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Gene: DNAJC8 |
Gene summary for DNAJC8 |
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Gene information | Species | Human | Gene symbol | DNAJC8 | Gene ID | 22826 |
Gene name | DnaJ heat shock protein family (Hsp40) member C8 | |
Gene Alias | HSPC331 | |
Cytomap | 1p35.3 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | O75937 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
22826 | DNAJC8 | P65T-E | Human | Esophagus | ESCC | 1.14e-37 | 7.59e-01 | 0.0978 |
22826 | DNAJC8 | P74T-E | Human | Esophagus | ESCC | 6.42e-59 | 2.02e+00 | 0.1479 |
22826 | DNAJC8 | P75T-E | Human | Esophagus | ESCC | 2.61e-70 | 1.64e+00 | 0.1125 |
22826 | DNAJC8 | P76T-E | Human | Esophagus | ESCC | 1.10e-48 | 9.75e-01 | 0.1207 |
22826 | DNAJC8 | P79T-E | Human | Esophagus | ESCC | 5.23e-52 | 1.10e+00 | 0.1154 |
22826 | DNAJC8 | P80T-E | Human | Esophagus | ESCC | 2.21e-54 | 1.67e+00 | 0.155 |
22826 | DNAJC8 | P82T-E | Human | Esophagus | ESCC | 6.41e-26 | 1.36e+00 | 0.1072 |
22826 | DNAJC8 | P83T-E | Human | Esophagus | ESCC | 7.12e-58 | 1.62e+00 | 0.1738 |
22826 | DNAJC8 | P84T-E | Human | Esophagus | ESCC | 4.66e-08 | 6.46e-01 | 0.0933 |
22826 | DNAJC8 | P89T-E | Human | Esophagus | ESCC | 1.54e-16 | 1.35e+00 | 0.1752 |
22826 | DNAJC8 | P91T-E | Human | Esophagus | ESCC | 1.12e-18 | 2.57e+00 | 0.1828 |
22826 | DNAJC8 | P104T-E | Human | Esophagus | ESCC | 1.92e-03 | 7.76e-01 | 0.0931 |
22826 | DNAJC8 | P107T-E | Human | Esophagus | ESCC | 9.24e-79 | 1.54e+00 | 0.171 |
22826 | DNAJC8 | P126T-E | Human | Esophagus | ESCC | 3.28e-16 | 1.18e+00 | 0.1125 |
22826 | DNAJC8 | P127T-E | Human | Esophagus | ESCC | 4.41e-34 | 6.32e-01 | 0.0826 |
22826 | DNAJC8 | P128T-E | Human | Esophagus | ESCC | 2.57e-53 | 1.69e+00 | 0.1241 |
22826 | DNAJC8 | P130T-E | Human | Esophagus | ESCC | 1.97e-99 | 2.15e+00 | 0.1676 |
22826 | DNAJC8 | S43 | Human | Liver | Cirrhotic | 6.53e-10 | -3.57e-01 | -0.0187 |
22826 | DNAJC8 | HCC1_Meng | Human | Liver | HCC | 1.83e-93 | -6.64e-04 | 0.0246 |
22826 | DNAJC8 | HCC2_Meng | Human | Liver | HCC | 7.76e-32 | -1.75e-01 | 0.0107 |
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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 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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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 |
DNAJC8 | insertion | In_Frame_Ins | novel | c.23_24insAGTTTTGCTCTTGTTGCCCAGGCCTGGAGTGCA | p.Gly8_Thr9insValLeuLeuLeuLeuProArgProGlyValGln | p.G8_T9insVLLLLPRPGVQ | O75937 | protein_coding | TCGA-B6-A0I6-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | PD | ||
DNAJC8 | SNV | Missense_Mutation | c.126N>C | p.Gln42His | p.Q42H | O75937 | protein_coding | deleterious(0.02) | benign(0.183) | TCGA-C5-A1BK-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
DNAJC8 | SNV | Missense_Mutation | c.583N>A | p.Glu195Lys | p.E195K | O75937 | protein_coding | tolerated(0.05) | possibly_damaging(0.614) | TCGA-C5-A1BQ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Chemotherapy | cisplatin | CR | |
DNAJC8 | SNV | Missense_Mutation | c.583N>A | p.Glu195Lys | p.E195K | O75937 | protein_coding | tolerated(0.05) | possibly_damaging(0.614) | TCGA-C5-A3HL-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
DNAJC8 | SNV | Missense_Mutation | novel | c.76N>A | p.Glu26Lys | p.E26K | O75937 | protein_coding | deleterious(0) | probably_damaging(0.983) | TCGA-MA-AA41-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
DNAJC8 | insertion | In_Frame_Ins | novel | c.655_656insTAT | p.Arg219delinsLeuCys | p.R219delinsLC | O75937 | protein_coding | TCGA-DS-A1OC-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | gemcitabine | SD | ||
DNAJC8 | SNV | Missense_Mutation | c.643N>C | p.Ser215Arg | p.S215R | O75937 | protein_coding | deleterious(0) | possibly_damaging(0.526) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
DNAJC8 | SNV | Missense_Mutation | novel | c.263N>C | p.Lys88Thr | p.K88T | O75937 | protein_coding | deleterious(0.02) | probably_damaging(0.987) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
DNAJC8 | SNV | Missense_Mutation | c.20G>A | p.Ser7Asn | p.S7N | O75937 | protein_coding | tolerated(0.17) | benign(0.015) | TCGA-G4-6304-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Chemotherapy | fluorouracil | PD | |
DNAJC8 | SNV | Missense_Mutation | c.228N>C | p.Arg76Ser | p.R76S | O75937 | protein_coding | deleterious(0.01) | benign(0.324) | TCGA-NH-A5IV-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | 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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