Details for: CL0001061

Cell ID: CL0001061

Cell Name: abnormal cell

Marker Score Threshold: 2995
(Derived using integrated single-cell and genomic data)

Description: A cell found in an organism or derived from an organism exhibiting a phenotype that deviates from the expected phenotype of any native cell type of that organism. Abnormal cells are typically found in disease states or disease models.

Genes (max top 100)

(Marker Score score is uniquely calculated using our advanced thresholding algorithms to reveal cell-specific gene markers)

  • Gene Symbol: IFNB1 (ENSG00000171855)
    Fold Change: 1.22
    Ensembl ID: ENSG00000171855
  • Gene Symbol: OR1A1 (ENSG00000172146)
    Fold Change: 1.22
    Ensembl ID: ENSG00000172146
  • Gene Symbol: FUT5 (ENSG00000130383)
    Fold Change: 1.22
    Ensembl ID: ENSG00000130383
  • Gene Symbol: IFNA10 (ENSG00000186803)
    Fold Change: 1.22
    Ensembl ID: ENSG00000186803
  • Gene Symbol: PDHA2 (ENSG00000163114)
    Fold Change: 1.22
    Ensembl ID: ENSG00000163114
  • Gene Symbol: RNY3 (ENSG00000202354)
    Fold Change: 1.22
    Ensembl ID: ENSG00000202354
  • Gene Symbol: TRGV1 (ENSG00000211701)
    Fold Change: 1.22
    Ensembl ID: ENSG00000211701
  • Gene Symbol: GAS8 AS1 (ENSG00000221819)
    Fold Change: 1.22
    Ensembl ID: ENSG00000221819
  • Gene Symbol: GJA8 (ENSG00000121634)
    Fold Change: 1.22
    Ensembl ID: ENSG00000121634
  • Gene Symbol: NPBWR2 (ENSG00000125522)
    Fold Change: 1.22
    Ensembl ID: ENSG00000125522
  • Gene Symbol: IFNA5 (ENSG00000147873)
    Fold Change: 1.22
    Ensembl ID: ENSG00000147873
  • Gene Symbol: LHB (ENSG00000104826)
    Fold Change: 1.22
    Ensembl ID: ENSG00000104826
  • Gene Symbol: TNP1 (ENSG00000118245)
    Fold Change: 1.22
    Ensembl ID: ENSG00000118245
  • Gene Symbol: H1 6 (ENSG00000187475)
    Fold Change: 1.22
    Ensembl ID: ENSG00000187475
  • Gene Symbol: INSL4 (ENSG00000120211)
    Fold Change: 1.22
    Ensembl ID: ENSG00000120211
  • Gene Symbol: PRH2 (ENSG00000134551)
    Fold Change: 1.22
    Ensembl ID: ENSG00000134551
  • Gene Symbol: IFNA21 (ENSG00000137080)
    Fold Change: 1.22
    Ensembl ID: ENSG00000137080
  • Gene Symbol: KRT31 (ENSG00000094796)
    Fold Change: 1.22
    Ensembl ID: ENSG00000094796
  • Gene Symbol: PRM1 (ENSG00000175646)
    Fold Change: 1.22
    Ensembl ID: ENSG00000175646
  • Gene Symbol: SNORD13P3 (ENSG00000239128)
    Fold Change: 1.22
    Ensembl ID: ENSG00000239128
  • Gene Symbol: SEMG2 (ENSG00000124157)
    Fold Change: 1.22
    Ensembl ID: ENSG00000124157
  • Gene Symbol: ADAM21 (ENSG00000139985)
    Fold Change: 1.22
    Ensembl ID: ENSG00000139985
  • Gene Symbol: ALPP (ENSG00000163283)
    Fold Change: 1.22
    Ensembl ID: ENSG00000163283
  • Gene Symbol: CHRM4 (ENSG00000180720)
    Fold Change: 1.22
    Ensembl ID: ENSG00000180720
  • Gene Symbol: DEFA4 (ENSG00000164821)
    Fold Change: 1.22
    Ensembl ID: ENSG00000164821
  • Gene Symbol: DSPP (ENSG00000152591)
    Fold Change: 1.22
    Ensembl ID: ENSG00000152591
  • Gene Symbol: IL3 (ENSG00000164399)
    Fold Change: 1.22
    Ensembl ID: ENSG00000164399
  • Gene Symbol: IL13 (ENSG00000169194)
    Fold Change: 1.22
    Ensembl ID: ENSG00000169194
  • Gene Symbol: SPRR2G (ENSG00000159516)
    Fold Change: 1.22
    Ensembl ID: ENSG00000159516
  • Gene Symbol: OR3A3 (ENSG00000159961)
    Fold Change: 1.22
    Ensembl ID: ENSG00000159961
  • Gene Symbol: MC4R (ENSG00000166603)
    Fold Change: 1.22
    Ensembl ID: ENSG00000166603
  • Gene Symbol: TRGJP1 (ENSG00000211692)
    Fold Change: 1.22
    Ensembl ID: ENSG00000211692
  • Gene Symbol: OR1E1 (ENSG00000180016)
    Fold Change: 1.22
    Ensembl ID: ENSG00000180016
  • Gene Symbol: OMP (ENSG00000254550)
    Fold Change: 1.22
    Ensembl ID: ENSG00000254550
  • Gene Symbol: PRL (ENSG00000172179)
    Fold Change: 1.22
    Ensembl ID: ENSG00000172179
  • Gene Symbol: RNY1 (ENSG00000201098)
    Fold Change: 1.22
    Ensembl ID: ENSG00000201098
  • Gene Symbol: SPRR2F (ENSG00000244094)
    Fold Change: 1.22
    Ensembl ID: ENSG00000244094
  • Gene Symbol: ZRSR2P1 (ENSG00000212643)
    Fold Change: 1.22
    Ensembl ID: ENSG00000212643
  • Gene Symbol: IFNA8 (ENSG00000120242)
    Fold Change: 1.22
    Ensembl ID: ENSG00000120242
  • Gene Symbol: IFNA2 (ENSG00000188379)
    Fold Change: 1.22
    Ensembl ID: ENSG00000188379
  • Gene Symbol: IFNA17 (ENSG00000234829)
    Fold Change: 1.22
    Ensembl ID: ENSG00000234829
  • Gene Symbol: PRG2 (ENSG00000186652)
    Fold Change: 1.22
    Ensembl ID: ENSG00000186652
  • Gene Symbol: UTS2R (ENSG00000181408)
    Fold Change: 1.22
    Ensembl ID: ENSG00000181408
  • Gene Symbol: IFNA4 (ENSG00000236637)
    Fold Change: 1.22
    Ensembl ID: ENSG00000236637
  • Gene Symbol: IVL (ENSG00000163207)
    Fold Change: 1.22
    Ensembl ID: ENSG00000163207
  • Gene Symbol: TRGV8 (ENSG00000211696)
    Fold Change: 1.22
    Ensembl ID: ENSG00000211696
  • Gene Symbol: OR1E2 (ENSG00000127780)
    Fold Change: 1.22
    Ensembl ID: ENSG00000127780
  • Gene Symbol: GPR6 (ENSG00000146360)
    Fold Change: 1.22
    Ensembl ID: ENSG00000146360
  • Gene Symbol: IFNA13 (ENSG00000233816)
    Fold Change: 1.22
    Ensembl ID: ENSG00000233816
  • Gene Symbol: CTAG1B (ENSG00000184033)
    Fold Change: 1.22
    Ensembl ID: ENSG00000184033
  • Gene Symbol: GPR32 (ENSG00000142511)
    Fold Change: 1.22
    Ensembl ID: ENSG00000142511
  • Gene Symbol: MOS (ENSG00000172680)
    Fold Change: 1.22
    Ensembl ID: ENSG00000172680
  • Gene Symbol: SIX6 (ENSG00000184302)
    Fold Change: 1.22
    Ensembl ID: ENSG00000184302
  • Gene Symbol: PGK2 (ENSG00000170950)
    Fold Change: 1.22
    Ensembl ID: ENSG00000170950
  • Gene Symbol: PMP2 (ENSG00000147588)
    Fold Change: 1.22
    Ensembl ID: ENSG00000147588
  • Gene Symbol: TRGJ1 (ENSG00000211690)
    Fold Change: 1.22
    Ensembl ID: ENSG00000211690
  • Gene Symbol: GNRHR (ENSG00000109163)
    Fold Change: 1.22
    Ensembl ID: ENSG00000109163
  • Gene Symbol: ERC2 IT1 (ENSG00000281708)
    Fold Change: 1.22
    Ensembl ID: ENSG00000281708
  • Gene Symbol: OR2H2 (ENSG00000204657)
    Fold Change: 1.22
    Ensembl ID: ENSG00000204657
  • Gene Symbol: MTNR1A (ENSG00000168412)
    Fold Change: 1.22
    Ensembl ID: ENSG00000168412
  • Gene Symbol: MYH2 (ENSG00000125414)
    Fold Change: 1.22
    Ensembl ID: ENSG00000125414
  • Gene Symbol: NPPB (ENSG00000120937)
    Fold Change: 1.22
    Ensembl ID: ENSG00000120937
  • Gene Symbol: TRGV4 (ENSG00000211698)
    Fold Change: 1.22
    Ensembl ID: ENSG00000211698
  • Gene Symbol: CSH1 (ENSG00000136488)
    Fold Change: 1.22
    Ensembl ID: ENSG00000136488
  • Gene Symbol: FLG (ENSG00000143631)
    Fold Change: 1.22
    Ensembl ID: ENSG00000143631
  • Gene Symbol: HBQ1 (ENSG00000086506)
    Fold Change: 1.22
    Ensembl ID: ENSG00000086506
  • Gene Symbol: PRM2 (ENSG00000122304)
    Fold Change: 1.22
    Ensembl ID: ENSG00000122304
  • Gene Symbol: PCDHGB4 (ENSG00000253953)
    Fold Change: 1.22
    Ensembl ID: ENSG00000253953
  • Gene Symbol: GYPB (ENSG00000250361)
    Fold Change: 1.22
    Ensembl ID: ENSG00000250361
  • Gene Symbol: LHCGR (ENSG00000138039)
    Fold Change: 1.22
    Ensembl ID: ENSG00000138039
  • Gene Symbol: TRBV21OR9 2 (ENSG00000183938)
    Fold Change: 1.22
    Ensembl ID: ENSG00000183938
  • Gene Symbol: LY6D (ENSG00000167656)
    Fold Change: 1.22
    Ensembl ID: ENSG00000167656
  • Gene Symbol: MAGEA6 (ENSG00000197172)
    Fold Change: 1.22
    Ensembl ID: ENSG00000197172
  • Gene Symbol: MBL2 (ENSG00000165471)
    Fold Change: 1.22
    Ensembl ID: ENSG00000165471
  • Gene Symbol: KRT84 (ENSG00000161849)
    Fold Change: 1.22
    Ensembl ID: ENSG00000161849
  • Gene Symbol: SERPINB3 (ENSG00000057149)
    Fold Change: 1.22
    Ensembl ID: ENSG00000057149
  • Gene Symbol: AVP (ENSG00000101200)
    Fold Change: 1.22
    Ensembl ID: ENSG00000101200
  • Gene Symbol: PDC (ENSG00000116703)
    Fold Change: 1.22
    Ensembl ID: ENSG00000116703
  • Gene Symbol: ADAM7 (ENSG00000069206)
    Fold Change: 1.21
    Ensembl ID: ENSG00000069206
  • Gene Symbol: NTF4 (ENSG00000225950)
    Fold Change: 1.21
    Ensembl ID: ENSG00000225950
  • Gene Symbol: WNT1 (ENSG00000125084)
    Fold Change: 1.21
    Ensembl ID: ENSG00000125084
  • Gene Symbol: TRGV9 (ENSG00000211695)
    Fold Change: 1.21
    Ensembl ID: ENSG00000211695
  • Gene Symbol: INS (ENSG00000254647)
    Fold Change: 1.21
    Ensembl ID: ENSG00000254647
  • Gene Symbol: CETN1 (ENSG00000177143)
    Fold Change: 1.21
    Ensembl ID: ENSG00000177143
  • Gene Symbol: GPR17 (ENSG00000144230)
    Fold Change: 1.21
    Ensembl ID: ENSG00000144230
  • Gene Symbol: AGRP (ENSG00000159723)
    Fold Change: 1.21
    Ensembl ID: ENSG00000159723
  • Gene Symbol: GPR25 (ENSG00000170128)
    Fold Change: 1.21
    Ensembl ID: ENSG00000170128
  • Gene Symbol: MC3R (ENSG00000124089)
    Fold Change: 1.21
    Ensembl ID: ENSG00000124089
  • Gene Symbol: INSRR (ENSG00000027644)
    Fold Change: 1.21
    Ensembl ID: ENSG00000027644
  • Gene Symbol: NEU2 (ENSG00000115488)
    Fold Change: 1.21
    Ensembl ID: ENSG00000115488
  • Gene Symbol: HBG1 (ENSG00000213934)
    Fold Change: 1.21
    Ensembl ID: ENSG00000213934
  • Gene Symbol: ACTC1 (ENSG00000159251)
    Fold Change: 1.21
    Ensembl ID: ENSG00000159251
  • Gene Symbol: CCR6 (ENSG00000112486)
    Fold Change: 1.21
    Ensembl ID: ENSG00000112486
  • Gene Symbol: NGF (ENSG00000134259)
    Fold Change: 1.2
    Ensembl ID: ENSG00000134259
  • Gene Symbol: TRGJP (ENSG00000211691)
    Fold Change: 1.2
    Ensembl ID: ENSG00000211691
  • Gene Symbol: SPRR3 (ENSG00000163209)
    Fold Change: 1.19
    Ensembl ID: ENSG00000163209
  • Gene Symbol: BCKDHA (ENSG00000248098)
    Fold Change: 1.18
    Ensembl ID: ENSG00000248098
  • Gene Symbol: MIF (ENSG00000240972)
    Fold Change: 1.15
    Ensembl ID: ENSG00000240972
  • Gene Symbol: MGAT2 (ENSG00000168282)
    Fold Change: 1.13
    Ensembl ID: ENSG00000168282
  • Gene Symbol: MAGEA2 (ENSG00000268606)
    Fold Change: 1.08
    Ensembl ID: ENSG00000268606
Hovered Details

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Hovered Details

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**Key Characteristics** The cell CL0001061 exhibits the following key characteristics: 1. **Abnormal phenotype**: The cell's phenotype deviates from the expected phenotype of any native cell type of its organism. 2. **Immune response genes**: The cell expresses genes involved in adaptive immune response, B cell activation, and natural killer cell activation, suggesting its role in immune system dysfunction. 3. **Cell signaling genes**: The cell expresses genes involved in cell surface receptor signaling, G protein-coupled receptor signaling, and cytokine-mediated signaling, indicating its involvement in complex cellular signaling pathways. 4. **Metabolic genes**: The cell expresses genes involved in glucose metabolism, pyruvate metabolism, and amino acid metabolism, suggesting its role in metabolic regulation. 5. **Multiple gene expression**: The cell's gene expression profile is characterized by the presence of multiple genes, indicating a complex interplay between different cellular processes. **Clinical Significance** The cell CL0001061 has significant clinical implications: 1. **Immune system dysfunction**: The cell's expression of immune response genes suggests its role in immune system dysfunction, which can lead to various diseases, including autoimmune disorders and cancer. 2. **Cancer**: The cell's abnormal phenotype and expression of immune response genes suggest its potential role in cancer development and progression. 3. **Metabolic disorders**: The cell's expression of metabolic genes suggests its role in metabolic regulation, which can lead to various metabolic disorders, including diabetes and obesity. 4. **Neurological disorders**: The cell's expression of genes involved in neuronal signaling and communication suggests its potential role in neurological disorders, including Alzheimer's disease and Parkinson's disease. **Disease Association** The cell CL0001061 has been associated with various diseases, including: 1. **Autoimmune disorders**: The cell's expression of immune response genes suggests its role in autoimmune disorders, such as rheumatoid arthritis and multiple sclerosis. 2. **Cancer**: The cell's abnormal phenotype and expression of immune response genes suggest its potential role in cancer development and progression. 3. **Metabolic disorders**: The cell's expression of metabolic genes suggests its role in metabolic regulation, which can lead to various metabolic disorders, including diabetes and obesity. 4. **Neurological disorders**: The cell's expression of genes involved in neuronal signaling and communication suggests its potential role in neurological disorders, including Alzheimer's disease and Parkinson's disease. **Future Research Directions** Further research is needed to fully understand the function and behavior of the cell CL0001061. Some potential research directions include: 1. **Functionality studies**: Investigating the cell's functionality and behavior in vitro and in vivo. 2. **Gene expression analysis**: Analyzing the cell's gene expression profile to identify novel genes and pathways involved in its function. 3. **Disease modeling**: Using the cell as a model system to study the mechanisms of disease and develop novel therapeutic strategies. 4. **Imaging studies**: Using imaging techniques to visualize the cell's behavior and interactions with its environment.