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Gene: CLN5 |
Gene summary for CLN5 |
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Gene information | Species | Human | Gene symbol | CLN5 | Gene ID | 1203 |
Gene name | CLN5 intracellular trafficking protein | |
Gene Alias | CLN5 | |
Cytomap | 13q22.3 | |
Gene Type | protein-coding | GO ID | GO:0006465 | UniProtAcc | A0A024R644 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
1203 | CLN5 | LZE4T | Human | Esophagus | ESCC | 1.16e-07 | 1.30e-01 | 0.0811 |
1203 | CLN5 | LZE5T | Human | Esophagus | ESCC | 2.67e-02 | 2.73e-01 | 0.0514 |
1203 | CLN5 | LZE7T | Human | Esophagus | ESCC | 3.10e-03 | 2.03e-01 | 0.0667 |
1203 | CLN5 | LZE8T | Human | Esophagus | ESCC | 1.95e-05 | 1.15e-01 | 0.067 |
1203 | CLN5 | LZE20T | Human | Esophagus | ESCC | 4.34e-07 | 1.34e-01 | 0.0662 |
1203 | CLN5 | LZE24T | Human | Esophagus | ESCC | 6.50e-08 | 2.03e-01 | 0.0596 |
1203 | CLN5 | P1T-E | Human | Esophagus | ESCC | 2.06e-04 | 2.32e-01 | 0.0875 |
1203 | CLN5 | P2T-E | Human | Esophagus | ESCC | 7.60e-18 | 2.42e-01 | 0.1177 |
1203 | CLN5 | P4T-E | Human | Esophagus | ESCC | 1.08e-19 | 3.46e-01 | 0.1323 |
1203 | CLN5 | P5T-E | Human | Esophagus | ESCC | 6.89e-06 | 9.61e-02 | 0.1327 |
1203 | CLN5 | P8T-E | Human | Esophagus | ESCC | 2.17e-24 | 4.96e-01 | 0.0889 |
1203 | CLN5 | P9T-E | Human | Esophagus | ESCC | 1.20e-19 | 4.74e-01 | 0.1131 |
1203 | CLN5 | P10T-E | Human | Esophagus | ESCC | 7.48e-35 | 5.83e-01 | 0.116 |
1203 | CLN5 | P11T-E | Human | Esophagus | ESCC | 2.95e-18 | 7.44e-01 | 0.1426 |
1203 | CLN5 | P12T-E | Human | Esophagus | ESCC | 5.92e-13 | 2.65e-01 | 0.1122 |
1203 | CLN5 | P15T-E | Human | Esophagus | ESCC | 6.60e-09 | 2.37e-01 | 0.1149 |
1203 | CLN5 | P16T-E | Human | Esophagus | ESCC | 3.39e-23 | 4.06e-01 | 0.1153 |
1203 | CLN5 | P19T-E | Human | Esophagus | ESCC | 4.62e-11 | 6.34e-01 | 0.1662 |
1203 | CLN5 | P20T-E | Human | Esophagus | ESCC | 3.97e-12 | 3.11e-01 | 0.1124 |
1203 | CLN5 | P21T-E | Human | Esophagus | ESCC | 9.15e-18 | 2.49e-01 | 0.1617 |
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∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
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Malignant transformation related pathway analysis |
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Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | ![]() |
Colorectum | SER | ![]() |
Colorectum | MSS | ![]() |
Colorectum | MSI-H | ![]() |
Colorectum | FAP | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:005160420 | Thyroid | PTC | protein maturation | 132/5968 | 294/18723 | 1.71e-06 | 2.39e-05 | 132 |
GO:00421479 | Thyroid | PTC | retrograde transport, endosome to Golgi | 48/5968 | 91/18723 | 2.86e-05 | 2.78e-04 | 48 |
GO:00070405 | Thyroid | PTC | lysosome organization | 38/5968 | 74/18723 | 3.84e-04 | 2.58e-03 | 38 |
GO:00801715 | Thyroid | PTC | lytic vacuole organization | 38/5968 | 74/18723 | 3.84e-04 | 2.58e-03 | 38 |
GO:000646519 | Thyroid | PTC | signal peptide processing | 11/5968 | 14/18723 | 4.45e-04 | 2.95e-03 | 11 |
GO:00164859 | Thyroid | PTC | protein processing | 95/5968 | 225/18723 | 6.60e-04 | 4.15e-03 | 95 |
GO:1904424 | Thyroid | PTC | regulation of GTP binding | 11/5968 | 15/18723 | 1.19e-03 | 6.84e-03 | 11 |
GO:00070355 | Thyroid | PTC | vacuolar acidification | 15/5968 | 24/18723 | 1.95e-03 | 1.05e-02 | 15 |
GO:00700855 | Thyroid | PTC | glycosylation | 96/5968 | 240/18723 | 4.57e-03 | 2.15e-02 | 96 |
GO:005109834 | Thyroid | ATC | regulation of binding | 203/6293 | 363/18723 | 1.18e-18 | 1.55e-16 | 203 |
GO:005109934 | Thyroid | ATC | positive regulation of binding | 103/6293 | 173/18723 | 2.19e-12 | 9.05e-11 | 103 |
GO:001619719 | Thyroid | ATC | endosomal transport | 128/6293 | 230/18723 | 4.44e-12 | 1.75e-10 | 128 |
GO:000703322 | Thyroid | ATC | vacuole organization | 100/6293 | 180/18723 | 1.07e-09 | 2.71e-08 | 100 |
GO:001648218 | Thyroid | ATC | cytosolic transport | 93/6293 | 168/18723 | 5.19e-09 | 1.15e-07 | 93 |
GO:0051604110 | Thyroid | ATC | protein maturation | 136/6293 | 294/18723 | 4.00e-06 | 4.42e-05 | 136 |
GO:004214715 | Thyroid | ATC | retrograde transport, endosome to Golgi | 49/6293 | 91/18723 | 5.48e-05 | 4.23e-04 | 49 |
GO:001648515 | Thyroid | ATC | protein processing | 100/6293 | 225/18723 | 4.39e-04 | 2.62e-03 | 100 |
GO:000704012 | Thyroid | ATC | lysosome organization | 39/6293 | 74/18723 | 5.41e-04 | 3.13e-03 | 39 |
GO:008017112 | Thyroid | ATC | lytic vacuole organization | 39/6293 | 74/18723 | 5.41e-04 | 3.13e-03 | 39 |
GO:000646521 | Thyroid | ATC | signal peptide processing | 11/6293 | 14/18723 | 7.46e-04 | 4.14e-03 | 11 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0414222 | Esophagus | ESCC | Lysosome | 102/4205 | 132/8465 | 5.11e-11 | 7.13e-10 | 3.65e-10 | 102 |
hsa0414232 | Esophagus | ESCC | Lysosome | 102/4205 | 132/8465 | 5.11e-11 | 7.13e-10 | 3.65e-10 | 102 |
hsa041425 | Oral cavity | OSCC | Lysosome | 87/3704 | 132/8465 | 1.97e-07 | 1.35e-06 | 6.86e-07 | 87 |
hsa0414212 | Oral cavity | OSCC | Lysosome | 87/3704 | 132/8465 | 1.97e-07 | 1.35e-06 | 6.86e-07 | 87 |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
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Somatic mutation of malignant transformation related genes |
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Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
CLN5 | SNV | Missense_Mutation | c.832N>C | p.Tyr278His | p.Y278H | protein_coding | deleterious(0.04) | probably_damaging(0.97) | TCGA-A8-A06Q-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | ||
CLN5 | SNV | Missense_Mutation | c.757G>C | p.Glu253Gln | p.E253Q | protein_coding | tolerated(0.15) | probably_damaging(0.939) | TCGA-LP-A5U2-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unknown | Unknown | SD | ||
CLN5 | SNV | Missense_Mutation | c.1126N>G | p.Phe376Val | p.F376V | protein_coding | tolerated(0.23) | possibly_damaging(0.511) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | ||
CLN5 | SNV | Missense_Mutation | novel | c.1081N>G | p.Phe361Val | p.F361V | protein_coding | tolerated(0.16) | possibly_damaging(0.591) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
CLN5 | SNV | Missense_Mutation | c.596G>A | p.Arg199Gln | p.R199Q | protein_coding | tolerated(0.12) | probably_damaging(0.997) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | ||
CLN5 | SNV | Missense_Mutation | rs770688728 | c.1016G>T | p.Arg339Ile | p.R339I | protein_coding | deleterious(0.03) | benign(0.419) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
CLN5 | SNV | Missense_Mutation | c.322N>T | p.Arg108Cys | p.R108C | protein_coding | deleterious_low_confidence(0) | probably_damaging(0.999) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
CLN5 | SNV | Missense_Mutation | novel | c.1160T>G | p.Phe387Cys | p.F387C | protein_coding | deleterious(0.01) | probably_damaging(0.976) | TCGA-AP-A1E0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | SD | |
CLN5 | SNV | Missense_Mutation | novel | c.758N>T | p.Glu253Val | p.E253V | protein_coding | deleterious(0.02) | probably_damaging(0.974) | TCGA-AX-A06F-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | SD | |
CLN5 | SNV | Missense_Mutation | novel | c.448N>A | p.Val150Ile | p.V150I | protein_coding | tolerated(0.13) | benign(0.175) | TCGA-AX-A1C5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unspecific | Carboplatin | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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