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Gene: MTHFD2L |
Gene summary for MTHFD2L |
Gene summary. |
Gene information | Species | Human | Gene symbol | MTHFD2L | Gene ID | 441024 |
Gene name | methylenetetrahydrofolate dehydrogenase (NADP+ dependent) 2 like | |
Gene Alias | MTHFD2L | |
Cytomap | 4q13.3 | |
Gene Type | protein-coding | GO ID | GO:0000096 | UniProtAcc | A0A024RDE0 |
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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 |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
441024 | MTHFD2L | LZE8T | Human | Esophagus | ESCC | 6.47e-06 | 1.05e-01 | 0.067 |
441024 | MTHFD2L | LZE24T | Human | Esophagus | ESCC | 2.60e-05 | 1.52e-01 | 0.0596 |
441024 | MTHFD2L | LZE6T | Human | Esophagus | ESCC | 4.96e-10 | 6.96e-01 | 0.0845 |
441024 | MTHFD2L | P1T-E | Human | Esophagus | ESCC | 3.72e-06 | 2.76e-01 | 0.0875 |
441024 | MTHFD2L | P2T-E | Human | Esophagus | ESCC | 9.80e-11 | 3.00e-01 | 0.1177 |
441024 | MTHFD2L | P4T-E | Human | Esophagus | ESCC | 1.23e-21 | 5.47e-01 | 0.1323 |
441024 | MTHFD2L | P5T-E | Human | Esophagus | ESCC | 5.91e-09 | 1.37e-01 | 0.1327 |
441024 | MTHFD2L | P8T-E | Human | Esophagus | ESCC | 4.31e-23 | 2.96e-01 | 0.0889 |
441024 | MTHFD2L | P9T-E | Human | Esophagus | ESCC | 3.68e-07 | 1.45e-01 | 0.1131 |
441024 | MTHFD2L | P10T-E | Human | Esophagus | ESCC | 3.07e-12 | 3.18e-01 | 0.116 |
441024 | MTHFD2L | P11T-E | Human | Esophagus | ESCC | 8.47e-07 | 5.24e-01 | 0.1426 |
441024 | MTHFD2L | P12T-E | Human | Esophagus | ESCC | 1.51e-19 | 2.35e-01 | 0.1122 |
441024 | MTHFD2L | P15T-E | Human | Esophagus | ESCC | 7.28e-10 | 2.12e-01 | 0.1149 |
441024 | MTHFD2L | P16T-E | Human | Esophagus | ESCC | 5.56e-14 | 3.21e-01 | 0.1153 |
441024 | MTHFD2L | P17T-E | Human | Esophagus | ESCC | 2.39e-04 | 2.05e-01 | 0.1278 |
441024 | MTHFD2L | P21T-E | Human | Esophagus | ESCC | 9.93e-52 | 1.20e+00 | 0.1617 |
441024 | MTHFD2L | P22T-E | Human | Esophagus | ESCC | 1.14e-15 | 2.11e-01 | 0.1236 |
441024 | MTHFD2L | P23T-E | Human | Esophagus | ESCC | 1.38e-25 | 6.04e-01 | 0.108 |
441024 | MTHFD2L | P24T-E | Human | Esophagus | ESCC | 9.75e-14 | 1.84e-01 | 0.1287 |
441024 | MTHFD2L | P26T-E | Human | Esophagus | ESCC | 2.43e-31 | 5.45e-01 | 0.1276 |
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Transcriptomic changes along malignancy continuum. |
∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
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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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00000961 | Liver | Cirrhotic | sulfur amino acid metabolic process | 19/4634 | 34/18723 | 1.01e-04 | 1.05e-03 | 19 |
GO:00091654 | Liver | Cirrhotic | nucleotide biosynthetic process | 89/4634 | 254/18723 | 1.45e-04 | 1.40e-03 | 89 |
GO:19012934 | Liver | Cirrhotic | nucleoside phosphate biosynthetic process | 89/4634 | 256/18723 | 1.97e-04 | 1.82e-03 | 89 |
GO:00725225 | Liver | Cirrhotic | purine-containing compound biosynthetic process | 69/4634 | 200/18723 | 1.22e-03 | 8.24e-03 | 69 |
GO:00061645 | Liver | Cirrhotic | purine nucleotide biosynthetic process | 65/4634 | 191/18723 | 2.42e-03 | 1.46e-02 | 65 |
GO:00090661 | Liver | Cirrhotic | aspartate family amino acid metabolic process | 21/4634 | 49/18723 | 4.13e-03 | 2.21e-02 | 21 |
GO:00090671 | Liver | Cirrhotic | aspartate family amino acid biosynthetic process | 11/4634 | 21/18723 | 5.89e-03 | 2.95e-02 | 11 |
GO:00067303 | Liver | Cirrhotic | one-carbon metabolic process | 17/4634 | 40/18723 | 1.04e-02 | 4.61e-02 | 17 |
GO:000911722 | Liver | HCC | nucleotide metabolic process | 300/7958 | 489/18723 | 1.61e-17 | 1.71e-15 | 300 |
GO:000675322 | Liver | HCC | nucleoside phosphate metabolic process | 304/7958 | 497/18723 | 1.78e-17 | 1.85e-15 | 304 |
GO:001605321 | Liver | HCC | organic acid biosynthetic process | 200/7958 | 316/18723 | 5.24e-14 | 3.22e-12 | 200 |
GO:000679021 | Liver | HCC | sulfur compound metabolic process | 212/7958 | 339/18723 | 5.60e-14 | 3.39e-12 | 212 |
GO:004639421 | Liver | HCC | carboxylic acid biosynthetic process | 198/7958 | 314/18723 | 1.19e-13 | 6.78e-12 | 198 |
GO:007252122 | Liver | HCC | purine-containing compound metabolic process | 250/7958 | 416/18723 | 2.26e-13 | 1.24e-11 | 250 |
GO:000616322 | Liver | HCC | purine nucleotide metabolic process | 236/7958 | 396/18723 | 3.59e-12 | 1.62e-10 | 236 |
GO:00086522 | Liver | HCC | cellular amino acid biosynthetic process | 58/7958 | 76/18723 | 1.98e-09 | 5.63e-08 | 58 |
GO:19016052 | Liver | HCC | alpha-amino acid metabolic process | 124/7958 | 195/18723 | 2.07e-09 | 5.79e-08 | 124 |
GO:19016072 | Liver | HCC | alpha-amino acid biosynthetic process | 53/7958 | 68/18723 | 2.62e-09 | 7.16e-08 | 53 |
GO:000657521 | Liver | HCC | cellular modified amino acid metabolic process | 119/7958 | 188/18723 | 6.47e-09 | 1.67e-07 | 119 |
GO:00436482 | Liver | HCC | dicarboxylic acid metabolic process | 68/7958 | 96/18723 | 1.73e-08 | 4.14e-07 | 68 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa012405 | Esophagus | ESCC | Biosynthesis of cofactors | 97/4205 | 153/8465 | 3.88e-04 | 1.35e-03 | 6.94e-04 | 97 |
hsa0124012 | Esophagus | ESCC | Biosynthesis of cofactors | 97/4205 | 153/8465 | 3.88e-04 | 1.35e-03 | 6.94e-04 | 97 |
hsa01240 | Liver | Cirrhotic | Biosynthesis of cofactors | 66/2530 | 153/8465 | 3.11e-04 | 1.99e-03 | 1.23e-03 | 66 |
hsa012401 | Liver | Cirrhotic | Biosynthesis of cofactors | 66/2530 | 153/8465 | 3.11e-04 | 1.99e-03 | 1.23e-03 | 66 |
hsa012402 | Liver | HCC | Biosynthesis of cofactors | 103/4020 | 153/8465 | 4.67e-07 | 5.05e-06 | 2.81e-06 | 103 |
hsa006702 | Liver | HCC | One carbon pool by folate | 17/4020 | 20/8465 | 6.04e-04 | 2.50e-03 | 1.39e-03 | 17 |
hsa012403 | Liver | HCC | Biosynthesis of cofactors | 103/4020 | 153/8465 | 4.67e-07 | 5.05e-06 | 2.81e-06 | 103 |
hsa0067011 | Liver | HCC | One carbon pool by folate | 17/4020 | 20/8465 | 6.04e-04 | 2.50e-03 | 1.39e-03 | 17 |
hsa012404 | Oral cavity | OSCC | Biosynthesis of cofactors | 88/3704 | 153/8465 | 3.84e-04 | 1.20e-03 | 6.12e-04 | 88 |
hsa0124011 | Oral cavity | OSCC | Biosynthesis of cofactors | 88/3704 | 153/8465 | 3.84e-04 | 1.20e-03 | 6.12e-04 | 88 |
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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 |
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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. |
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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 |
MTHFD2L | SNV | Missense_Mutation | rs765684065 | c.808A>G | p.Ile270Val | p.I270V | Q9H903 | protein_coding | tolerated(0.62) | benign(0.163) | TCGA-A8-A08C-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | 5-fluorouracil | CR |
MTHFD2L | SNV | Missense_Mutation | novel | c.740G>T | p.Arg247Ile | p.R247I | Q9H903 | protein_coding | deleterious(0.02) | probably_damaging(0.995) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
MTHFD2L | SNV | Missense_Mutation | rs779291421 | c.275N>C | p.Asn92Thr | p.N92T | Q9H903 | protein_coding | deleterious(0) | possibly_damaging(0.793) | TCGA-C5-A1M7-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
MTHFD2L | SNV | Missense_Mutation | rs775868972 | c.703N>T | p.Arg235Trp | p.R235W | Q9H903 | protein_coding | deleterious(0.02) | probably_damaging(0.995) | TCGA-FU-A3TQ-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unknown | Unknown | SD |
MTHFD2L | deletion | Frame_Shift_Del | rs761538540 | c.1033delA | p.Ile345SerfsTer48 | p.I345Sfs*48 | Q9H903 | protein_coding | TCGA-MA-AA42-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | ||
MTHFD2L | SNV | Missense_Mutation | rs761954094 | c.467N>A | p.Arg156Gln | p.R156Q | Q9H903 | protein_coding | tolerated(0.25) | probably_damaging(0.998) | TCGA-AD-6895-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
MTHFD2L | SNV | Missense_Mutation | novel | c.1000N>T | p.Leu334Phe | p.L334F | Q9H903 | protein_coding | deleterious(0) | probably_damaging(0.974) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
MTHFD2L | SNV | Missense_Mutation | rs575932490 | c.172N>A | p.Glu58Lys | p.E58K | Q9H903 | protein_coding | tolerated(1) | benign(0.006) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | CR |
MTHFD2L | SNV | Missense_Mutation | c.578N>T | p.Ala193Val | p.A193V | Q9H903 | protein_coding | deleterious(0) | probably_damaging(0.911) | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
MTHFD2L | deletion | Frame_Shift_Del | rs761538540 | c.1033delA | p.Ile345SerfsTer48 | p.I345Sfs*48 | Q9H903 | protein_coding | TCGA-A6-6781-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | SD |
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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 |
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