Details for: UROS

Gene ID: 7390

Symbol: UROS

Ensembl ID: ENSG00000188690

Description: uroporphyrinogen III synthase

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: hematopoietic oligopotent progenitor cell (CL0002032)
    Fold Change: 101.2839
    Cell Significance Index: -25.6900
  • Cell Name: smooth muscle fiber of ileum (CL1000278)
    Fold Change: 77.1410
    Cell Significance Index: -36.4200
  • Cell Name: mucosal type mast cell (CL0000485)
    Fold Change: 73.7464
    Cell Significance Index: -29.9600
  • Cell Name: peripheral blood mononuclear cell (CL2000001)
    Fold Change: 65.1846
    Cell Significance Index: -33.5300
  • Cell Name: ileal goblet cell (CL1000326)
    Fold Change: 54.4542
    Cell Significance Index: -36.5400
  • Cell Name: polychromatophilic erythroblast (CL0000550)
    Fold Change: 33.3665
    Cell Significance Index: -5.1900
  • Cell Name: ciliated cell of the bronchus (CL0002332)
    Fold Change: 31.4744
    Cell Significance Index: -30.0500
  • Cell Name: orthochromatic erythroblast (CL0000552)
    Fold Change: 24.5913
    Cell Significance Index: -30.3200
  • Cell Name: CD8-alpha-beta-positive, alpha-beta intraepithelial T cell (CL0000796)
    Fold Change: 9.4219
    Cell Significance Index: -25.2400
  • Cell Name: stromal cell of bone marrow (CL0010001)
    Fold Change: 9.2371
    Cell Significance Index: -36.4500
  • Cell Name: CD8-positive, alpha-beta regulatory T cell (CL0000795)
    Fold Change: 8.1818
    Cell Significance Index: -25.1300
  • Cell Name: granulosa cell (CL0000501)
    Fold Change: 1.6062
    Cell Significance Index: 42.2400
  • Cell Name: gut absorptive cell (CL0000677)
    Fold Change: 1.5101
    Cell Significance Index: 90.6600
  • Cell Name: acinar cell of salivary gland (CL0002623)
    Fold Change: 1.2920
    Cell Significance Index: 60.2400
  • Cell Name: glycinergic neuron (CL1001509)
    Fold Change: 1.0641
    Cell Significance Index: 55.8700
  • Cell Name: epithelial cell of stomach (CL0002178)
    Fold Change: 1.0489
    Cell Significance Index: 122.2400
  • Cell Name: tuft cell of colon (CL0009041)
    Fold Change: 1.0109
    Cell Significance Index: 912.7400
  • Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
    Fold Change: 0.8963
    Cell Significance Index: 179.8000
  • Cell Name: conjunctival epithelial cell (CL1000432)
    Fold Change: 0.8392
    Cell Significance Index: 11.4500
  • Cell Name: epithelial cell of small intestine (CL0002254)
    Fold Change: 0.6300
    Cell Significance Index: 102.4700
  • Cell Name: cell in vitro (CL0001034)
    Fold Change: 0.5620
    Cell Significance Index: 306.9200
  • Cell Name: stromal cell of ovary (CL0002132)
    Fold Change: 0.5493
    Cell Significance Index: 75.4400
  • Cell Name: eye photoreceptor cell (CL0000287)
    Fold Change: 0.5076
    Cell Significance Index: 31.9900
  • Cell Name: early pro-B cell (CL0002046)
    Fold Change: 0.5008
    Cell Significance Index: 32.3100
  • Cell Name: paneth cell of epithelium of small intestine (CL1000343)
    Fold Change: 0.4740
    Cell Significance Index: 10.2700
  • Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
    Fold Change: 0.4177
    Cell Significance Index: 149.8300
  • Cell Name: intermediate cell of urothelium (CL4030055)
    Fold Change: 0.3752
    Cell Significance Index: 67.6400
  • Cell Name: neoplastic cell (CL0001063)
    Fold Change: 0.3689
    Cell Significance Index: 73.2100
  • Cell Name: tonsil germinal center B cell (CL2000006)
    Fold Change: 0.3194
    Cell Significance Index: 37.6700
  • Cell Name: basal cell of urothelium (CL1000486)
    Fold Change: 0.3077
    Cell Significance Index: 37.8400
  • Cell Name: odontoblast (CL0000060)
    Fold Change: 0.2909
    Cell Significance Index: 37.2900
  • Cell Name: indirect pathway medium spiny neuron (CL4023029)
    Fold Change: 0.2901
    Cell Significance Index: 12.8300
  • Cell Name: direct pathway medium spiny neuron (CL4023026)
    Fold Change: 0.2501
    Cell Significance Index: 9.4700
  • Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
    Fold Change: 0.2201
    Cell Significance Index: 6.1500
  • Cell Name: hair follicular keratinocyte (CL2000092)
    Fold Change: 0.2180
    Cell Significance Index: 96.3800
  • Cell Name: lactocyte (CL0002325)
    Fold Change: 0.2156
    Cell Significance Index: 27.8500
  • Cell Name: fibroblast of dermis (CL0002551)
    Fold Change: 0.1978
    Cell Significance Index: 4.1400
  • Cell Name: CD4-positive, alpha-beta memory T cell, CD45RO-positive (CL0001204)
    Fold Change: 0.1716
    Cell Significance Index: 5.0400
  • Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
    Fold Change: 0.1540
    Cell Significance Index: 7.2400
  • Cell Name: bladder urothelial cell (CL1001428)
    Fold Change: 0.1536
    Cell Significance Index: 7.9800
  • Cell Name: enterocyte of epithelium of large intestine (CL0002071)
    Fold Change: 0.1513
    Cell Significance Index: 6.8600
  • Cell Name: sebum secreting cell (CL0000317)
    Fold Change: 0.1292
    Cell Significance Index: 9.1400
  • Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
    Fold Change: 0.1245
    Cell Significance Index: 4.3300
  • Cell Name: GABAergic interneuron (CL0011005)
    Fold Change: 0.1236
    Cell Significance Index: 85.4700
  • Cell Name: enteroendocrine cell of colon (CL0009042)
    Fold Change: 0.0994
    Cell Significance Index: 18.9100
  • Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
    Fold Change: 0.0668
    Cell Significance Index: 4.9800
  • Cell Name: cardiac muscle myoblast (CL0000513)
    Fold Change: 0.0513
    Cell Significance Index: 3.9400
  • Cell Name: retinal rod cell (CL0000604)
    Fold Change: 0.0495
    Cell Significance Index: 0.5900
  • Cell Name: pigmented epithelial cell (CL0000529)
    Fold Change: 0.0481
    Cell Significance Index: 90.5100
  • Cell Name: microcirculation associated smooth muscle cell (CL0008035)
    Fold Change: 0.0298
    Cell Significance Index: 0.2500
  • Cell Name: colon goblet cell (CL0009039)
    Fold Change: 0.0269
    Cell Significance Index: 2.6600
  • Cell Name: secondary lens fiber (CL0002225)
    Fold Change: 0.0193
    Cell Significance Index: 26.2300
  • Cell Name: anterior lens cell (CL0002223)
    Fold Change: 0.0069
    Cell Significance Index: 12.7700
  • Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
    Fold Change: 0.0062
    Cell Significance Index: 4.5300
  • Cell Name: pulmonary alveolar epithelial cell (CL0000322)
    Fold Change: 0.0049
    Cell Significance Index: 3.6800
  • Cell Name: lens epithelial cell (CL0002224)
    Fold Change: 0.0029
    Cell Significance Index: 4.4700
  • Cell Name: mesenchymal cell (CL0008019)
    Fold Change: -0.0096
    Cell Significance Index: -0.1600
  • Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
    Fold Change: -0.0120
    Cell Significance Index: -7.6400
  • Cell Name: pancreatic acinar cell (CL0002064)
    Fold Change: -0.0252
    Cell Significance Index: -4.3100
  • Cell Name: pancreatic A cell (CL0000171)
    Fold Change: -0.0326
    Cell Significance Index: -24.1600
  • Cell Name: abnormal cell (CL0001061)
    Fold Change: -0.0346
    Cell Significance Index: -3.5300
  • Cell Name: ciliary muscle cell (CL1000443)
    Fold Change: -0.0363
    Cell Significance Index: -16.4800
  • Cell Name: type B pancreatic cell (CL0000169)
    Fold Change: -0.0446
    Cell Significance Index: -25.1300
  • Cell Name: pancreatic PP cell (CL0002275)
    Fold Change: -0.0645
    Cell Significance Index: -40.2500
  • Cell Name: peg cell (CL4033014)
    Fold Change: -0.0697
    Cell Significance Index: -1.6100
  • Cell Name: neutrophil progenitor cell (CL0000834)
    Fold Change: -0.0779
    Cell Significance Index: -2.0900
  • Cell Name: placental villous trophoblast (CL2000060)
    Fold Change: -0.0873
    Cell Significance Index: -2.3300
  • Cell Name: transit amplifying cell of colon (CL0009011)
    Fold Change: -0.0918
    Cell Significance Index: -2.9400
  • Cell Name: skeletal muscle myoblast (CL0000515)
    Fold Change: -0.0984
    Cell Significance Index: -1.0700
  • Cell Name: dopaminergic neuron (CL0000700)
    Fold Change: -0.1022
    Cell Significance Index: -29.4000
  • Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
    Fold Change: -0.1108
    Cell Significance Index: -2.3600
  • Cell Name: forebrain neuroblast (CL1000042)
    Fold Change: -0.1113
    Cell Significance Index: -6.8400
  • Cell Name: small intestine goblet cell (CL1000495)
    Fold Change: -0.1278
    Cell Significance Index: -4.4900
  • Cell Name: pigmented ciliary epithelial cell (CL0002303)
    Fold Change: -0.1328
    Cell Significance Index: -19.3100
  • Cell Name: pro-T cell (CL0000827)
    Fold Change: -0.1450
    Cell Significance Index: -3.7100
  • Cell Name: hippocampal granule cell (CL0001033)
    Fold Change: -0.1639
    Cell Significance Index: -11.0200
  • Cell Name: pancreatic ductal cell (CL0002079)
    Fold Change: -0.1657
    Cell Significance Index: -18.9800
  • Cell Name: pancreatic D cell (CL0000173)
    Fold Change: -0.1808
    Cell Significance Index: -38.0900
  • Cell Name: cerebellar granule cell (CL0001031)
    Fold Change: -0.1867
    Cell Significance Index: -3.2000
  • Cell Name: retinal progenitor cell (CL0002672)
    Fold Change: -0.2103
    Cell Significance Index: -11.8000
  • Cell Name: lung endothelial cell (CL1001567)
    Fold Change: -0.2303
    Cell Significance Index: -12.0000
  • Cell Name: hippocampal pyramidal neuron (CL1001571)
    Fold Change: -0.2449
    Cell Significance Index: -6.9900
  • Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
    Fold Change: -0.2722
    Cell Significance Index: -21.5600
  • Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
    Fold Change: -0.3314
    Cell Significance Index: -34.5100
  • Cell Name: Purkinje cell (CL0000121)
    Fold Change: -0.3594
    Cell Significance Index: -7.8700
  • Cell Name: cortical cell of adrenal gland (CL0002097)
    Fold Change: -0.4219
    Cell Significance Index: -11.3100
  • Cell Name: umbrella cell of urothelium (CL4030056)
    Fold Change: -0.4870
    Cell Significance Index: -4.4900
  • Cell Name: endothelial cell of venule (CL1000414)
    Fold Change: -0.5290
    Cell Significance Index: -6.0100
  • Cell Name: pvalb GABAergic cortical interneuron (CL4023018)
    Fold Change: -0.5654
    Cell Significance Index: -12.0000
  • Cell Name: melanocyte of skin (CL1000458)
    Fold Change: -0.5847
    Cell Significance Index: -8.2000
  • Cell Name: intestinal tuft cell (CL0019032)
    Fold Change: -0.6002
    Cell Significance Index: -36.8000
  • Cell Name: GABAergic amacrine cell (CL4030027)
    Fold Change: -0.6023
    Cell Significance Index: -7.4700
  • Cell Name: basal cell of prostate epithelium (CL0002341)
    Fold Change: -0.6121
    Cell Significance Index: -16.6600
  • Cell Name: skeletal muscle fiber (CL0008002)
    Fold Change: -0.6158
    Cell Significance Index: -15.8300
  • Cell Name: cardiac muscle cell (CL0000746)
    Fold Change: -0.6408
    Cell Significance Index: -9.4600
  • Cell Name: cortical interneuron (CL0008031)
    Fold Change: -0.6684
    Cell Significance Index: -16.0300
  • Cell Name: corticothalamic-projecting glutamatergic cortical neuron (CL4023013)
    Fold Change: -0.6864
    Cell Significance Index: -21.8600
  • Cell Name: kidney epithelial cell (CL0002518)
    Fold Change: -0.7021
    Cell Significance Index: -20.6800
  • Cell Name: L6b glutamatergic cortical neuron (CL4023038)
    Fold Change: -0.7074
    Cell Significance Index: -23.1600
  • Cell Name: intestinal epithelial cell (CL0002563)
    Fold Change: -0.7177
    Cell Significance Index: -7.4300

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** UROS is a cytosolic enzyme, and its expression is widespread in various cell types, including neural progenitor cells, erythroid progenitor cells, and GABAergic neurons. The UROS protein is a homodimeric enzyme, consisting of two identical subunits. The enzyme exhibits a high degree of specificity for uroporphyrinogen III synthesis, and its activity is tightly regulated by various factors, including cellular energy status, iron availability, and heme biosynthesis intermediates. **Pathways and Functions** The UROS enzyme is involved in the heme biosynthetic pathway, which is a complex network of reactions that convert ALA into heme. The UROS enzyme catalyzes the condensation of ALA and succinyl-CoA to form uroporphyrinogen III, which is then converted into coproporphyrinogen III, protoporphyrinogen IX, and ultimately, heme. The UROS enzyme also plays a role in the metabolism of porphyrins, which are key intermediates in the heme biosynthetic pathway. In addition to its role in heme biosynthesis, the UROS enzyme is also involved in the cellular response to various stimuli, including amine and arsenic-containing substances. The enzyme's activity is regulated by various signaling pathways, including the mitogen-activated protein kinase (MAPK) pathway and the phosphatidylinositol 3-kinase (PI3K) pathway. **Clinical Significance** Deficiencies in UROS have been linked to several rare genetic disorders, including congenital erythropoietic porphyria (CEP) and acute intermittent porphyria (AIP). CEP is a rare genetic disorder characterized by severe erythropoietic anemia, skin blistering, and neurological abnormalities. AIP is a rare genetic disorder characterized by acute episodes of abdominal pain, neurological symptoms, and psychiatric disturbances. The UROS enzyme's role in heme biosynthesis makes it a potential target for therapeutic interventions in these disorders. Furthermore, the UROS enzyme's involvement in cellular response to various stimuli makes it a potential target for therapeutic interventions in other diseases, including cancer and neurodegenerative disorders. The enzyme's activity is regulated by various signaling pathways, making it a potential target for modulating cellular responses to various stimuli. In conclusion, the UROS gene plays a critical role in the heme biosynthetic pathway, and its deficiency has been linked to several rare genetic disorders. Further research is needed to fully understand the UROS enzyme's role in human disease and to explore its potential as a therapeutic target.

Genular Protein ID: 435414242

Symbol: HEM4_HUMAN

Name: Uroporphyrinogen-III synthase

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 3174619

Title: Human uroporphyrinogen III synthase: molecular cloning, nucleotide sequence, and expression of a full-length cDNA.

PubMed ID: 3174619

DOI: 10.1073/pnas.85.19.7049

PubMed ID: 11112350

Title: Human uroporphyrinogen-III synthase: genomic organization, alternative promoters, and erythroid-specific expression.

PubMed ID: 11112350

DOI: 10.1006/geno.2000.6373

PubMed ID: 14702039

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

PubMed ID: 14702039

DOI: 10.1038/ng1285

PubMed ID: 15164054

Title: The DNA sequence and comparative analysis of human chromosome 10.

PubMed ID: 15164054

DOI: 10.1038/nature02462

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: 8829650

Title: Molecular basis of congenital erythropoietic porphyria: mutations in the human uroporphyrinogen III synthase gene.

PubMed ID: 8829650

DOI: 10.1002/(sici)1098-1004(1996)7:3<187::aid-humu1>3.0.co;2-8

PubMed ID: 18004775

Title: Human uroporphyrinogen III synthase: NMR-based mapping of the active site.

PubMed ID: 18004775

DOI: 10.1002/prot.21755

PubMed ID: 11689424

Title: Crystal structure of human uroporphyrinogen III synthase.

PubMed ID: 11689424

DOI: 10.1093/emboj/20.21.5832

PubMed ID: 2331520

Title: Point mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria (Gunther's disease).

PubMed ID: 2331520

PubMed ID: 1733834

Title: Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria.

PubMed ID: 1733834

DOI: 10.1007/bf00197267

PubMed ID: 1737856

Title: Congenital erythropoietic porphyria: identification and expression of exonic mutations in the uroporphyrinogen III synthase gene.

PubMed ID: 1737856

DOI: 10.1172/jci115637

PubMed ID: 7860775

Title: Congenital erythropoietic porphyria: identification and expression of 10 mutations in the uroporphyrinogen III synthase gene.

PubMed ID: 7860775

DOI: 10.1172/jci117742

PubMed ID: 8655129

Title: A novel point mutation in congenital erythropoietic porphyria in two members of Japanese family.

PubMed ID: 8655129

DOI: 10.1007/bf02281859

PubMed ID: 9188670

Title: Novel point mutation in the uroporphyrinogen III synthase gene causes congenital erythropoietic porphyria of a Japanese family.

PubMed ID: 9188670

DOI: 10.1002/(sici)1096-8628(19970613)70:3<299::aid-ajmg16>3.0.co;2-g

PubMed ID: 9834209

Title: Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation.

PubMed ID: 9834209

PubMed ID: 9803266

Title: C73R is a hotspot mutation in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria.

PubMed ID: 9803266

DOI: 10.1046/j.1469-1809.1998.6230225.x

PubMed ID: 11121156

Title: Congenital erythropoietic porphyria: a novel homozygous mutation in a Japanese patient.

PubMed ID: 11121156

DOI: 10.1046/j.1523-1747.2000.0202a.x

PubMed ID: 12060141

Title: Congenital erythropoietic porphyria: identification and expression of eight novel mutations in the uroporphyrinogen III synthase gene.

PubMed ID: 12060141

DOI: 10.1046/j.1365-2141.2002.03558.x

PubMed ID: 15304101

Title: Congenital erythropoietic porphyria: report of a novel mutation with absence of clinical manifestations in a homozygous mutant sibling.

PubMed ID: 15304101

DOI: 10.1111/j.0022-202x.2004.23401.x

PubMed ID: 21653323

Title: ALAS2 acts as a modifier gene in patients with congenital erythropoietic porphyria.

PubMed ID: 21653323

DOI: 10.1182/blood-2011-03-342873

PubMed ID: 22350154

Title: Mutational analysis of uroporphyrinogen III cosynthase gene in Iranian families with congenital erythropoietic porphyria.

PubMed ID: 22350154

DOI: 10.1007/s11033-012-1497-z

Sequence Information:

  • Length: 265
  • Mass: 28628
  • Checksum: CEF171401361F61E
  • Sequence:
  • MKVLLLKDAK EDDCGQDPYI RELGLYGLEA TLIPVLSFEF LSLPSFSEKL SHPEDYGGLI 
    FTSPRAVEAA ELCLEQNNKT EVWERSLKEK WNAKSVYVVG NATASLVSKI GLDTEGETCG 
    NAEKLAEYIC SRESSALPLL FPCGNLKREI LPKALKDKGI AMESITVYQT VAHPGIQGNL 
    NSYYSQQGVP ASITFFSPSG LTYSLKHIQE LSGDNIDQIK FAAIGPTTAR ALAAQGLPVS 
    CTAESPTPQA LATGIRKALQ PHGCC

Genular Protein ID: 3741145343

Symbol: A0A3B3ISM6_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: 15164054

Title: The DNA sequence and comparative analysis of human chromosome 10.

PubMed ID: 15164054

DOI: 10.1038/nature02462

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

Sequence Information:

  • Length: 292
  • Mass: 31662
  • Checksum: E1B2F827EDD4DD86
  • Sequence:
  • MKVLLLKDAK EDDCGQDPYI RELGLYGLEA TLIPVLSFEF LSLPSFSEKL SHPEDYGGLI 
    FTSPRAVEAA ELCLEQNNKT EVWERSLKEK WNAKSVYVVG NATASLVSKI GLDTEGETCG 
    NAEKLAEYIC SRESSALPLL FPCGNLKREI LPKALKDKGI AMESITVYQT VAHPGIQGNL 
    NSYYSQQGVP ASITFFSPSG LTYSLKHIQE LSGDNIDQIK TQGPQHPKKN CLQLEPLRKD 
    CTDTAVMFAA IGPTTARALA AQGLPVSCTA ESPTPQALAT GIRKALQPHG CC

Genular Protein ID: 358411946

Symbol: A0A0S2Z5C5_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 26871637

Title: Widespread Expansion of Protein Interaction Capabilities by Alternative Splicing.

PubMed ID: 26871637

DOI: 10.1016/j.cell.2016.01.029

Sequence Information:

  • Length: 238
  • Mass: 25707
  • Checksum: 8E6D4FAEE863CB22
  • Sequence:
  • MKVLLLKDAK EDDCGQDPYI RELGLYGLEA TLIPVLSFEF LSLPSFSEKL SHPEDYGGLI 
    FTSPRAVEAA ELCLEQNNKT EVWERSLKEK WNAKSVYVVG NATASLVSKI GLDTEGETCG 
    NAEKLAEYIC SRIAMESITV YQTVAHPGIQ GNLNSYYSQQ GVPASITFFS PSGLTYSLKH 
    IQELSGDNID QIKFAAIGPT TARALAAQGL PVSCTAESPT PQALATGIRK ALQPHGCC

Genular Protein ID: 2244467587

Symbol: A0A3B3ITJ2_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: 15164054

Title: The DNA sequence and comparative analysis of human chromosome 10.

PubMed ID: 15164054

DOI: 10.1038/nature02462

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

Sequence Information:

  • Length: 265
  • Mass: 28742
  • Checksum: 02E7367F3441EE9D
  • Sequence:
  • MKVLLLKDAK EDDCGQDPYI RELGLYGLEA TLIPVLSFEF LSLPSFSEKL SHPEDYGGLI 
    FTSPRAVEAA ELCLEQNNKT EVWERSLKEK WNAKSVYVVG NATASLVSKI GLDTEGETCG 
    NAEKLAEYIC SRIAMESITV YQTVAHPGIQ GNLNSYYSQQ GVPASITFFS PSGLTYSLKH 
    IQELSGDNID QIKTQGPQHP KKNCLQLEPL RKDCTDTAVM FAAIGPTTAR ALAAQGLPVS 
    CTAESPTPQA LATGIRKALQ PHGCC

Genular Protein ID: 305624272

Symbol: Q5T3L8_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: 11181995

Title: The sequence of the human genome.

PubMed ID: 11181995

DOI: 10.1126/science.1058040

PubMed ID: 15164054

Title: The DNA sequence and comparative analysis of human chromosome 10.

PubMed ID: 15164054

DOI: 10.1038/nature02462

PubMed ID: 15496913

Title: Finishing the euchromatic sequence of the human genome.

PubMed ID: 15496913

DOI: 10.1038/nature03001

Sequence Information:

  • Length: 139
  • Mass: 15369
  • Checksum: 473CF085DB483901
  • Sequence:
  • MKVLLLKDAK EDDCGQDPYI RELGLYGLEA TLIPVLSFEF LSLPSFSEKL SHPEDYGGLI 
    FTSPRAVEAA ELCLEQNNKT EVWERSLKEK WNAKSVYVVG NATASLVSKI GLDTEGETCG 
    NAEKLAEYIC SSEEVKGIF

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.