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Gene: CIAPIN1 |
Gene summary for CIAPIN1 |
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Gene information | Species | Human | Gene symbol | CIAPIN1 | Gene ID | 57019 |
Gene name | cytokine induced apoptosis inhibitor 1 | |
Gene Alias | Anamorsin | |
Cytomap | 16q21 | |
Gene Type | protein-coding | GO ID | GO:0002376 | UniProtAcc | Q6FI81 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
57019 | CIAPIN1 | LZE4T | Human | Esophagus | ESCC | 1.11e-17 | 5.32e-01 | 0.0811 |
57019 | CIAPIN1 | LZE5T | Human | Esophagus | ESCC | 1.88e-02 | 2.27e-01 | 0.0514 |
57019 | CIAPIN1 | LZE7T | Human | Esophagus | ESCC | 3.25e-10 | 5.80e-01 | 0.0667 |
57019 | CIAPIN1 | LZE8T | Human | Esophagus | ESCC | 4.11e-08 | 3.14e-01 | 0.067 |
57019 | CIAPIN1 | LZE20T | Human | Esophagus | ESCC | 5.81e-05 | 1.98e-01 | 0.0662 |
57019 | CIAPIN1 | LZE22D1 | Human | Esophagus | HGIN | 4.60e-03 | 1.48e-01 | 0.0595 |
57019 | CIAPIN1 | LZE22T | Human | Esophagus | ESCC | 3.92e-05 | 4.38e-01 | 0.068 |
57019 | CIAPIN1 | LZE24T | Human | Esophagus | ESCC | 2.46e-19 | 4.81e-01 | 0.0596 |
57019 | CIAPIN1 | LZE6T | Human | Esophagus | ESCC | 2.84e-03 | 1.83e-01 | 0.0845 |
57019 | CIAPIN1 | P1T-E | Human | Esophagus | ESCC | 4.18e-09 | 4.88e-01 | 0.0875 |
57019 | CIAPIN1 | P2T-E | Human | Esophagus | ESCC | 1.39e-22 | 3.97e-01 | 0.1177 |
57019 | CIAPIN1 | P4T-E | Human | Esophagus | ESCC | 2.05e-39 | 7.59e-01 | 0.1323 |
57019 | CIAPIN1 | P5T-E | Human | Esophagus | ESCC | 3.23e-26 | 5.31e-01 | 0.1327 |
57019 | CIAPIN1 | P8T-E | Human | Esophagus | ESCC | 4.08e-25 | 4.36e-01 | 0.0889 |
57019 | CIAPIN1 | P9T-E | Human | Esophagus | ESCC | 6.15e-13 | 3.38e-01 | 0.1131 |
57019 | CIAPIN1 | P10T-E | Human | Esophagus | ESCC | 3.75e-30 | 4.29e-01 | 0.116 |
57019 | CIAPIN1 | P11T-E | Human | Esophagus | ESCC | 4.26e-15 | 5.09e-01 | 0.1426 |
57019 | CIAPIN1 | P12T-E | Human | Esophagus | ESCC | 3.43e-24 | 4.52e-01 | 0.1122 |
57019 | CIAPIN1 | P15T-E | Human | Esophagus | ESCC | 1.72e-21 | 4.91e-01 | 0.1149 |
57019 | CIAPIN1 | P16T-E | Human | Esophagus | ESCC | 4.34e-14 | 3.41e-01 | 0.1153 |
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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 |
Esophagus | ESCC | ![]() |
Skin | AK | ![]() |
Skin | SCCIS | ![]() |
Skin | cSCC | ![]() |
Thyroid | HT | ![]() |
∗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:000609120 | Esophagus | HGIN | generation of precursor metabolites and energy | 145/2587 | 490/18723 | 3.41e-20 | 2.04e-17 | 145 |
GO:002290020 | Esophagus | HGIN | electron transport chain | 66/2587 | 175/18723 | 2.21e-15 | 4.73e-13 | 66 |
GO:00162263 | Esophagus | HGIN | iron-sulfur cluster assembly | 10/2587 | 26/18723 | 1.60e-03 | 1.79e-02 | 10 |
GO:00311633 | Esophagus | HGIN | metallo-sulfur cluster assembly | 10/2587 | 26/18723 | 1.60e-03 | 1.79e-02 | 10 |
GO:0006091110 | Esophagus | ESCC | generation of precursor metabolites and energy | 331/8552 | 490/18723 | 3.86e-23 | 8.45e-21 | 331 |
GO:0022900110 | Esophagus | ESCC | electron transport chain | 133/8552 | 175/18723 | 2.18e-16 | 1.67e-14 | 133 |
GO:00067906 | Esophagus | ESCC | sulfur compound metabolic process | 201/8552 | 339/18723 | 2.64e-07 | 3.94e-06 | 201 |
GO:001622611 | Esophagus | ESCC | iron-sulfur cluster assembly | 21/8552 | 26/18723 | 2.69e-04 | 1.63e-03 | 21 |
GO:003116311 | Esophagus | ESCC | metallo-sulfur cluster assembly | 21/8552 | 26/18723 | 2.69e-04 | 1.63e-03 | 21 |
GO:000609122 | Liver | HCC | generation of precursor metabolites and energy | 340/7958 | 490/18723 | 4.04e-34 | 2.85e-31 | 340 |
GO:002290022 | Liver | HCC | electron transport chain | 134/7958 | 175/18723 | 3.32e-20 | 4.68e-18 | 134 |
GO:000679021 | Liver | HCC | sulfur compound metabolic process | 212/7958 | 339/18723 | 5.60e-14 | 3.39e-12 | 212 |
GO:0016226 | Liver | HCC | iron-sulfur cluster assembly | 18/7958 | 26/18723 | 5.37e-03 | 2.24e-02 | 18 |
GO:0031163 | Liver | HCC | metallo-sulfur cluster assembly | 18/7958 | 26/18723 | 5.37e-03 | 2.24e-02 | 18 |
GO:002290018 | Oral cavity | OSCC | electron transport chain | 126/7305 | 175/18723 | 6.65e-19 | 8.42e-17 | 126 |
GO:000609118 | Oral cavity | OSCC | generation of precursor metabolites and energy | 286/7305 | 490/18723 | 1.45e-18 | 1.71e-16 | 286 |
GO:00067905 | Oral cavity | OSCC | sulfur compound metabolic process | 168/7305 | 339/18723 | 4.50e-05 | 3.84e-04 | 168 |
GO:00162262 | Oral cavity | OSCC | iron-sulfur cluster assembly | 19/7305 | 26/18723 | 4.46e-04 | 2.70e-03 | 19 |
GO:00311632 | Oral cavity | OSCC | metallo-sulfur cluster assembly | 19/7305 | 26/18723 | 4.46e-04 | 2.70e-03 | 19 |
GO:002290019 | Oral cavity | LP | electron transport chain | 108/4623 | 175/18723 | 2.21e-25 | 9.90e-23 | 108 |
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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 |
CIAPIN1 | SNV | Missense_Mutation | rs745916329 | c.841N>A | p.Asp281Asn | p.D281N | Q6FI81 | protein_coding | deleterious(0.04) | probably_damaging(0.999) | TCGA-AO-A128-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD |
CIAPIN1 | SNV | Missense_Mutation | c.412G>A | p.Glu138Lys | p.E138K | Q6FI81 | protein_coding | tolerated(0.09) | benign(0.001) | TCGA-DR-A0ZM-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unspecific | Cisplatin | SD | |
CIAPIN1 | SNV | Missense_Mutation | novel | c.729N>T | p.Arg243Ser | p.R243S | Q6FI81 | protein_coding | deleterious(0) | benign(0.355) | TCGA-VS-A9V3-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PD |
CIAPIN1 | SNV | Missense_Mutation | c.458N>G | p.Asn153Ser | p.N153S | Q6FI81 | protein_coding | tolerated(0.88) | benign(0) | TCGA-AA-3815-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
CIAPIN1 | SNV | Missense_Mutation | c.732N>T | p.Lys244Asn | p.K244N | Q6FI81 | protein_coding | deleterious(0) | possibly_damaging(0.575) | TCGA-G4-6304-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Chemotherapy | fluorouracil | PD | |
CIAPIN1 | SNV | Missense_Mutation | rs562918898 | c.697C>T | p.Arg233Trp | p.R233W | Q6FI81 | protein_coding | tolerated(0.09) | benign(0.058) | TCGA-WS-AB45-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CIAPIN1 | SNV | Missense_Mutation | novel | c.512N>A | p.Ser171Tyr | p.S171Y | Q6FI81 | protein_coding | deleterious(0) | possibly_damaging(0.871) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CIAPIN1 | SNV | Missense_Mutation | novel | c.323N>G | p.Lys108Arg | p.K108R | Q6FI81 | protein_coding | tolerated(0.28) | benign(0) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
CIAPIN1 | SNV | Missense_Mutation | novel | c.69G>T | p.Glu23Asp | p.E23D | Q6FI81 | protein_coding | tolerated(0.19) | benign(0) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CIAPIN1 | SNV | Missense_Mutation | novel | c.302N>T | p.Thr101Ile | p.T101I | Q6FI81 | protein_coding | deleterious(0.04) | possibly_damaging(0.74) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | 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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