![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: TMEM19 |
Gene summary for TMEM19 |
![]() |
Gene information | Species | Human | Gene symbol | TMEM19 | Gene ID | 55266 |
Gene name | transmembrane protein 19 | |
Gene Alias | TMEM19 | |
Cytomap | 12q21.1 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | A0A024RBA1 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55266 | TMEM19 | SYSMH2 | Human | Oral cavity | OSCC | 1.08e-07 | 2.47e-01 | 0.2326 |
55266 | TMEM19 | SYSMH3 | Human | Oral cavity | OSCC | 2.19e-07 | 2.72e-01 | 0.2442 |
55266 | TMEM19 | P1_cSCC | Human | Skin | cSCC | 1.59e-10 | 3.80e-01 | 0.0292 |
55266 | TMEM19 | P2_cSCC | Human | Skin | cSCC | 4.08e-06 | 2.38e-01 | -0.024 |
55266 | TMEM19 | P4_cSCC | Human | Skin | cSCC | 1.69e-11 | 3.44e-01 | -0.00290000000000005 |
55266 | TMEM19 | P10_cSCC | Human | Skin | cSCC | 1.16e-23 | 6.33e-01 | 0.1017 |
55266 | TMEM19 | male-WTA | Human | Thyroid | PTC | 7.76e-08 | 6.70e-02 | 0.1037 |
55266 | TMEM19 | PTC01 | Human | Thyroid | PTC | 1.03e-03 | 4.11e-03 | 0.1899 |
55266 | TMEM19 | PTC05 | Human | Thyroid | PTC | 2.51e-02 | 1.33e-01 | 0.2065 |
55266 | TMEM19 | PTC06 | Human | Thyroid | PTC | 3.66e-08 | 1.75e-01 | 0.2057 |
55266 | TMEM19 | PTC07 | Human | Thyroid | PTC | 1.62e-08 | 2.95e-02 | 0.2044 |
55266 | TMEM19 | ATC12 | Human | Thyroid | ATC | 2.47e-10 | 1.65e-01 | 0.34 |
55266 | TMEM19 | ATC13 | Human | Thyroid | ATC | 5.11e-55 | 1.31e+00 | 0.34 |
55266 | TMEM19 | ATC2 | Human | Thyroid | ATC | 7.40e-09 | 7.52e-01 | 0.34 |
55266 | TMEM19 | ATC4 | Human | Thyroid | ATC | 1.11e-10 | 2.19e-01 | 0.34 |
55266 | TMEM19 | ATC5 | Human | Thyroid | ATC | 4.28e-52 | 1.48e+00 | 0.34 |
Page: 1 2 3 4 5 |
![]() |
∗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:000703314 | Esophagus | ESCC | vacuole organization | 127/8552 | 180/18723 | 1.04e-11 | 3.85e-10 | 127 |
GO:0070482111 | Esophagus | ESCC | response to oxygen levels | 218/8552 | 347/18723 | 6.91e-11 | 2.17e-09 | 218 |
GO:0071453110 | Esophagus | ESCC | cellular response to oxygen levels | 114/8552 | 177/18723 | 3.63e-07 | 5.06e-06 | 114 |
GO:00070403 | Esophagus | ESCC | lysosome organization | 53/8552 | 74/18723 | 5.34e-06 | 5.57e-05 | 53 |
GO:00801713 | Esophagus | ESCC | lytic vacuole organization | 53/8552 | 74/18723 | 5.34e-06 | 5.57e-05 | 53 |
GO:005507617 | Esophagus | ESCC | transition metal ion homeostasis | 87/8552 | 138/18723 | 2.85e-05 | 2.37e-04 | 87 |
GO:00070353 | Esophagus | ESCC | vacuolar acidification | 20/8552 | 24/18723 | 1.69e-04 | 1.11e-03 | 20 |
GO:00070423 | Esophagus | ESCC | lysosomal lumen acidification | 11/8552 | 11/18723 | 1.80e-04 | 1.16e-03 | 11 |
GO:00070393 | Esophagus | ESCC | protein catabolic process in the vacuole | 16/8552 | 19/18723 | 6.45e-04 | 3.43e-03 | 16 |
GO:00469169 | Esophagus | ESCC | cellular transition metal ion homeostasis | 70/8552 | 115/18723 | 7.28e-04 | 3.79e-03 | 70 |
GO:19051463 | Esophagus | ESCC | lysosomal protein catabolic process | 13/8552 | 15/18723 | 1.31e-03 | 6.26e-03 | 13 |
GO:00514521 | Esophagus | ESCC | intracellular pH reduction | 29/8552 | 42/18723 | 1.87e-03 | 8.46e-03 | 29 |
GO:00458511 | Esophagus | ESCC | pH reduction | 31/8552 | 46/18723 | 2.42e-03 | 1.06e-02 | 31 |
GO:00550729 | Esophagus | ESCC | iron ion homeostasis | 52/8552 | 85/18723 | 2.86e-03 | 1.21e-02 | 52 |
GO:00700711 | Esophagus | ESCC | proton-transporting two-sector ATPase complex assembly | 12/8552 | 15/18723 | 7.31e-03 | 2.63e-02 | 12 |
GO:00070332 | Liver | Cirrhotic | vacuole organization | 80/4634 | 180/18723 | 5.73e-09 | 2.25e-07 | 80 |
GO:00704827 | Liver | Cirrhotic | response to oxygen levels | 125/4634 | 347/18723 | 1.55e-06 | 3.02e-05 | 125 |
GO:00550766 | Liver | Cirrhotic | transition metal ion homeostasis | 59/4634 | 138/18723 | 2.59e-06 | 4.65e-05 | 59 |
GO:0007040 | Liver | Cirrhotic | lysosome organization | 35/4634 | 74/18723 | 2.10e-05 | 2.77e-04 | 35 |
GO:0080171 | Liver | Cirrhotic | lytic vacuole organization | 35/4634 | 74/18723 | 2.10e-05 | 2.77e-04 | 35 |
Page: 1 2 3 4 5 |
![]() |
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 |
TMEM19 | SNV | Missense_Mutation | c.433N>A | p.Glu145Lys | p.E145K | Q96HH6 | protein_coding | deleterious(0.01) | possibly_damaging(0.575) | TCGA-A2-A0CX-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | |
TMEM19 | SNV | Missense_Mutation | c.938N>C | p.Val313Ala | p.V313A | Q96HH6 | protein_coding | deleterious(0) | probably_damaging(0.953) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD | |
TMEM19 | insertion | Frame_Shift_Ins | novel | c.970_971insGTGAAACCCCATCTCTACTAAAAATACAAAAATTATC | p.Leu324CysfsTer41 | p.L324Cfs*41 | Q96HH6 | protein_coding | TCGA-A8-A09D-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | CR | ||
TMEM19 | SNV | Missense_Mutation | rs185566519 | c.472G>A | p.Glu158Lys | p.E158K | Q96HH6 | protein_coding | deleterious(0) | possibly_damaging(0.575) | TCGA-C5-A8XJ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | SD |
TMEM19 | SNV | Missense_Mutation | novel | c.886N>T | p.Thr296Ser | p.T296S | Q96HH6 | protein_coding | tolerated(0.38) | benign(0) | TCGA-AA-A01K-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | folinic | CR |
TMEM19 | SNV | Missense_Mutation | novel | c.111N>T | p.Met37Ile | p.M37I | Q96HH6 | protein_coding | tolerated(0.69) | benign(0) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
TMEM19 | SNV | Missense_Mutation | c.727N>T | p.Ile243Phe | p.I243F | Q96HH6 | protein_coding | tolerated(0.3) | benign(0.104) | TCGA-F4-6570-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
TMEM19 | SNV | Missense_Mutation | novel | c.586N>A | p.Leu196Met | p.L196M | Q96HH6 | protein_coding | tolerated(0.18) | benign(0.133) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
TMEM19 | SNV | Missense_Mutation | novel | c.449N>G | p.Tyr150Cys | p.Y150C | Q96HH6 | protein_coding | deleterious(0) | possibly_damaging(0.866) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TMEM19 | SNV | Missense_Mutation | c.899N>T | p.Arg300Met | p.R300M | Q96HH6 | protein_coding | deleterious(0) | benign(0.183) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
Page: 1 2 3 |
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 |