Details for: SCN1B

Gene ID: 6324

Symbol: SCN1B

Ensembl ID: ENSG00000105711

Description: sodium voltage-gated channel beta subunit 1

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: 122.2474
    Cell Significance Index: -19.0200
  • Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 73.7847
    Cell Significance Index: -18.7200
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 36.3563
    Cell Significance Index: -14.7700
  • Cell Name: peripheral blood mononuclear cell (CL2000001)
    Fold Change: 35.1293
    Cell Significance Index: -18.0700
  • Cell Name: ciliated cell of the bronchus (CL0002332)
    Fold Change: 15.5644
    Cell Significance Index: -14.8600
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 15.4223
    Cell Significance Index: -19.0200
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 4.8225
    Cell Significance Index: -19.0300
  • Cell Name: type II muscle cell (CL0002212)
    Fold Change: 3.0313
    Cell Significance Index: 48.9100
  • Cell Name: type I muscle cell (CL0002211)
    Fold Change: 2.7132
    Cell Significance Index: 66.2000
  • Cell Name: cone retinal bipolar cell (CL0000752)
    Fold Change: 2.3846
    Cell Significance Index: 18.3800
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: 1.9690
    Cell Significance Index: 103.3800
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: 1.6254
    Cell Significance Index: 99.6500
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: 1.3087
    Cell Significance Index: 68.1700
  • Cell Name: leptomeningeal cell (CL0000708)
    Fold Change: 0.6781
    Cell Significance Index: 14.5000
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.6118
    Cell Significance Index: 122.7300
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.5911
    Cell Significance Index: 112.4800
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: 0.5517
    Cell Significance Index: 17.6700
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: 0.3303
    Cell Significance Index: 22.2100
  • Cell Name: L6 intratelencephalic projecting glutamatergic neuron of the primary motor cortex (CL4023050)
    Fold Change: 0.3268
    Cell Significance Index: 4.3600
  • Cell Name: endothelial cell of venule (CL1000414)
    Fold Change: 0.2922
    Cell Significance Index: 3.3200
  • Cell Name: Hofbauer cell (CL3000001)
    Fold Change: 0.2318
    Cell Significance Index: 1.8900
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 0.2091
    Cell Significance Index: 188.7800
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: 0.2060
    Cell Significance Index: 3.5300
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.1850
    Cell Significance Index: 66.3500
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: 0.1663
    Cell Significance Index: 3.5300
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.1616
    Cell Significance Index: 15.9900
  • Cell Name: OFF midget ganglion cell (CL4033047)
    Fold Change: 0.1251
    Cell Significance Index: 1.5600
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 0.1124
    Cell Significance Index: 6.7500
  • Cell Name: intestinal crypt stem cell of colon (CL0009043)
    Fold Change: 0.1106
    Cell Significance Index: 12.0300
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.1011
    Cell Significance Index: 16.4500
  • Cell Name: fallopian tube secretory epithelial cell (CL4030006)
    Fold Change: 0.0743
    Cell Significance Index: 1.1500
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: 0.0531
    Cell Significance Index: 3.4300
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 0.0366
    Cell Significance Index: 25.3500
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: 0.0238
    Cell Significance Index: 2.7700
  • Cell Name: microfold cell of epithelium of small intestine (CL1000353)
    Fold Change: 0.0169
    Cell Significance Index: 1.1700
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: -0.0012
    Cell Significance Index: -2.2000
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0052
    Cell Significance Index: -3.8800
  • Cell Name: enterocyte of epithelium of small intestine (CL1000334)
    Fold Change: -0.0056
    Cell Significance Index: -0.1600
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0061
    Cell Significance Index: -3.8200
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0066
    Cell Significance Index: -3.7400
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.0105
    Cell Significance Index: -0.3700
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: -0.0111
    Cell Significance Index: -20.4800
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: -0.0116
    Cell Significance Index: -15.8400
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: -0.0117
    Cell Significance Index: -18.0000
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: -0.0149
    Cell Significance Index: -10.9000
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0182
    Cell Significance Index: -8.2700
  • Cell Name: enteroendocrine cell of small intestine (CL0009006)
    Fold Change: -0.0220
    Cell Significance Index: -0.5500
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: -0.0231
    Cell Significance Index: -17.5100
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: -0.0243
    Cell Significance Index: -15.4100
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: -0.0261
    Cell Significance Index: -14.2300
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: -0.0285
    Cell Significance Index: -12.5900
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.0301
    Cell Significance Index: -6.3400
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: -0.0332
    Cell Significance Index: -1.5500
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: -0.0340
    Cell Significance Index: -6.7500
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0340
    Cell Significance Index: -5.8000
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: -0.0446
    Cell Significance Index: -2.0200
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.0463
    Cell Significance Index: -4.7300
  • Cell Name: ON midget ganglion cell (CL4033046)
    Fold Change: -0.0491
    Cell Significance Index: -0.6200
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.0529
    Cell Significance Index: -15.2200
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: -0.0568
    Cell Significance Index: -1.2300
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: -0.0610
    Cell Significance Index: -11.0000
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: -0.0757
    Cell Significance Index: -10.4000
  • Cell Name: fibroblast of mammary gland (CL0002555)
    Fold Change: -0.0767
    Cell Significance Index: -2.2000
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.0915
    Cell Significance Index: -13.3100
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: -0.0919
    Cell Significance Index: -7.0600
  • Cell Name: VIP GABAergic cortical interneuron (CL4023016)
    Fold Change: -0.1081
    Cell Significance Index: -2.1700
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: -0.1103
    Cell Significance Index: -13.5600
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: -0.1112
    Cell Significance Index: -4.9200
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: -0.1167
    Cell Significance Index: -4.4200
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: -0.1224
    Cell Significance Index: -14.4300
  • Cell Name: odontoblast (CL0000060)
    Fold Change: -0.1261
    Cell Significance Index: -16.1700
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.1280
    Cell Significance Index: -3.2900
  • Cell Name: transit amplifying cell of small intestine (CL0009012)
    Fold Change: -0.1311
    Cell Significance Index: -2.7200
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.1368
    Cell Significance Index: -3.9100
  • Cell Name: pancreatic endocrine cell (CL0008024)
    Fold Change: -0.1373
    Cell Significance Index: -15.6700
  • Cell Name: lactocyte (CL0002325)
    Fold Change: -0.1376
    Cell Significance Index: -17.7800
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.1721
    Cell Significance Index: -3.6700
  • Cell Name: retinal bipolar neuron (CL0000748)
    Fold Change: -0.1741
    Cell Significance Index: -2.1100
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.1745
    Cell Significance Index: -19.9900
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.1794
    Cell Significance Index: -18.6800
  • Cell Name: retinal ganglion cell (CL0000740)
    Fold Change: -0.1835
    Cell Significance Index: -1.5200
  • Cell Name: vascular lymphangioblast (CL0005022)
    Fold Change: -0.1839
    Cell Significance Index: -3.2500
  • Cell Name: eukaryotic cell (CL0000255)
    Fold Change: -0.1879
    Cell Significance Index: -8.1700
  • Cell Name: lamp5 GABAergic cortical interneuron (CL4023011)
    Fold Change: -0.1935
    Cell Significance Index: -4.1800
  • Cell Name: sst GABAergic cortical interneuron (CL4023017)
    Fold Change: -0.1942
    Cell Significance Index: -3.8400
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.1977
    Cell Significance Index: -15.6600
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: -0.2307
    Cell Significance Index: -14.5400
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: -0.2382
    Cell Significance Index: -17.7500
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.2458
    Cell Significance Index: -7.8300
  • Cell Name: photoreceptor cell (CL0000210)
    Fold Change: -0.2460
    Cell Significance Index: -3.4600
  • Cell Name: fibro/adipogenic progenitor cell (CL0009099)
    Fold Change: -0.2509
    Cell Significance Index: -12.6800
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: -0.2516
    Cell Significance Index: -7.0300
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.2520
    Cell Significance Index: -15.4900
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: -0.2547
    Cell Significance Index: -11.9700
  • Cell Name: L5 extratelencephalic projecting glutamatergic cortical neuron (CL4023041)
    Fold Change: -0.2669
    Cell Significance Index: -9.3500
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: -0.3105
    Cell Significance Index: -16.1300
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.3213
    Cell Significance Index: -18.0300
  • Cell Name: chandelier pvalb GABAergic cortical interneuron (CL4023036)
    Fold Change: -0.3217
    Cell Significance Index: -6.7200
  • Cell Name: neuron associated cell (CL0000095)
    Fold Change: -0.3337
    Cell Significance Index: -13.6700
  • Cell Name: keratocyte (CL0002363)
    Fold Change: -0.3925
    Cell Significance Index: -6.2300

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. **Gene Expression**: SCN1B is highly expressed in neuroendocrine cells, retinal ganglion cells, and cardiac muscle cells, suggesting its critical role in these cell types. 2. **Voltage-Gated Sodium Channel Subunit**: SCN1B is a beta subunit of voltage-gated sodium channels, which are essential for the generation and propagation of action potentials in neurons and cardiac muscle cells. 3. **Multiple Pathways and Functions**: SCN1B is involved in various physiological processes, including axon guidance, cell adhesion, sensory perception, and cardiac conduction. 4. **Conservation across Species**: SCN1B is conserved across species, suggesting its evolutionary significance and importance in maintaining normal cellular function. **Pathways and Functions** 1. **Axon Guidance**: SCN1B plays a critical role in axon guidance, particularly in the development of the nervous system. 2. **Cardiac Conduction**: SCN1B is involved in the regulation of cardiac conduction, including the generation and propagation of action potentials in cardiac muscle cells. 3. **Sensory Perception**: SCN1B is expressed in sensory neurons and is involved in the perception of sweet, bitter, and umami tastes. 4. **Neuronal Action Potential Propagation**: SCN1B regulates the propagation of action potentials in neurons, ensuring proper neuronal function. 5. **Cell Adhesion**: SCN1B interacts with L1cam and ankyrins, influencing cell adhesion and migration. **Clinical Significance** 1. **Neurological Disorders**: Alterations in SCN1B expression have been linked to various neurological disorders, including epilepsy, migraines, and neurodegenerative diseases. 2. **Cardiac Disorders**: SCN1B is also involved in cardiac disorders, including arrhythmias and cardiac conduction defects. 3. **Taste Disorders**: SCN1B mutations have been associated with taste disorders, including impaired sweet, bitter, and umami taste perception. 4. **Therapeutic Implications**: Understanding the role of SCN1B in various physiological processes and disorders has implications for the development of novel therapeutic strategies, including targeted therapies for neurological and cardiac disorders. In conclusion, the SCN1B gene plays a critical role in maintaining normal cellular function, particularly in the development and regulation of the nervous system and cardiac conduction. Alterations in SCN1B expression have been linked to various neurological and cardiac disorders, highlighting the importance of this gene in human health and disease. Further research is needed to fully elucidate the mechanisms underlying SCN1B function and its clinical significance.

Genular Protein ID: 1634978912

Symbol: SCN1B_HUMAN

Name: N/A

UniProtKB Accession Codes:

Q07699 Q5TZZ4 Q6TN97

Database IDs:

AGR 1 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 BindingDB 1 BioGRID 1 BioGRID-ORCS 1 BioMuta 1 CCDS 2 CTD 1 ChEMBL 1 ComplexPortal 20 DMDM 1 DNASU 1 DisGeNET 1 DrugBank 9 DrugCentral 1 EMBL 13 EMDB 31 Ensembl 3 ExpressionAtlas 1 GO 31 Gene3D 1 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 4 KEGG 1 MANE-Select 1 MIM 9 MINT 1 MalaCards 1 MassIVE 1 NCBI Taxonomy 1 OMA 1 OpenTargets 1 Orphanet 6 OrthoDB 1 PANTHER 2 PDB 33 PDBsum 33 PIR 1 PRO 1 PathwayCommons 1 PaxDb 1 PeptideAtlas 1 Pfam 1 PharmGKB 1 Pharos 1 PhosphoSitePlus 1 PhylomeDB 1 Proteomes 1 ProteomicsDB 2 RNAct 1 Reactome 3 RefSeq 3 SMR 1 STRING 1 SUPFAM 1 SignaLink 1 TreeFam 1 UCSC 1 VEuPathDB 1 eggNOG 1 iPTMnet 1 neXtProt 1

Citations:

PubMed ID: 8394762

Title: The cloning and expression of a sodium channel beta 1-subunit cDNA from human brain.

PubMed ID: 8394762

DOI: 10.1093/hmg/2.6.745

PubMed ID: 8125980

Title: Voltage-gated Na+ channel beta 1 subunit mRNA expressed in adult human skeletal muscle, heart, and brain is encoded by a single gene.

PubMed ID: 8125980

DOI: 10.1016/s0021-9258(17)37325-8

PubMed ID: 7851891

Title: Genomic organization and chromosomal assignment of the human voltage-gated Na+ channel beta 1 subunit gene (SCN1B).

PubMed ID: 7851891

DOI: 10.1006/geno.1994.1551

PubMed ID: 14622265

Title: Molecular cloning and functional expression of the human sodium channel beta1B subunit, a novel splicing variant of the beta1 subunit.

PubMed ID: 14622265

DOI: 10.1046/j.1432-1033.2003.03878.x

PubMed ID: 14702039

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

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15057824

Title: The DNA sequence and biology of human chromosome 19.

PubMed ID: 15057824

DOI: 10.1038/nature02399

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: 15525788

Title: A novel epilepsy mutation in the sodium channel SCN1A identifies a cytoplasmic domain for beta subunit interaction.

PubMed ID: 15525788

DOI: 10.1523/jneurosci.2034-04.2004

PubMed ID: 18464934

Title: Sodium channel beta1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.

PubMed ID: 18464934

DOI: 10.1172/jci33891

PubMed ID: 19710327

Title: A functional null mutation of SCN1B in a patient with Dravet syndrome.

PubMed ID: 19710327

DOI: 10.1523/jneurosci.2475-09.2009

PubMed ID: 21994374

Title: Voltage-gated Na+ channel beta1B: a secreted cell adhesion molecule involved in human epilepsy.

PubMed ID: 21994374

DOI: 10.1523/jneurosci.0361-11.2011

PubMed ID: 26900580

Title: Pathogenic mechanism of recurrent mutations of SCN8A in epileptic encephalopathy.

PubMed ID: 26900580

DOI: 10.1002/acn3.276

PubMed ID: 29992740

Title: A mutation of SCN1B associated with GEFS+ causes functional and maturation defects of the voltage-dependent sodium channel.

PubMed ID: 29992740

DOI: 10.1002/humu.23589

PubMed ID: 30190309

Title: Structure of the human voltage-gated sodium channel Nav1.4 in complex with beta1.

PubMed ID: 30190309

DOI: 10.1126/science.aau2486

PubMed ID: 30765606

Title: Structures of human Nav1.7 channel in complex with auxiliary subunits and animal toxins.

PubMed ID: 30765606

DOI: 10.1126/science.aaw2493

PubMed ID: 35277491

Title: Structural basis for modulation of human NaV1.3 by clinical drug and selective antagonist.

PubMed ID: 35277491

DOI: 10.1038/s41467-022-28808-5

PubMed ID: 36823201

Title: Structure of human NaV1.6 channel reveals Na+ selectivity and pore blockade by 4,9-anhydro-tetrodotoxin.

PubMed ID: 36823201

DOI: 10.1038/s41467-023-36766-9

PubMed ID: 36696443

Title: Cryo-EM structure of human voltage-gated sodium channel Nav1.6.

PubMed ID: 36696443

DOI: 10.1073/pnas.2220578120

PubMed ID: 9697698

Title: Febrile seizures and generalized epilepsy associated with a mutation in the Na(+)-channel beta-1 subunit gene SCN1B.

PubMed ID: 9697698

DOI: 10.1038/1252

PubMed ID: 17928445

Title: Modulatory proteins can rescue a trafficking defective epileptogenic Nav1.1 Na+ channel mutant.

PubMed ID: 17928445

DOI: 10.1523/jneurosci.3515-07.2007

PubMed ID: 19808477

Title: Mutations in sodium channel beta1- and beta2-subunits associated with atrial fibrillation.

PubMed ID: 19808477

DOI: 10.1161/circep.108.779181

PubMed ID: 19522081

Title: Mutational analysis of the SCN1A, SCN1B and GABRG2 genes in 150 Italian patients with idiopathic childhood epilepsies.

PubMed ID: 19522081

DOI: 10.1111/j.1399-0004.2009.01155.x

PubMed ID: 21040232

Title: New mutation c.374C>T and a putative disease-associated haplotype within SCN1B gene in Tunisian families with febrile seizures.

PubMed ID: 21040232

DOI: 10.1111/j.1468-1331.2010.03216.x

PubMed ID: 23148524

Title: A homozygous mutation of voltage-gated sodium channel beta(I) gene SCN1B in a patient with Dravet syndrome.

PubMed ID: 23148524

DOI: 10.1111/epi.12040

Sequence Information:

  • Length: 218
  • Mass: 24707
  • Checksum: 09B812FA3F9E9018
  • Sequence:
    • MGRLLALVVG AALVSSACGG CVEVDSETEA VYGMTFKILC ISCKRRSETN AETFTEWTFR 
QKGTEEFVKI LRYENEVLQL EEDERFEGRV VWNGSRGTKD LQDLSIFITN VTYNHSGDYE 
CHVYRLLFFE NYEHNTSVVK KIHIEVVDKA NRDMASIVSE IMMYVLIVVL TIWLVAEMIY 
CYKKIAAATE TAAQENASEY LAITSESKEN CTGVQVAE

Genular Protein ID: 1575660461

Symbol: A0A1W2PR05_HUMAN

Name: N/A

UniProtKB Accession Codes:

A0A1W2PR05

Database IDs:

ARBA 12 AlphaFoldDB 1 Antibodypedia 1 Bgee 1 CTD 1 DNASU 1 DisGeNET 1 EMBL 1 Ensembl 2 ExpressionAtlas 1 GO 5 Gene3D 1 GeneTree 1 HGNC 1 InterPro 4 MassIVE 1 NCBI Taxonomy 1 OrthoDB 1 PANTHER 2 PeptideAtlas 2 Pfam 2 Proteomes 2 ProteomicsDB 1 RefSeq 1 SAM 1 SMR 1 SUPFAM 1 VEuPathDB 1

Citations:

PubMed ID: 11237011

Title: Initial sequencing and analysis of the human genome.

PubMed ID: 11237011

DOI: 10.1038/35057062

PubMed ID: 15057824

Title: The DNA sequence and biology of human chromosome 19.

PubMed ID: 15057824

DOI: 10.1038/nature02399

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

Sequence Information:

  • Length: 185
  • Mass: 21497
  • Checksum: CFE5B8510DC59800
  • Sequence:
    • MTFKILCISC KRRSETNAET FTEWTFRQKG TEEFVKILRY ENEVLQLEED ERFEGRVVWN 
GSRGTKDLQD LSIFITNVTY NHSGDYECHV YRLLFFENYE HNTSVVKKIH IEVVDKANRD 
MASIVSEIMM YVLIVVLTIW LVAEMIYCYK KIAAATETAA QENASEYLAI TSESKENCTG 
VQVAE

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.