![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: TCAF1 |
Gene summary for TCAF1 |
![]() |
Gene information | Species | Human | Gene symbol | TCAF1 | Gene ID | 9747 |
Gene name | TRPM8 channel associated factor 1 | |
Gene Alias | FAM115A | |
Cytomap | 7q35 | |
Gene Type | protein-coding | GO ID | GO:0006605 | UniProtAcc | Q9Y4C2 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
9747 | TCAF1 | HTA11_1938_2000001011 | Human | Colorectum | AD | 4.04e-03 | 2.85e-01 | -0.0811 |
9747 | TCAF1 | HTA11_78_2000001011 | Human | Colorectum | AD | 1.99e-11 | 4.91e-01 | -0.1088 |
9747 | TCAF1 | HTA11_347_2000001011 | Human | Colorectum | AD | 7.36e-20 | 5.34e-01 | -0.1954 |
9747 | TCAF1 | HTA11_1391_2000001011 | Human | Colorectum | AD | 2.83e-10 | 4.55e-01 | -0.059 |
9747 | TCAF1 | HTA11_99999965104_69814 | Human | Colorectum | MSS | 2.93e-06 | 4.50e-01 | 0.281 |
9747 | TCAF1 | A015-C-203 | Human | Colorectum | FAP | 7.28e-05 | -1.10e-01 | -0.1294 |
9747 | TCAF1 | A015-C-104 | Human | Colorectum | FAP | 1.00e-04 | -6.44e-02 | -0.1899 |
9747 | TCAF1 | A002-C-116 | Human | Colorectum | FAP | 4.39e-06 | -4.74e-02 | -0.0452 |
9747 | TCAF1 | F072B | Human | Colorectum | FAP | 3.34e-02 | 3.97e-01 | 0.257 |
9747 | TCAF1 | CRC-3-11773 | Human | Colorectum | CRC | 8.23e-03 | -1.19e-01 | 0.2564 |
9747 | TCAF1 | LZE2T | Human | Esophagus | ESCC | 1.80e-02 | 5.54e-01 | 0.082 |
9747 | TCAF1 | LZE4T | Human | Esophagus | ESCC | 1.58e-04 | 2.07e-01 | 0.0811 |
9747 | TCAF1 | LZE7T | Human | Esophagus | ESCC | 3.18e-07 | 3.61e-01 | 0.0667 |
9747 | TCAF1 | LZE8T | Human | Esophagus | ESCC | 9.22e-05 | 1.90e-01 | 0.067 |
9747 | TCAF1 | LZE20T | Human | Esophagus | ESCC | 8.90e-06 | 1.43e-01 | 0.0662 |
9747 | TCAF1 | LZE22T | Human | Esophagus | ESCC | 6.92e-04 | 2.54e-01 | 0.068 |
9747 | TCAF1 | LZE24T | Human | Esophagus | ESCC | 5.37e-12 | 3.13e-01 | 0.0596 |
9747 | TCAF1 | P1T-E | Human | Esophagus | ESCC | 2.61e-08 | 2.94e-01 | 0.0875 |
9747 | TCAF1 | P2T-E | Human | Esophagus | ESCC | 8.33e-15 | 2.60e-01 | 0.1177 |
9747 | TCAF1 | P4T-E | Human | Esophagus | ESCC | 2.52e-17 | 3.55e-01 | 0.1323 |
Page: 1 2 3 4 5 6 |
![]() |
∗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. |
Top |
Malignant transformation related pathway analysis |
![]() |
![]() |
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). |
Page: 1 2 3 4 5 6 7 8 9 |
![]() |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:1903829 | Colorectum | AD | positive regulation of cellular protein localization | 110/3918 | 276/18723 | 4.58e-13 | 8.44e-11 | 110 |
GO:0090150 | Colorectum | AD | establishment of protein localization to membrane | 100/3918 | 260/18723 | 6.01e-11 | 6.33e-09 | 100 |
GO:1905475 | Colorectum | AD | regulation of protein localization to membrane | 73/3918 | 175/18723 | 3.37e-10 | 2.93e-08 | 73 |
GO:1904951 | Colorectum | AD | positive regulation of establishment of protein localization | 112/3918 | 319/18723 | 2.55e-09 | 1.80e-07 | 112 |
GO:0051222 | Colorectum | AD | positive regulation of protein transport | 106/3918 | 303/18723 | 8.45e-09 | 5.08e-07 | 106 |
GO:0006605 | Colorectum | AD | protein targeting | 105/3918 | 314/18723 | 1.39e-07 | 6.44e-06 | 105 |
GO:1905477 | Colorectum | AD | positive regulation of protein localization to membrane | 46/3918 | 106/18723 | 1.47e-07 | 6.64e-06 | 46 |
GO:0090316 | Colorectum | AD | positive regulation of intracellular protein transport | 62/3918 | 160/18723 | 1.82e-07 | 7.79e-06 | 62 |
GO:0032388 | Colorectum | AD | positive regulation of intracellular transport | 74/3918 | 202/18723 | 1.83e-07 | 7.80e-06 | 74 |
GO:0032386 | Colorectum | AD | regulation of intracellular transport | 109/3918 | 337/18723 | 5.33e-07 | 1.95e-05 | 109 |
GO:0033157 | Colorectum | AD | regulation of intracellular protein transport | 80/3918 | 229/18723 | 5.81e-07 | 2.09e-05 | 80 |
GO:1903533 | Colorectum | AD | regulation of protein targeting | 31/3918 | 81/18723 | 2.61e-04 | 3.25e-03 | 31 |
GO:0032411 | Colorectum | AD | positive regulation of transporter activity | 37/3918 | 120/18723 | 6.82e-03 | 4.22e-02 | 37 |
GO:19038292 | Colorectum | MSS | positive regulation of cellular protein localization | 103/3467 | 276/18723 | 1.12e-13 | 2.67e-11 | 103 |
GO:19049512 | Colorectum | MSS | positive regulation of establishment of protein localization | 110/3467 | 319/18723 | 6.30e-12 | 9.83e-10 | 110 |
GO:00512222 | Colorectum | MSS | positive regulation of protein transport | 104/3467 | 303/18723 | 3.23e-11 | 4.11e-09 | 104 |
GO:19054752 | Colorectum | MSS | regulation of protein localization to membrane | 68/3467 | 175/18723 | 2.16e-10 | 2.09e-08 | 68 |
GO:00901502 | Colorectum | MSS | establishment of protein localization to membrane | 90/3467 | 260/18723 | 4.11e-10 | 3.49e-08 | 90 |
GO:00903162 | Colorectum | MSS | positive regulation of intracellular protein transport | 60/3467 | 160/18723 | 1.18e-08 | 7.08e-07 | 60 |
GO:00323882 | Colorectum | MSS | positive regulation of intracellular transport | 70/3467 | 202/18723 | 3.32e-08 | 1.82e-06 | 70 |
Page: 1 2 3 4 5 6 7 8 9 10 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
Top |
Cell-cell communication analysis |
![]() |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
![]() |
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. |
Page: 1 |
Top |
Somatic mutation of malignant transformation related genes |
![]() |
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 |
TCAF1 | SNV | Missense_Mutation | novel | c.82N>A | p.Glu28Lys | p.E28K | Q9Y4C2 | protein_coding | tolerated(0.14) | benign(0.348) | TCGA-E2-A2P6-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | anastrozole | SD |
TCAF1 | SNV | Missense_Mutation | novel | c.2299G>A | p.Glu767Lys | p.E767K | Q9Y4C2 | protein_coding | tolerated(0.17) | benign(0.028) | TCGA-EA-A3HS-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
TCAF1 | SNV | Missense_Mutation | c.276N>G | p.Ile92Met | p.I92M | Q9Y4C2 | protein_coding | deleterious(0.02) | benign(0.271) | TCGA-CA-6718-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
TCAF1 | SNV | Missense_Mutation | rs149141329 | c.167N>A | p.Arg56His | p.R56H | Q9Y4C2 | protein_coding | tolerated(0.07) | benign(0.006) | TCGA-CM-4746-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
TCAF1 | SNV | Missense_Mutation | novel | c.316G>A | p.Glu106Lys | p.E106K | Q9Y4C2 | protein_coding | tolerated(0.93) | benign(0.005) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
TCAF1 | SNV | Missense_Mutation | rs373629994 | c.25G>A | p.Glu9Lys | p.E9K | Q9Y4C2 | protein_coding | tolerated(0.1) | benign(0.117) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TCAF1 | SNV | Missense_Mutation | novel | c.295N>A | p.Ala99Thr | p.A99T | Q9Y4C2 | protein_coding | tolerated(0.55) | benign(0.003) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
TCAF1 | SNV | Missense_Mutation | novel | c.2613N>T | p.Lys871Asn | p.K871N | Q9Y4C2 | protein_coding | deleterious(0.01) | possibly_damaging(0.701) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TCAF1 | SNV | Missense_Mutation | novel | c.2312C>T | p.Pro771Leu | p.P771L | Q9Y4C2 | protein_coding | deleterious(0.02) | probably_damaging(0.976) | TCGA-AP-A1DH-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TCAF1 | SNV | Missense_Mutation | novel | c.2701N>A | p.Ala901Thr | p.A901T | Q9Y4C2 | protein_coding | deleterious(0.04) | possibly_damaging(0.758) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 4 5 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |