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Gene: NFIC |
Gene summary for NFIC |
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Gene information | Species | Human | Gene symbol | NFIC | Gene ID | 4782 |
Gene name | nuclear factor I C | |
Gene Alias | CTF | |
Cytomap | 19p13.3 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | B7Z4T6 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
4782 | NFIC | GSM4909296 | Human | Breast | IDC | 4.73e-10 | 2.08e-01 | 0.1524 |
4782 | NFIC | GSM4909297 | Human | Breast | IDC | 5.16e-10 | -1.60e-01 | 0.1517 |
4782 | NFIC | GSM4909298 | Human | Breast | IDC | 3.82e-05 | 2.92e-01 | 0.1551 |
4782 | NFIC | GSM4909302 | Human | Breast | IDC | 6.99e-04 | 2.85e-01 | 0.1545 |
4782 | NFIC | GSM4909303 | Human | Breast | IDC | 8.84e-04 | 4.91e-01 | 0.0438 |
4782 | NFIC | GSM4909306 | Human | Breast | IDC | 8.17e-03 | 2.67e-01 | 0.1564 |
4782 | NFIC | GSM4909308 | Human | Breast | IDC | 2.37e-04 | 3.24e-01 | 0.158 |
4782 | NFIC | GSM4909311 | Human | Breast | IDC | 1.11e-22 | -1.70e-01 | 0.1534 |
4782 | NFIC | GSM4909312 | Human | Breast | IDC | 6.91e-08 | 9.45e-02 | 0.1552 |
4782 | NFIC | GSM4909313 | Human | Breast | IDC | 6.42e-03 | 1.95e-01 | 0.0391 |
4782 | NFIC | GSM4909319 | Human | Breast | IDC | 1.16e-40 | -5.27e-02 | 0.1563 |
4782 | NFIC | GSM4909320 | Human | Breast | IDC | 8.32e-03 | -2.76e-01 | 0.1575 |
4782 | NFIC | GSM4909321 | Human | Breast | IDC | 1.03e-15 | 1.59e-02 | 0.1559 |
4782 | NFIC | brca3 | Human | Breast | Precancer | 9.68e-03 | 2.25e-01 | -0.0263 |
4782 | NFIC | M5 | Human | Breast | IDC | 3.58e-09 | 7.60e-01 | 0.1598 |
4782 | NFIC | NCCBC14 | Human | Breast | DCIS | 1.56e-07 | 1.03e-01 | 0.2021 |
4782 | NFIC | NCCBC3 | Human | Breast | DCIS | 1.36e-03 | 1.06e-01 | 0.1198 |
4782 | NFIC | NCCBC5 | Human | Breast | DCIS | 7.82e-08 | -4.52e-02 | 0.2046 |
4782 | NFIC | NCCBC6 | Human | Breast | DCIS | 8.80e-08 | 4.89e-01 | 0.2095 |
4782 | NFIC | P1 | Human | Breast | IDC | 1.90e-15 | 4.36e-02 | 0.1527 |
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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:0006260 | Colorectum | MSI-H | DNA replication | 31/1319 | 260/18723 | 2.83e-03 | 3.63e-02 | 31 |
GO:00062604 | Esophagus | ESCC | DNA replication | 181/8552 | 260/18723 | 3.55e-15 | 2.05e-13 | 181 |
GO:00062601 | Liver | HCC | DNA replication | 146/7958 | 260/18723 | 5.68e-06 | 7.02e-05 | 146 |
GO:00062603 | Oral cavity | OSCC | DNA replication | 159/7305 | 260/18723 | 3.25e-13 | 1.59e-11 | 159 |
GO:000626011 | Oral cavity | LP | DNA replication | 97/4623 | 260/18723 | 3.67e-06 | 7.75e-05 | 97 |
GO:00062605 | Skin | AK | DNA replication | 40/1910 | 260/18723 | 5.49e-03 | 3.03e-02 | 40 |
GO:000626012 | Skin | cSCC | DNA replication | 106/4864 | 260/18723 | 1.18e-07 | 2.77e-06 | 106 |
GO:00062606 | Thyroid | PTC | DNA replication | 114/5968 | 260/18723 | 3.09e-05 | 2.95e-04 | 114 |
GO:000626013 | Thyroid | ATC | DNA replication | 124/6293 | 260/18723 | 1.58e-06 | 1.93e-05 | 124 |
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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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∗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 |
NFIC | SNV | Missense_Mutation | c.1234N>G | p.Leu412Val | p.L412V | P08651 | protein_coding | deleterious(0.04) | probably_damaging(0.994) | TCGA-AR-A0U0-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
NFIC | SNV | Missense_Mutation | c.515N>T | p.Ala172Val | p.A172V | P08651 | protein_coding | tolerated(0.06) | benign(0.19) | TCGA-BH-A0B5-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | CR | |
NFIC | SNV | Missense_Mutation | rs564835230 | c.1438N>A | p.Asp480Asn | p.D480N | P08651 | protein_coding | deleterious(0.01) | benign(0) | TCGA-BH-A1F8-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
NFIC | deletion | Frame_Shift_Del | novel | c.298delN | p.Lys100ArgfsTer141 | p.K100Rfs*141 | P08651 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | ||
NFIC | SNV | Missense_Mutation | c.44N>T | p.Pro15Leu | p.P15L | P08651 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
NFIC | SNV | Missense_Mutation | novel | c.210N>C | p.Gln70His | p.Q70H | P08651 | protein_coding | deleterious(0.01) | probably_damaging(0.996) | TCGA-HM-A4S6-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | cisplatin | CR |
NFIC | SNV | Missense_Mutation | novel | c.857N>T | p.Ser286Leu | p.S286L | P08651 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-VS-A8EL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
NFIC | SNV | Missense_Mutation | novel | c.725G>A | p.Gly242Glu | p.G242E | P08651 | protein_coding | deleterious(0.01) | probably_damaging(0.934) | TCGA-ZJ-AAXB-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
NFIC | SNV | Missense_Mutation | c.919N>T | p.Thr307Ser | p.T307S | P08651 | protein_coding | tolerated(0.71) | benign(0.138) | TCGA-A6-4105-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
NFIC | SNV | Missense_Mutation | rs757507471 | c.706N>T | p.Arg236Trp | p.R236W | P08651 | protein_coding | deleterious(0) | possibly_damaging(0.745) | TCGA-AA-3492-01 | 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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