PubMed ID: 3865200

DOI: 10.1073/pnas.82.23.7835

PubMed ID: 3368322

Title: Complete nucleotide sequence of the adult skeletal isoform of human skeletal muscle beta-tropomyosin.

PubMed ID: 3368322

DOI: 10.1093/nar/16.7.3109

PubMed ID: 2059197

Title: A cDNA encoding a muscle-type tropomyosin cloned from a human epithelial cell line: identity with human fibroblast tropomyosin TM1.

PubMed ID: 2059197

DOI: 10.1016/0006-291x(91)90647-p

PubMed ID: 15164053

Title: DNA sequence and analysis of human chromosome 9.

PubMed ID: 15164053

DOI: 10.1038/nature02465

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: 2303454

Title: A nonmuscle tropomyosin is encoded by the smooth/skeletal beta-tropomyosin gene and its RNA is transcribed from an internal promoter.

PubMed ID: 2303454

DOI: 10.1016/s0021-9258(19)39791-1

PubMed ID: 11840567

Title: Cluster analysis of an extensive human breast cancer cell line protein expression map database.

PubMed ID: 11840567

DOI: 10.1002/1615-9861(200202)2:2<212::aid-prot212>3.0.co;2-h

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

PubMed ID: 11738357

Title: Mutations in the beta-tropomyosin (TPM2) gene -- a rare cause of nemaline myopathy.

PubMed ID: 11738357

DOI: 10.1016/s0960-8966(01)00252-8

PubMed ID: 12592607

Title: Mutations in genes encoding fast-twitch contractile proteins cause distal arthrogryposis syndromes.

PubMed ID: 12592607

DOI: 10.1086/368294

PubMed ID: 17846275

Title: Congenital myopathy with nemaline rods and cap structures caused by a mutation in the beta-tropomyosin gene (TPM2).

PubMed ID: 17846275

DOI: 10.1001/archneur.64.9.1334

PubMed ID: 17339586

Title: Distal arthrogryposis and muscle weakness associated with a beta-tropomyosin mutation.

PubMed ID: 17339586

DOI: 10.1212/01.wnl.0000256339.40667.fb

PubMed ID: 17434307

Title: Cap disease caused by heterozygous deletion of the beta-tropomyosin gene TPM2.

PubMed ID: 17434307

DOI: 10.1016/j.nmd.2007.02.015

PubMed ID: 19047562

Title: New morphologic and genetic findings in cap disease associated with beta-tropomyosin (TPM2) mutations.

PubMed ID: 19047562

DOI: 10.1212/01.wnl.0000336654.44814.b8

PubMed ID: 19345583

Title: Cap disease due to mutation of the beta-tropomyosin gene (TPM2).

PubMed ID: 19345583

DOI: 10.1016/j.nmd.2009.03.003

PubMed ID: 23678273

Title: First Korean family with a mutation in TPM2 associated with Sheldon-Hall syndrome.

PubMed ID: 23678273

DOI: 10.3346/jkms.2013.28.5.780

PubMed ID: 24692096

Title: Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies.

PubMed ID: 24692096

DOI: 10.1002/humu.22554

PubMed ID: 30285720

Title: Novel mutations in TPM2 and PIEZO2 are responsible for distal arthrogryposis (DA) 2B and mild DA in two Chinese families.

PubMed ID: 30285720

DOI: 10.1186/s12881-018-0692-8

Sequence Information:

  • Length: 284
  • Mass: 32851
  • Checksum: 18E330568E14E0BE
  • Sequence:
  • MDAIKKKMQM LKLDKENAID RAEQAEADKK QAEDRCKQLE EEQQALQKKL KGTEDEVEKY 
    SESVKEAQEK LEQAEKKATD AEADVASLNR RIQLVEEELD RAQERLATAL QKLEEAEKAA 
    DESERGMKVI ENRAMKDEEK MELQEMQLKE AKHIAEDSDR KYEEVARKLV ILEGELERSE 
    ERAEVAESKC GDLEEELKIV TNNLKSLEAQ ADKYSTKEDK YEEEIKLLEE KLKEAETRAE 
    FAERSVAKLE KTIDDLEDEV YAQKMKYKAI SEELDNALND ITSL

Genular Protein ID: 6141089

Symbol: A7XZE4_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15164053

Title: DNA sequence and analysis of human chromosome 9.

PubMed ID: 15164053

DOI: 10.1038/nature02465

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

Sequence Information:

  • Length: 284
  • Mass: 33026
  • Checksum: C1D4A215BBA197C1
  • Sequence:
  • MDAIKKKMQM LKLDKENAID RAEQAEADKK QAEDRCKQLE EEQQALQKKL KGTEDEVEKY 
    SESVKEAQEK LEQAEKKATD AEADVASLNR RIQLVEEELD RAQERLATAL QKLEEAEKAA 
    DESERGMKVI ENRAMKDEEK MELQEMQLKE AKHIAEDSDR KYEEVARKLV ILEGELERSE 
    ERAEVAESRA RQLEEELRTM DQALKSLMAS EEEYSTKEDK YEEEIKLLEE KLKEAETRAE 
    FAERSVAKLE KTIDDLEDEV YAQKMKYKAI SEELDNALND ITSL

Genular Protein ID: 3517933103

Symbol: Q5TCU3_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15164053

Title: DNA sequence and analysis of human chromosome 9.

PubMed ID: 15164053

DOI: 10.1038/nature02465

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

Sequence Information:

  • Length: 284
  • Mass: 32815
  • Checksum: 817AF2EB91639EB5
  • Sequence:
  • MDAIKKKMQM LKLDKENAID RAEQAEADKK QAEDRCKQLE EEQQALQKKL KGTEDEVEKY 
    SESVKEAQEK LEQAEKKATD AEADVASLNR RIQLVEEELD RAQERLATAL QKLEEAEKAA 
    DESERGMKVI ENRAMKDEEK MELQEMQLKE AKHIAEDSDR KYEEVARKLV ILEGELERSE 
    ERAEVAESKC GDLEEELKIV TNNLKSLEAQ ADKYSTKEDK YEEEIKLLEE KLKEAETRAE 
    FAERSVAKLE KTIDDLEETL ASAKEENVEI HQTLDQTLLE LNNL

Genular Protein ID: 476369656

Symbol: V9HW25_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Sequence Information:

  • Length: 284
  • Mass: 32990
  • Checksum: 584D60A8A4D6E9CA
  • Sequence:
  • MDAIKKKMQM LKLDKENAID RAEQAEADKK QAEDRCKQLE EEQQALQKKL KGTEDEVEKY 
    SESVKEAQEK LEQAEKKATD AEADVASLNR RIQLVEEELD RAQERLATAL QKLEEAEKAA 
    DESERGMKVI ENRAMKDEEK MELQEMQLKE AKHIAEDSDR KYEEVARKLV ILEGELERSE 
    ERAEVAESRA RQLEEELRTM DQALKSLMAS EEEYSTKEDK YEEEIKLLEE KLKEAETRAE 
    FAERSVAKLE KTIDDLEETL ASAKEENVEI HQTLDQTLLE LNNL

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.