Details for: PEX10
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: 93.5419
Cell Significance Index: -14.5500 - Cell Name: hematopoietic oligopotent progenitor cell (CL0002032)
Fold Change: 52.7907
Cell Significance Index: -13.3900 - Cell Name: embryonic stem cell (CL0002322)
Fold Change: 41.2674
Cell Significance Index: -17.0000 - Cell Name: smooth muscle fiber of ileum (CL1000278)
Fold Change: 32.8940
Cell Significance Index: -15.5300 - Cell Name: mucosal type mast cell (CL0000485)
Fold Change: 32.2456
Cell Significance Index: -13.1000 - Cell Name: ciliated cell of the bronchus (CL0002332)
Fold Change: 13.7524
Cell Significance Index: -13.1300 - Cell Name: orthochromatic erythroblast (CL0000552)
Fold Change: 12.4660
Cell Significance Index: -15.3700 - Cell Name: CD8-alpha-beta-positive, alpha-beta intraepithelial T cell (CL0000796)
Fold Change: 5.0320
Cell Significance Index: -13.4800 - Cell Name: stromal cell of bone marrow (CL0010001)
Fold Change: 3.9761
Cell Significance Index: -15.6900 - Cell Name: CD8-positive, alpha-beta regulatory T cell (CL0000795)
Fold Change: 3.1353
Cell Significance Index: -9.6300 - Cell Name: epidermal Langerhans cell (CL0002457)
Fold Change: 2.5359
Cell Significance Index: -5.5500 - Cell Name: conjunctival epithelial cell (CL1000432)
Fold Change: 1.1844
Cell Significance Index: 16.1600 - Cell Name: gut absorptive cell (CL0000677)
Fold Change: 1.0376
Cell Significance Index: 62.2900 - Cell Name: tuft cell of colon (CL0009041)
Fold Change: 1.0306
Cell Significance Index: 930.5300 - Cell Name: bladder urothelial cell (CL1001428)
Fold Change: 0.9383
Cell Significance Index: 48.7400 - Cell Name: cortical cell of adrenal gland (CL0002097)
Fold Change: 0.8811
Cell Significance Index: 23.6100 - Cell Name: colon goblet cell (CL0009039)
Fold Change: 0.7210
Cell Significance Index: 71.3200 - Cell Name: epithelial cell of small intestine (CL0002254)
Fold Change: 0.6804
Cell Significance Index: 110.6600 - Cell Name: intermediate cell of urothelium (CL4030055)
Fold Change: 0.4927
Cell Significance Index: 88.8300 - Cell Name: microfold cell of epithelium of small intestine (CL1000353)
Fold Change: 0.4862
Cell Significance Index: 33.6200 - Cell Name: acinar cell of salivary gland (CL0002623)
Fold Change: 0.4470
Cell Significance Index: 20.8400 - Cell Name: basal cell of urothelium (CL1000486)
Fold Change: 0.4190
Cell Significance Index: 51.5200 - Cell Name: neoplastic cell (CL0001063)
Fold Change: 0.3865
Cell Significance Index: 76.7000 - Cell Name: enteroendocrine cell of colon (CL0009042)
Fold Change: 0.3540
Cell Significance Index: 67.3700 - Cell Name: eye photoreceptor cell (CL0000287)
Fold Change: 0.3537
Cell Significance Index: 22.3000 - Cell Name: granulosa cell (CL0000501)
Fold Change: 0.3203
Cell Significance Index: 8.4200 - Cell Name: enterocyte of epithelium of large intestine (CL0002071)
Fold Change: 0.2606
Cell Significance Index: 11.8100 - Cell Name: cell in vitro (CL0001034)
Fold Change: 0.2490
Cell Significance Index: 136.0100 - Cell Name: odontoblast (CL0000060)
Fold Change: 0.2371
Cell Significance Index: 30.3900 - Cell Name: stromal cell of ovary (CL0002132)
Fold Change: 0.2335
Cell Significance Index: 32.0700 - Cell Name: enterocyte of epithelium of small intestine (CL1000334)
Fold Change: 0.2332
Cell Significance Index: 6.7200 - Cell Name: sebum secreting cell (CL0000317)
Fold Change: 0.2295
Cell Significance Index: 16.2300 - Cell Name: basal epithelial cell of tracheobronchial tree (CL0002329)
Fold Change: 0.2254
Cell Significance Index: 6.3000 - Cell Name: hair follicular keratinocyte (CL2000092)
Fold Change: 0.2231
Cell Significance Index: 98.6600 - Cell Name: kidney cell (CL1000497)
Fold Change: 0.2167
Cell Significance Index: 1.7300 - Cell Name: mesonephric nephron tubule epithelial cell (CL1000022)
Fold Change: 0.2135
Cell Significance Index: 7.4200 - Cell Name: umbrella cell of urothelium (CL4030056)
Fold Change: 0.2020
Cell Significance Index: 1.8600 - Cell Name: fibroblast of dermis (CL0002551)
Fold Change: 0.1918
Cell Significance Index: 4.0200 - Cell Name: lactocyte (CL0002325)
Fold Change: 0.1877
Cell Significance Index: 24.2500 - Cell Name: basal cell of prostate epithelium (CL0002341)
Fold Change: 0.1773
Cell Significance Index: 4.8300 - Cell Name: progenitor cell of mammary luminal epithelium (CL0009116)
Fold Change: 0.1623
Cell Significance Index: 12.1000 - Cell Name: L2/3-6 intratelencephalic projecting glutamatergic neuron (CL4023040)
Fold Change: 0.1580
Cell Significance Index: 31.6900 - Cell Name: GABAergic interneuron (CL0011005)
Fold Change: 0.1196
Cell Significance Index: 82.7200 - Cell Name: early pro-B cell (CL0002046)
Fold Change: 0.0973
Cell Significance Index: 6.2800 - Cell Name: skeletal muscle myoblast (CL0000515)
Fold Change: 0.0957
Cell Significance Index: 1.0400 - Cell Name: obsolete caudal ganglionic eminence derived GABAergic cortical interneuron (CL4023070)
Fold Change: 0.0781
Cell Significance Index: 28.0200 - Cell Name: intestinal crypt stem cell of small intestine (CL0009017)
Fold Change: 0.0664
Cell Significance Index: 1.4200 - Cell Name: luminal adaptive secretory precursor cell of mammary gland (CL4033057)
Fold Change: 0.0643
Cell Significance Index: 3.0200 - Cell Name: tonsil germinal center B cell (CL2000006)
Fold Change: 0.0562
Cell Significance Index: 6.6300 - Cell Name: pancreatic acinar cell (CL0002064)
Fold Change: 0.0346
Cell Significance Index: 5.9000 - Cell Name: glycinergic neuron (CL1001509)
Fold Change: 0.0337
Cell Significance Index: 1.7700 - Cell Name: cardiac muscle myoblast (CL0000513)
Fold Change: 0.0334
Cell Significance Index: 2.5700 - Cell Name: retinal progenitor cell (CL0002672)
Fold Change: 0.0182
Cell Significance Index: 1.0200 - Cell Name: pigmented epithelial cell (CL0000529)
Fold Change: 0.0090
Cell Significance Index: 16.8700 - Cell Name: placental villous trophoblast (CL2000060)
Fold Change: 0.0060
Cell Significance Index: 0.1600 - Cell Name: transit amplifying cell of colon (CL0009011)
Fold Change: 0.0028
Cell Significance Index: 0.0900 - Cell Name: lens epithelial cell (CL0002224)
Fold Change: 0.0015
Cell Significance Index: 2.3700 - Cell Name: anterior lens cell (CL0002223)
Fold Change: 0.0006
Cell Significance Index: 1.1600 - Cell Name: kidney loop of Henle cortical thick ascending limb epithelial cell (CL1001109)
Fold Change: -0.0011
Cell Significance Index: -0.7900 - Cell Name: transit amplifying cell of small intestine (CL0009012)
Fold Change: -0.0014
Cell Significance Index: -0.0300 - Cell Name: secondary lens fiber (CL0002225)
Fold Change: -0.0048
Cell Significance Index: -6.5500 - Cell Name: pulmonary alveolar epithelial cell (CL0000322)
Fold Change: -0.0058
Cell Significance Index: -4.4200 - Cell Name: forebrain neuroblast (CL1000042)
Fold Change: -0.0109
Cell Significance Index: -0.6700 - Cell Name: non-pigmented ciliary epithelial cell (CL0002304)
Fold Change: -0.0118
Cell Significance Index: -7.4900 - Cell Name: mesenchymal cell (CL0008019)
Fold Change: -0.0152
Cell Significance Index: -0.2600 - Cell Name: abnormal cell (CL0001061)
Fold Change: -0.0167
Cell Significance Index: -1.7100 - Cell Name: pancreatic A cell (CL0000171)
Fold Change: -0.0181
Cell Significance Index: -13.4200 - Cell Name: ciliary muscle cell (CL1000443)
Fold Change: -0.0238
Cell Significance Index: -10.7800 - Cell Name: type B pancreatic cell (CL0000169)
Fold Change: -0.0246
Cell Significance Index: -13.8700 - Cell Name: pancreatic PP cell (CL0002275)
Fold Change: -0.0296
Cell Significance Index: -18.4700 - Cell Name: pigmented ciliary epithelial cell (CL0002303)
Fold Change: -0.0394
Cell Significance Index: -5.7300 - Cell Name: dopaminergic neuron (CL0000700)
Fold Change: -0.0409
Cell Significance Index: -11.7700 - Cell Name: epithelial cell of stomach (CL0002178)
Fold Change: -0.0512
Cell Significance Index: -5.9700 - Cell Name: retinal rod cell (CL0000604)
Fold Change: -0.0554
Cell Significance Index: -0.6600 - Cell Name: pro-T cell (CL0000827)
Fold Change: -0.0712
Cell Significance Index: -1.8200 - Cell Name: pancreatic ductal cell (CL0002079)
Fold Change: -0.0715
Cell Significance Index: -8.1900 - Cell Name: enteroendocrine cell of small intestine (CL0009006)
Fold Change: -0.0868
Cell Significance Index: -2.1700 - Cell Name: pancreatic D cell (CL0000173)
Fold Change: -0.0875
Cell Significance Index: -18.4300 - Cell Name: kidney loop of Henle descending limb epithelial cell (CL1001021)
Fold Change: -0.1331
Cell Significance Index: -10.5500 - Cell Name: smooth muscle cell of sphincter of pupil (CL0002243)
Fold Change: -0.1370
Cell Significance Index: -14.2700 - Cell Name: endothelial cell of venule (CL1000414)
Fold Change: -0.1479
Cell Significance Index: -1.6800 - Cell Name: hippocampal granule cell (CL0001033)
Fold Change: -0.1502
Cell Significance Index: -10.1000 - Cell Name: CD4-positive, alpha-beta memory T cell, CD45RO-positive (CL0001204)
Fold Change: -0.1590
Cell Significance Index: -4.6700 - Cell Name: paneth cell of epithelium of small intestine (CL1000343)
Fold Change: -0.1648
Cell Significance Index: -3.5700 - Cell Name: interstitial cell of ovary (CL0002094)
Fold Change: -0.1773
Cell Significance Index: -2.2700 - Cell Name: lung endothelial cell (CL1001567)
Fold Change: -0.1830
Cell Significance Index: -9.5300 - Cell Name: neutrophil progenitor cell (CL0000834)
Fold Change: -0.1892
Cell Significance Index: -5.0600 - Cell Name: kidney epithelial cell (CL0002518)
Fold Change: -0.2023
Cell Significance Index: -5.9600 - Cell Name: indirect pathway medium spiny neuron (CL4023029)
Fold Change: -0.2112
Cell Significance Index: -9.3400 - Cell Name: intestinal tuft cell (CL0019032)
Fold Change: -0.2160
Cell Significance Index: -13.2400 - Cell Name: peg cell (CL4033014)
Fold Change: -0.2164
Cell Significance Index: -5.0000 - Cell Name: direct pathway medium spiny neuron (CL4023026)
Fold Change: -0.2377
Cell Significance Index: -9.0000 - Cell Name: intestinal epithelial cell (CL0002563)
Fold Change: -0.2386
Cell Significance Index: -2.4700 - Cell Name: keratocyte (CL0002363)
Fold Change: -0.2389
Cell Significance Index: -3.7900 - Cell Name: radial glial cell (CL0000681)
Fold Change: -0.2553
Cell Significance Index: -1.5200 - Cell Name: medial ganglionic eminence derived interneuron (CL4023063)
Fold Change: -0.2687
Cell Significance Index: -3.8500 - Cell Name: Purkinje cell (CL0000121)
Fold Change: -0.2827
Cell Significance Index: -6.1900 - Cell Name: microcirculation associated smooth muscle cell (CL0008035)
Fold Change: -0.2952
Cell Significance Index: -2.4800 - Cell Name: glioblast (CL0000030)
Fold Change: -0.2994
Cell Significance Index: -1.8800 - Cell Name: skeletal muscle fiber (CL0008002)
Fold Change: -0.3163
Cell Significance Index: -8.1300
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.
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.
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
Genular Protein ID: 2612234687
Symbol: PEX10_HUMAN
Name: Peroxisomal biogenesis factor 10
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 9683594
Title: Identification of PEX10, the gene defective in complementation group 7 of the peroxisome-biogenesis disorders.
PubMed ID: 9683594
DOI: 10.1086/301963
PubMed ID: 9700193
Title: Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group B.
PubMed ID: 9700193
DOI: 10.1093/hmg/7.9.1399
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
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: 9922452
Title: Peroxisome synthesis in the absence of preexisting peroxisomes.
PubMed ID: 9922452
PubMed ID: 10704444
Title: PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis.
PubMed ID: 10704444
PubMed ID: 11390669
Title: Human pex19p binds peroxisomal integral membrane proteins at regions distinct from their sorting sequences.
PubMed ID: 11390669
PubMed ID: 24662292
Title: Distinct modes of ubiquitination of peroxisome-targeting signal type 1 (PTS1) receptor Pex5p regulate PTS1 protein import.
PubMed ID: 24662292
PubMed ID: 30022445
Title: PEX10-related autosomal recessive cerebellar ataxia with hearing loss.
PubMed ID: 30022445
PubMed ID: 17041890
Title: Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.
PubMed ID: 17041890
DOI: 10.1002/humu.9462
PubMed ID: 19105186
Title: Identification of novel mutations and sequence variation in the Zellweger syndrome spectrum of peroxisome biogenesis disorders.
PubMed ID: 19105186
DOI: 10.1002/humu.20932
PubMed ID: 20695019
Title: Mutations in PEX10 are a cause of autosomal recessive ataxia.
PubMed ID: 20695019
DOI: 10.1002/ana.22035
PubMed ID: 27230853
Title: Expanding the spectrum of PEX10-related peroxisomal biogenesis disorders: slowly progressive recessive ataxia.
PubMed ID: 27230853
PubMed ID: 28784167
Title: Identification of a novel mutation in PEX10 in a patient with attenuated Zellweger spectrum disorder: a case report.
PubMed ID: 28784167
PubMed ID: 32069232
Title: Two different missense mutations of PEX genes in two similar patients with severe Zellweger syndrome: an argument on the genotype-phenotype correlation.
PubMed ID: 32069232
Sequence Information:
- Length: 326
- Mass: 37069
- Checksum: 9CF2CE5E4C797799
- Sequence:
MAPAAASPPE VIRAAQKDEY YRGGLRSAAG GALHSLAGAR KWLEWRKEVE LLSDVAYFGL TTLAGYQTLG EEYVSIIQVD PSRIHVPSSL RRGVLVTLHA VLPYLLDKAL LPLEQELQAD PDSGRPLQGS LGPGGRGCSG ARRWMRHHTA TLTEQQRRAL LRAVFVLRQG LACLQRLHVA WFYIHGVFYH LAKRLTGITY LRVRSLPGED LRARVSYRLL GVISLLHLVL SMGLQLYGFR QRQRARKEWR LHRGLSHRRA SLEERAVSRN PLCTLCLEER RHPTATPCGH LFCWECITAW CSSKAECPLC REKFPPQKLI YLRHYR
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.