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Gene: ANAPC2 |
Gene summary for ANAPC2 |
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Gene information | Species | Human | Gene symbol | ANAPC2 | Gene ID | 29882 |
Gene name | anaphase promoting complex subunit 2 | |
Gene Alias | APC2 | |
Cytomap | 9q34.3 | |
Gene Type | protein-coding | GO ID | GO:0000209 | UniProtAcc | Q9UJX6 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
29882 | ANAPC2 | P54T-E | Human | Esophagus | ESCC | 1.02e-12 | 2.11e-01 | 0.0975 |
29882 | ANAPC2 | P56T-E | Human | Esophagus | ESCC | 1.07e-04 | 3.83e-01 | 0.1613 |
29882 | ANAPC2 | P57T-E | Human | Esophagus | ESCC | 1.67e-17 | 1.97e-01 | 0.0926 |
29882 | ANAPC2 | P61T-E | Human | Esophagus | ESCC | 3.50e-13 | 3.30e-01 | 0.099 |
29882 | ANAPC2 | P62T-E | Human | Esophagus | ESCC | 3.06e-20 | 3.58e-01 | 0.1302 |
29882 | ANAPC2 | P65T-E | Human | Esophagus | ESCC | 2.99e-09 | 2.04e-01 | 0.0978 |
29882 | ANAPC2 | P74T-E | Human | Esophagus | ESCC | 7.31e-33 | 9.40e-01 | 0.1479 |
29882 | ANAPC2 | P75T-E | Human | Esophagus | ESCC | 1.24e-32 | 5.66e-01 | 0.1125 |
29882 | ANAPC2 | P76T-E | Human | Esophagus | ESCC | 1.84e-17 | 2.63e-01 | 0.1207 |
29882 | ANAPC2 | P79T-E | Human | Esophagus | ESCC | 6.86e-15 | 1.99e-01 | 0.1154 |
29882 | ANAPC2 | P80T-E | Human | Esophagus | ESCC | 1.32e-22 | 6.34e-01 | 0.155 |
29882 | ANAPC2 | P82T-E | Human | Esophagus | ESCC | 6.53e-11 | 5.75e-01 | 0.1072 |
29882 | ANAPC2 | P83T-E | Human | Esophagus | ESCC | 7.82e-15 | 3.86e-01 | 0.1738 |
29882 | ANAPC2 | P84T-E | Human | Esophagus | ESCC | 3.41e-13 | 4.03e-01 | 0.0933 |
29882 | ANAPC2 | P89T-E | Human | Esophagus | ESCC | 1.57e-06 | 4.49e-01 | 0.1752 |
29882 | ANAPC2 | P91T-E | Human | Esophagus | ESCC | 3.14e-12 | 1.27e+00 | 0.1828 |
29882 | ANAPC2 | P94T-E | Human | Esophagus | ESCC | 1.05e-03 | 3.16e-01 | 0.0879 |
29882 | ANAPC2 | P104T-E | Human | Esophagus | ESCC | 1.94e-03 | 3.38e-01 | 0.0931 |
29882 | ANAPC2 | P107T-E | Human | Esophagus | ESCC | 1.61e-34 | 7.37e-01 | 0.171 |
29882 | ANAPC2 | P126T-E | Human | Esophagus | ESCC | 1.09e-04 | 6.03e-01 | 0.1125 |
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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:000020917 | Esophagus | ESCC | protein polyubiquitination | 170/8552 | 236/18723 | 1.40e-16 | 1.09e-14 | 170 |
GO:0016049110 | Esophagus | ESCC | cell growth | 289/8552 | 482/18723 | 1.29e-10 | 3.77e-09 | 289 |
GO:000155819 | Esophagus | ESCC | regulation of cell growth | 248/8552 | 414/18723 | 2.97e-09 | 6.45e-08 | 248 |
GO:003253520 | Esophagus | ESCC | regulation of cellular component size | 227/8552 | 383/18723 | 4.77e-08 | 8.60e-07 | 227 |
GO:007097912 | Esophagus | ESCC | protein K11-linked ubiquitination | 27/8552 | 29/18723 | 8.09e-08 | 1.39e-06 | 27 |
GO:002260420 | Esophagus | ESCC | regulation of cell morphogenesis | 180/8552 | 309/18723 | 5.19e-06 | 5.45e-05 | 180 |
GO:003134616 | Esophagus | ESCC | positive regulation of cell projection organization | 201/8552 | 353/18723 | 1.19e-05 | 1.11e-04 | 201 |
GO:001072010 | Esophagus | ESCC | positive regulation of cell development | 172/8552 | 298/18723 | 1.74e-05 | 1.55e-04 | 172 |
GO:005076710 | Esophagus | ESCC | regulation of neurogenesis | 203/8552 | 364/18723 | 6.10e-05 | 4.68e-04 | 203 |
GO:00507697 | Esophagus | ESCC | positive regulation of neurogenesis | 131/8552 | 225/18723 | 9.71e-05 | 6.90e-04 | 131 |
GO:003030710 | Esophagus | ESCC | positive regulation of cell growth | 100/8552 | 166/18723 | 1.07e-04 | 7.55e-04 | 100 |
GO:00083619 | Esophagus | ESCC | regulation of cell size | 107/8552 | 181/18723 | 1.81e-04 | 1.16e-03 | 107 |
GO:006156415 | Esophagus | ESCC | axon development | 251/8552 | 467/18723 | 2.41e-04 | 1.49e-03 | 251 |
GO:001097516 | Esophagus | ESCC | regulation of neuron projection development | 240/8552 | 445/18723 | 2.48e-04 | 1.53e-03 | 240 |
GO:001076920 | Esophagus | ESCC | regulation of cell morphogenesis involved in differentiation | 61/8552 | 96/18723 | 3.12e-04 | 1.85e-03 | 61 |
GO:00519606 | Esophagus | ESCC | regulation of nervous system development | 237/8552 | 443/18723 | 5.02e-04 | 2.78e-03 | 237 |
GO:001077018 | Esophagus | ESCC | positive regulation of cell morphogenesis involved in differentiation | 51/8552 | 79/18723 | 5.48e-04 | 3.00e-03 | 51 |
GO:006056010 | Esophagus | ESCC | developmental growth involved in morphogenesis | 131/8552 | 234/18723 | 9.28e-04 | 4.73e-03 | 131 |
GO:00519625 | Esophagus | ESCC | positive regulation of nervous system development | 149/8552 | 272/18723 | 1.50e-03 | 7.06e-03 | 149 |
GO:00457738 | Esophagus | ESCC | positive regulation of axon extension | 29/8552 | 42/18723 | 1.87e-03 | 8.46e-03 | 29 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0412027 | Esophagus | ESCC | Ubiquitin mediated proteolysis | 122/4205 | 142/8465 | 6.53e-20 | 7.29e-18 | 3.74e-18 | 122 |
hsa0411023 | Esophagus | ESCC | Cell cycle | 126/4205 | 157/8465 | 1.34e-15 | 5.60e-14 | 2.87e-14 | 126 |
hsa05166211 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
hsa041146 | Esophagus | ESCC | Oocyte meiosis | 77/4205 | 131/8465 | 2.19e-02 | 4.80e-02 | 2.46e-02 | 77 |
hsa0412036 | Esophagus | ESCC | Ubiquitin mediated proteolysis | 122/4205 | 142/8465 | 6.53e-20 | 7.29e-18 | 3.74e-18 | 122 |
hsa0411033 | Esophagus | ESCC | Cell cycle | 126/4205 | 157/8465 | 1.34e-15 | 5.60e-14 | 2.87e-14 | 126 |
hsa05166310 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
hsa0411411 | Esophagus | ESCC | Oocyte meiosis | 77/4205 | 131/8465 | 2.19e-02 | 4.80e-02 | 2.46e-02 | 77 |
hsa0412021 | Liver | Cirrhotic | Ubiquitin mediated proteolysis | 72/2530 | 142/8465 | 1.32e-07 | 1.97e-06 | 1.21e-06 | 72 |
hsa0516614 | Liver | Cirrhotic | Human T-cell leukemia virus 1 infection | 87/2530 | 222/8465 | 1.69e-03 | 8.01e-03 | 4.94e-03 | 87 |
hsa041104 | Liver | Cirrhotic | Cell cycle | 61/2530 | 157/8465 | 9.53e-03 | 3.21e-02 | 1.98e-02 | 61 |
hsa0412031 | Liver | Cirrhotic | Ubiquitin mediated proteolysis | 72/2530 | 142/8465 | 1.32e-07 | 1.97e-06 | 1.21e-06 | 72 |
hsa0516615 | Liver | Cirrhotic | Human T-cell leukemia virus 1 infection | 87/2530 | 222/8465 | 1.69e-03 | 8.01e-03 | 4.94e-03 | 87 |
hsa0411011 | Liver | Cirrhotic | Cell cycle | 61/2530 | 157/8465 | 9.53e-03 | 3.21e-02 | 1.98e-02 | 61 |
hsa0412041 | Liver | HCC | Ubiquitin mediated proteolysis | 110/4020 | 142/8465 | 1.67e-13 | 3.74e-12 | 2.08e-12 | 110 |
hsa041102 | Liver | HCC | Cell cycle | 106/4020 | 157/8465 | 2.54e-07 | 3.04e-06 | 1.69e-06 | 106 |
hsa0516622 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
hsa0412051 | Liver | HCC | Ubiquitin mediated proteolysis | 110/4020 | 142/8465 | 1.67e-13 | 3.74e-12 | 2.08e-12 | 110 |
hsa041103 | Liver | HCC | Cell cycle | 106/4020 | 157/8465 | 2.54e-07 | 3.04e-06 | 1.69e-06 | 106 |
hsa0516632 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
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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 |
ANAPC2 | SNV | Missense_Mutation | novel | c.507N>A | p.Phe169Leu | p.F169L | Q9UJX6 | protein_coding | tolerated(0.44) | benign(0.07) | TCGA-DG-A2KK-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
ANAPC2 | SNV | Missense_Mutation | rs878889078 | c.167N>A | p.Arg56Gln | p.R56Q | Q9UJX6 | protein_coding | tolerated(0.51) | benign(0) | TCGA-EA-A5FO-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
ANAPC2 | SNV | Missense_Mutation | novel | c.516G>A | p.Met172Ile | p.M172I | Q9UJX6 | protein_coding | tolerated(1) | benign(0.007) | TCGA-EX-A8YF-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD |
ANAPC2 | SNV | Missense_Mutation | c.500N>A | p.Arg167Lys | p.R167K | Q9UJX6 | protein_coding | tolerated(0.93) | benign(0) | TCGA-IR-A3LH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
ANAPC2 | SNV | Missense_Mutation | c.486C>G | p.Phe162Leu | p.F162L | Q9UJX6 | protein_coding | tolerated(0.75) | benign(0.003) | TCGA-LP-A5U2-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unknown | Unknown | SD | |
ANAPC2 | SNV | Missense_Mutation | c.2380G>A | p.Glu794Lys | p.E794K | Q9UJX6 | protein_coding | deleterious(0) | probably_damaging(0.986) | TCGA-LP-A7HU-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
ANAPC2 | SNV | Missense_Mutation | c.244N>A | p.Asp82Asn | p.D82N | Q9UJX6 | protein_coding | tolerated(0.29) | possibly_damaging(0.462) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
ANAPC2 | SNV | Missense_Mutation | rs768895745 | c.1487N>A | p.Arg496Gln | p.R496Q | Q9UJX6 | protein_coding | tolerated(0.08) | possibly_damaging(0.64) | TCGA-AA-A03F-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
ANAPC2 | SNV | Missense_Mutation | c.1445N>T | p.Pro482Leu | p.P482L | Q9UJX6 | protein_coding | deleterious(0.03) | probably_damaging(1) | TCGA-AY-6197-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
ANAPC2 | SNV | Missense_Mutation | c.1222N>A | p.Arg408Ser | p.R408S | Q9UJX6 | protein_coding | deleterious(0) | probably_damaging(0.925) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <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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