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Gene: FUNDC1 |
Gene summary for FUNDC1 |
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Gene information | Species | Human | Gene symbol | FUNDC1 | Gene ID | 139341 |
Gene name | FUN14 domain containing 1 | |
Gene Alias | FUNDC1 | |
Cytomap | Xp11.3 | |
Gene Type | protein-coding | GO ID | GO:0000422 | UniProtAcc | Q8IVP5 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
139341 | FUNDC1 | LZE4T | Human | Esophagus | ESCC | 7.31e-13 | 3.40e-01 | 0.0811 |
139341 | FUNDC1 | LZE20T | Human | Esophagus | ESCC | 2.42e-02 | 1.71e-01 | 0.0662 |
139341 | FUNDC1 | LZE24T | Human | Esophagus | ESCC | 1.36e-07 | 2.33e-01 | 0.0596 |
139341 | FUNDC1 | LZE21T | Human | Esophagus | ESCC | 2.09e-04 | 2.41e-01 | 0.0655 |
139341 | FUNDC1 | P1T-E | Human | Esophagus | ESCC | 3.18e-04 | 3.40e-01 | 0.0875 |
139341 | FUNDC1 | P2T-E | Human | Esophagus | ESCC | 1.98e-23 | 5.08e-01 | 0.1177 |
139341 | FUNDC1 | P4T-E | Human | Esophagus | ESCC | 1.38e-38 | 9.42e-01 | 0.1323 |
139341 | FUNDC1 | P5T-E | Human | Esophagus | ESCC | 1.25e-15 | 3.15e-01 | 0.1327 |
139341 | FUNDC1 | P8T-E | Human | Esophagus | ESCC | 8.17e-50 | 8.86e-01 | 0.0889 |
139341 | FUNDC1 | P9T-E | Human | Esophagus | ESCC | 2.02e-18 | 2.74e-01 | 0.1131 |
139341 | FUNDC1 | P10T-E | Human | Esophagus | ESCC | 1.68e-17 | 2.98e-01 | 0.116 |
139341 | FUNDC1 | P11T-E | Human | Esophagus | ESCC | 3.96e-15 | 7.19e-01 | 0.1426 |
139341 | FUNDC1 | P12T-E | Human | Esophagus | ESCC | 2.99e-16 | 2.98e-01 | 0.1122 |
139341 | FUNDC1 | P15T-E | Human | Esophagus | ESCC | 2.00e-18 | 3.85e-01 | 0.1149 |
139341 | FUNDC1 | P16T-E | Human | Esophagus | ESCC | 4.40e-25 | 4.99e-01 | 0.1153 |
139341 | FUNDC1 | P17T-E | Human | Esophagus | ESCC | 4.92e-02 | 2.56e-01 | 0.1278 |
139341 | FUNDC1 | P19T-E | Human | Esophagus | ESCC | 2.00e-03 | 2.24e-01 | 0.1662 |
139341 | FUNDC1 | P20T-E | Human | Esophagus | ESCC | 5.92e-15 | 3.90e-01 | 0.1124 |
139341 | FUNDC1 | P21T-E | Human | Esophagus | ESCC | 5.70e-20 | 3.21e-01 | 0.1617 |
139341 | FUNDC1 | P22T-E | Human | Esophagus | ESCC | 3.24e-18 | 2.67e-01 | 0.1236 |
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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:0022411111 | Esophagus | ESCC | cellular component disassembly | 305/8552 | 443/18723 | 1.94e-23 | 4.57e-21 | 305 |
GO:190300816 | Esophagus | ESCC | organelle disassembly | 89/8552 | 114/18723 | 1.36e-12 | 5.80e-11 | 89 |
GO:0070482111 | Esophagus | ESCC | response to oxygen levels | 218/8552 | 347/18723 | 6.91e-11 | 2.17e-09 | 218 |
GO:0036293111 | Esophagus | ESCC | response to decreased oxygen levels | 201/8552 | 322/18723 | 8.37e-10 | 2.04e-08 | 201 |
GO:0001666111 | Esophagus | ESCC | response to hypoxia | 192/8552 | 307/18723 | 1.59e-09 | 3.69e-08 | 192 |
GO:000042217 | Esophagus | ESCC | autophagy of mitochondrion | 63/8552 | 81/18723 | 3.41e-09 | 7.24e-08 | 63 |
GO:006172617 | Esophagus | ESCC | mitochondrion disassembly | 63/8552 | 81/18723 | 3.41e-09 | 7.24e-08 | 63 |
GO:00224117 | Liver | Cirrhotic | cellular component disassembly | 182/4634 | 443/18723 | 1.59e-14 | 1.54e-12 | 182 |
GO:19030084 | Liver | Cirrhotic | organelle disassembly | 59/4634 | 114/18723 | 4.82e-10 | 2.27e-08 | 59 |
GO:00004225 | Liver | Cirrhotic | autophagy of mitochondrion | 43/4634 | 81/18723 | 4.02e-08 | 1.31e-06 | 43 |
GO:00617265 | Liver | Cirrhotic | mitochondrion disassembly | 43/4634 | 81/18723 | 4.02e-08 | 1.31e-06 | 43 |
GO:00704827 | Liver | Cirrhotic | response to oxygen levels | 125/4634 | 347/18723 | 1.55e-06 | 3.02e-05 | 125 |
GO:00362937 | Liver | Cirrhotic | response to decreased oxygen levels | 113/4634 | 322/18723 | 1.87e-05 | 2.52e-04 | 113 |
GO:00016667 | Liver | Cirrhotic | response to hypoxia | 108/4634 | 307/18723 | 2.51e-05 | 3.26e-04 | 108 |
GO:002241112 | Liver | HCC | cellular component disassembly | 282/7958 | 443/18723 | 1.02e-19 | 1.38e-17 | 282 |
GO:190300811 | Liver | HCC | organelle disassembly | 89/7958 | 114/18723 | 8.68e-15 | 5.73e-13 | 89 |
GO:000042211 | Liver | HCC | autophagy of mitochondrion | 64/7958 | 81/18723 | 1.96e-11 | 7.72e-10 | 64 |
GO:006172611 | Liver | HCC | mitochondrion disassembly | 64/7958 | 81/18723 | 1.96e-11 | 7.72e-10 | 64 |
GO:000166612 | Liver | HCC | response to hypoxia | 172/7958 | 307/18723 | 1.06e-06 | 1.59e-05 | 172 |
GO:003629312 | Liver | HCC | response to decreased oxygen levels | 179/7958 | 322/18723 | 1.29e-06 | 1.87e-05 | 179 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa04137210 | Esophagus | ESCC | Mitophagy - animal | 54/4205 | 72/8465 | 9.33e-06 | 4.96e-05 | 2.54e-05 | 54 |
hsa0413738 | Esophagus | ESCC | Mitophagy - animal | 54/4205 | 72/8465 | 9.33e-06 | 4.96e-05 | 2.54e-05 | 54 |
hsa0413721 | Liver | Cirrhotic | Mitophagy - animal | 39/2530 | 72/8465 | 1.38e-05 | 1.24e-04 | 7.64e-05 | 39 |
hsa0413731 | Liver | Cirrhotic | Mitophagy - animal | 39/2530 | 72/8465 | 1.38e-05 | 1.24e-04 | 7.64e-05 | 39 |
hsa0413741 | Liver | HCC | Mitophagy - animal | 53/4020 | 72/8465 | 5.49e-06 | 4.59e-05 | 2.56e-05 | 53 |
hsa0413751 | Liver | HCC | Mitophagy - animal | 53/4020 | 72/8465 | 5.49e-06 | 4.59e-05 | 2.56e-05 | 53 |
hsa0413728 | Oral cavity | OSCC | Mitophagy - animal | 58/3704 | 72/8465 | 1.48e-10 | 2.07e-09 | 1.05e-09 | 58 |
hsa04137112 | Oral cavity | OSCC | Mitophagy - animal | 58/3704 | 72/8465 | 1.48e-10 | 2.07e-09 | 1.05e-09 | 58 |
hsa0413729 | Oral cavity | LP | Mitophagy - animal | 38/2418 | 72/8465 | 1.24e-05 | 8.63e-05 | 5.57e-05 | 38 |
hsa0413737 | Oral cavity | LP | Mitophagy - animal | 38/2418 | 72/8465 | 1.24e-05 | 8.63e-05 | 5.57e-05 | 38 |
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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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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 |
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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 |
FUNDC1 | SNV | Missense_Mutation | novel | c.349N>T | p.Ala117Ser | p.A117S | Q8IVP5 | protein_coding | tolerated(0.56) | benign(0.076) | TCGA-A2-A4S1-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FUNDC1 | insertion | In_Frame_Ins | novel | c.71_72insGAAGGA | p.Thr24_Glu25insLysAsp | p.T24_E25insKD | Q8IVP5 | protein_coding | TCGA-A7-A26I-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | cytoxan | SD | ||
FUNDC1 | SNV | Missense_Mutation | c.110N>G | p.Phe37Cys | p.F37C | Q8IVP5 | protein_coding | deleterious(0) | possibly_damaging(0.862) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
FUNDC1 | SNV | Missense_Mutation | c.322N>G | p.Lys108Glu | p.K108E | Q8IVP5 | protein_coding | deleterious(0.03) | possibly_damaging(0.766) | TCGA-AA-A02Y-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
FUNDC1 | SNV | Missense_Mutation | rs777393435 | c.31N>G | p.Tyr11Asp | p.Y11D | Q8IVP5 | protein_coding | tolerated(0.17) | benign(0.026) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
FUNDC1 | SNV | Missense_Mutation | novel | c.191N>T | p.Ala64Val | p.A64V | Q8IVP5 | protein_coding | tolerated(0.31) | benign(0.133) | TCGA-AX-A0J1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FUNDC1 | SNV | Missense_Mutation | rs181489310 | c.46G>A | p.Asp16Asn | p.D16N | Q8IVP5 | protein_coding | tolerated(0.24) | benign(0.005) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
FUNDC1 | SNV | Missense_Mutation | c.313N>T | p.Asp105Tyr | p.D105Y | Q8IVP5 | protein_coding | deleterious(0.02) | probably_damaging(0.983) | TCGA-BS-A0TC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
FUNDC1 | SNV | Missense_Mutation | novel | c.385N>A | p.Glu129Lys | p.E129K | Q8IVP5 | protein_coding | tolerated(0.08) | benign(0.081) | TCGA-BS-A0UF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FUNDC1 | SNV | Missense_Mutation | novel | c.71C>A | p.Thr24Asn | p.T24N | Q8IVP5 | protein_coding | deleterious(0) | possibly_damaging(0.674) | TCGA-D1-A102-01 | Endometrium | uterine corpus endometrioid carcinoma | 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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