|
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: SEPT7 |
Gene summary for SEPT7 |
| Gene information | Species | Human | Gene symbol | SEPT7 | Gene ID | 989 |
| Gene name | septin 7 | |
| Gene Alias | CDC10 | |
| Cytomap | 7p14.2 | |
| Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | A8K3D0 |
Top |
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 |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 989 | SEPT7 | HTA11_3410_2000001011 | Human | Colorectum | AD | 2.86e-28 | -6.56e-01 | 0.0155 |
| 989 | SEPT7 | HTA11_2487_2000001011 | Human | Colorectum | SER | 6.85e-17 | -6.56e-01 | -0.1808 |
| 989 | SEPT7 | HTA11_2951_2000001011 | Human | Colorectum | AD | 1.39e-03 | -6.56e-01 | 0.0216 |
| 989 | SEPT7 | HTA11_1938_2000001011 | Human | Colorectum | AD | 7.35e-13 | -6.56e-01 | -0.0811 |
| 989 | SEPT7 | HTA11_78_2000001011 | Human | Colorectum | AD | 7.65e-20 | -6.56e-01 | -0.1088 |
| 989 | SEPT7 | HTA11_347_2000001011 | Human | Colorectum | AD | 2.60e-30 | -6.56e-01 | -0.1954 |
| 989 | SEPT7 | HTA11_2112_2000001011 | Human | Colorectum | SER | 5.87e-03 | -6.56e-01 | -0.2196 |
| 989 | SEPT7 | HTA11_3361_2000001011 | Human | Colorectum | AD | 2.35e-13 | -6.56e-01 | -0.1207 |
| 989 | SEPT7 | HTA11_83_2000001011 | Human | Colorectum | SER | 1.08e-10 | -6.56e-01 | -0.1526 |
| 989 | SEPT7 | HTA11_696_2000001011 | Human | Colorectum | AD | 4.51e-40 | -6.56e-01 | -0.1464 |
| 989 | SEPT7 | HTA11_866_2000001011 | Human | Colorectum | AD | 4.51e-40 | -6.56e-01 | -0.1001 |
| 989 | SEPT7 | HTA11_1391_2000001011 | Human | Colorectum | AD | 5.31e-23 | -6.56e-01 | -0.059 |
| 989 | SEPT7 | HTA11_2992_2000001011 | Human | Colorectum | SER | 8.29e-05 | -6.56e-01 | -0.1706 |
| 989 | SEPT7 | HTA11_5212_2000001011 | Human | Colorectum | AD | 1.06e-05 | -6.56e-01 | -0.2061 |
| 989 | SEPT7 | HTA11_5216_2000001011 | Human | Colorectum | SER | 1.39e-03 | -6.56e-01 | -0.1462 |
| 989 | SEPT7 | HTA11_546_2000001011 | Human | Colorectum | AD | 3.14e-09 | -6.56e-01 | -0.0842 |
| 989 | SEPT7 | HTA11_7862_2000001011 | Human | Colorectum | AD | 1.97e-07 | -6.56e-01 | -0.0179 |
| 989 | SEPT7 | HTA11_866_3004761011 | Human | Colorectum | AD | 5.11e-25 | -6.56e-01 | 0.096 |
| 989 | SEPT7 | HTA11_4255_2000001011 | Human | Colorectum | SER | 1.39e-03 | -6.56e-01 | 0.0446 |
| 989 | SEPT7 | HTA11_9408_2000001011 | Human | Colorectum | AD | 2.54e-02 | -6.56e-01 | 0.0451 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 |
| ∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
| 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 |
| Page: 1 |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa0513120 | Cervix | CC | Shigellosis | 69/1267 | 247/8465 | 7.64e-08 | 1.03e-06 | 6.10e-07 | 69 |
| hsa05131110 | Cervix | CC | Shigellosis | 69/1267 | 247/8465 | 7.64e-08 | 1.03e-06 | 6.10e-07 | 69 |
| hsa05131 | Colorectum | AD | Shigellosis | 109/2092 | 247/8465 | 1.09e-11 | 2.44e-10 | 1.55e-10 | 109 |
| hsa051311 | Colorectum | AD | Shigellosis | 109/2092 | 247/8465 | 1.09e-11 | 2.44e-10 | 1.55e-10 | 109 |
| hsa051312 | Colorectum | SER | Shigellosis | 87/1580 | 247/8465 | 3.07e-10 | 7.27e-09 | 5.28e-09 | 87 |
| hsa051313 | Colorectum | SER | Shigellosis | 87/1580 | 247/8465 | 3.07e-10 | 7.27e-09 | 5.28e-09 | 87 |
| hsa0513126 | Endometrium | AEH | Shigellosis | 78/1197 | 247/8465 | 9.23e-13 | 2.00e-11 | 1.46e-11 | 78 |
| hsa05131111 | Endometrium | AEH | Shigellosis | 78/1197 | 247/8465 | 9.23e-13 | 2.00e-11 | 1.46e-11 | 78 |
| hsa0513127 | Endometrium | EEC | Shigellosis | 79/1237 | 247/8465 | 1.80e-12 | 3.95e-11 | 2.95e-11 | 79 |
| hsa0513136 | Endometrium | EEC | Shigellosis | 79/1237 | 247/8465 | 1.80e-12 | 3.95e-11 | 2.95e-11 | 79 |
| hsa0513139 | Esophagus | HGIN | Shigellosis | 71/1383 | 247/8465 | 4.89e-07 | 7.98e-06 | 6.34e-06 | 71 |
| hsa05131114 | Esophagus | HGIN | Shigellosis | 71/1383 | 247/8465 | 4.89e-07 | 7.98e-06 | 6.34e-06 | 71 |
| hsa05131211 | Esophagus | ESCC | Shigellosis | 176/4205 | 247/8465 | 2.27e-12 | 4.01e-11 | 2.05e-11 | 176 |
| hsa05131310 | Esophagus | ESCC | Shigellosis | 176/4205 | 247/8465 | 2.27e-12 | 4.01e-11 | 2.05e-11 | 176 |
| hsa0513116 | Lung | IAC | Shigellosis | 58/1053 | 247/8465 | 8.21e-07 | 3.81e-05 | 2.53e-05 | 58 |
| hsa0513117 | Lung | IAC | Shigellosis | 58/1053 | 247/8465 | 8.21e-07 | 3.81e-05 | 2.53e-05 | 58 |
| hsa0513123 | Lung | AIS | Shigellosis | 53/961 | 247/8465 | 2.70e-06 | 9.71e-05 | 6.21e-05 | 53 |
| hsa0513133 | Lung | AIS | Shigellosis | 53/961 | 247/8465 | 2.70e-06 | 9.71e-05 | 6.21e-05 | 53 |
| hsa0513143 | Lung | MIAC | Shigellosis | 29/507 | 247/8465 | 3.64e-04 | 7.06e-03 | 5.11e-03 | 29 |
| hsa0513153 | Lung | MIAC | Shigellosis | 29/507 | 247/8465 | 3.64e-04 | 7.06e-03 | 5.11e-03 | 29 |
| Page: 1 2 |
Top |
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 |
| Page: 1 |
Top |
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. |
| Page: 1 |
Top |
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 |
| SEPT7 | SNV | Missense_Mutation | c.827N>A | p.Arg276Lys | p.R276K | protein_coding | tolerated(0.38) | benign(0.011) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | ||
| SEPT7 | insertion | Frame_Shift_Ins | novel | c.840_841insAATTTACTCCCTG | p.Val281AsnfsTer8 | p.V281Nfs*8 | protein_coding | TCGA-AO-A128-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD | |||
| SEPT7 | deletion | Frame_Shift_Del | novel | c.12delN | p.Ser4ArgfsTer27 | p.S4Rfs*27 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | |||
| SEPT7 | SNV | Missense_Mutation | novel | c.895C>T | p.Pro299Ser | p.P299S | protein_coding | deleterious(0.03) | possibly_damaging(0.652) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
| SEPT7 | SNV | Missense_Mutation | novel | c.424N>C | p.Glu142Gln | p.E142Q | protein_coding | deleterious(0.04) | probably_damaging(0.999) | TCGA-C5-A8YQ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | PD | |
| SEPT7 | SNV | Missense_Mutation | c.1018N>C | p.Glu340Gln | p.E340Q | protein_coding | tolerated(0.05) | probably_damaging(0.935) | TCGA-IR-A3LH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | ||
| SEPT7 | SNV | Missense_Mutation | c.692N>G | p.Tyr231Cys | p.Y231C | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-CA-6718-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | PD | ||
| SEPT7 | SNV | Missense_Mutation | rs761757988 | c.1036N>T | p.Arg346Cys | p.R346C | protein_coding | deleterious(0.02) | benign(0.171) | TCGA-G4-6586-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| SEPT7 | SNV | Missense_Mutation | c.1037G>A | p.Arg346His | p.R346H | protein_coding | deleterious(0.03) | benign(0.171) | TCGA-NH-A5IV-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
| SEPT7 | SNV | Missense_Mutation | novel | c.632C>T | p.Ala211Val | p.A211V | protein_coding | deleterious(0) | probably_damaging(0.974) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
| Page: 1 2 3 4 |
Top |
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 |
| Page: 1 |