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Gene: CAPN13 |
Gene summary for CAPN13 |
Gene summary. |
Gene information | Species | Human | Gene symbol | CAPN13 | Gene ID | 92291 |
Gene name | calpain 13 | |
Gene Alias | CAPN13 | |
Cytomap | 2p23.1 | |
Gene Type | protein-coding | GO ID | GO:0006508 | UniProtAcc | Q6MZZ7 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
92291 | CAPN13 | LZE5T | Human | Esophagus | ESCC | 1.54e-04 | 4.90e-01 | 0.0514 |
92291 | CAPN13 | LZE24T | Human | Esophagus | ESCC | 1.89e-10 | 2.66e-01 | 0.0596 |
92291 | CAPN13 | P1T-E | Human | Esophagus | ESCC | 1.09e-04 | 2.22e-01 | 0.0875 |
92291 | CAPN13 | P8T-E | Human | Esophagus | ESCC | 3.02e-26 | 6.95e-01 | 0.0889 |
92291 | CAPN13 | P15T-E | Human | Esophagus | ESCC | 3.38e-04 | 2.52e-01 | 0.1149 |
92291 | CAPN13 | P23T-E | Human | Esophagus | ESCC | 6.53e-09 | 2.49e-01 | 0.108 |
92291 | CAPN13 | P36T-E | Human | Esophagus | ESCC | 2.82e-02 | 1.59e-01 | 0.1187 |
92291 | CAPN13 | P57T-E | Human | Esophagus | ESCC | 9.35e-10 | 3.11e-01 | 0.0926 |
92291 | CAPN13 | P61T-E | Human | Esophagus | ESCC | 2.11e-11 | 3.17e-01 | 0.099 |
92291 | CAPN13 | P62T-E | Human | Esophagus | ESCC | 8.96e-66 | 1.81e+00 | 0.1302 |
92291 | CAPN13 | P65T-E | Human | Esophagus | ESCC | 2.64e-10 | 2.41e-01 | 0.0978 |
92291 | CAPN13 | P76T-E | Human | Esophagus | ESCC | 3.75e-03 | 1.67e-01 | 0.1207 |
92291 | CAPN13 | P79T-E | Human | Esophagus | ESCC | 2.06e-08 | 2.84e-01 | 0.1154 |
92291 | CAPN13 | P80T-E | Human | Esophagus | ESCC | 1.97e-04 | 2.82e-01 | 0.155 |
92291 | CAPN13 | P82T-E | Human | Esophagus | ESCC | 1.40e-05 | 3.53e-01 | 0.1072 |
92291 | CAPN13 | P84T-E | Human | Esophagus | ESCC | 2.04e-06 | 4.93e-01 | 0.0933 |
92291 | CAPN13 | P104T-E | Human | Esophagus | ESCC | 2.06e-06 | 3.35e-01 | 0.0931 |
92291 | CAPN13 | P126T-E | Human | Esophagus | ESCC | 8.75e-03 | 5.07e-01 | 0.1125 |
92291 | CAPN13 | P127T-E | Human | Esophagus | ESCC | 7.67e-11 | 2.40e-01 | 0.0826 |
92291 | CAPN13 | RNA-P17T-P17T-2 | Human | Lung | IAC | 2.46e-03 | 5.95e-01 | 0.3371 |
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Transcriptomic changes along malignancy continuum. |
∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
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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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
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 |
Annotation of somatic variants for genes involved in malignant transformation |
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 |
CAPN13 | SNV | Missense_Mutation | c.631N>A | p.Asp211Asn | p.D211N | Q6MZZ7 | protein_coding | tolerated(0.32) | benign(0.174) | TCGA-A2-A0D2-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | |
CAPN13 | SNV | Missense_Mutation | novel | c.1244N>T | p.Ser415Leu | p.S415L | Q6MZZ7 | protein_coding | tolerated(0.65) | benign(0.062) | TCGA-MS-A51U-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD |
CAPN13 | insertion | In_Frame_Ins | novel | c.1682_1683insAAATGTAAAATCACATTTCCCCGG | p.Glu561_Glu562insAsnValLysSerHisPheProGly | p.E561_E562insNVKSHFPG | Q6MZZ7 | protein_coding | TCGA-A2-A04Y-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | ||
CAPN13 | insertion | Nonsense_Mutation | novel | c.1526_1527insA | p.Tyr509Ter | p.Y509* | Q6MZZ7 | protein_coding | TCGA-A2-A0YH-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | SD | ||
CAPN13 | insertion | Nonsense_Mutation | novel | c.453_454insGTCCGATGAGAGTGCGGAGGAG | p.Cys152ValfsTer3 | p.C152Vfs*3 | Q6MZZ7 | protein_coding | TCGA-AN-A0G0-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
CAPN13 | insertion | Nonsense_Mutation | novel | c.451_452insTTTAATAATATCACGGTCA | p.Lys151IlefsTer2 | p.K151Ifs*2 | Q6MZZ7 | protein_coding | TCGA-AN-A0G0-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
CAPN13 | SNV | Missense_Mutation | novel | c.1383G>T | p.Gln461His | p.Q461H | Q6MZZ7 | protein_coding | tolerated(0.09) | possibly_damaging(0.652) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
CAPN13 | SNV | Missense_Mutation | rs201284844 | c.5N>T | p.Ala2Val | p.A2V | Q6MZZ7 | protein_coding | deleterious(0) | possibly_damaging(0.893) | TCGA-EA-A410-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
CAPN13 | SNV | Missense_Mutation | c.955N>C | p.Asp319His | p.D319H | Q6MZZ7 | protein_coding | deleterious(0.01) | probably_damaging(0.997) | TCGA-IR-A3LK-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD | |
CAPN13 | SNV | Missense_Mutation | c.788N>A | p.Arg263Lys | p.R263K | Q6MZZ7 | protein_coding | tolerated(0.59) | benign(0.035) | TCGA-UC-A7PF-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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