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Gene: LHX9 |
Gene summary for LHX9 |
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Gene information | Species | Human | Gene symbol | LHX9 | Gene ID | 56956 |
Gene name | LIM homeobox 9 | |
Gene Alias | LHX9 | |
Cytomap | 1q31.3 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | Q9NQ69 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
56956 | LHX9 | ATC13 | Human | Thyroid | ATC | 2.18e-22 | 5.44e-01 | 0.34 |
56956 | LHX9 | ATC5 | Human | Thyroid | ATC | 9.23e-23 | 5.69e-01 | 0.34 |
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Tissue | Expression Dynamics | Abbreviation |
Thyroid | ![]() | ATC: Anaplastic thyroid cancer |
HT: Hashimoto's thyroiditis | ||
PTC: Papillary thyroid cancer |
∗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:006156423 | Thyroid | ATC | axon development | 220/6293 | 467/18723 | 6.85e-10 | 1.80e-08 | 220 |
GO:000740919 | Thyroid | ATC | axonogenesis | 197/6293 | 418/18723 | 5.09e-09 | 1.13e-07 | 197 |
GO:006145827 | Thyroid | ATC | reproductive system development | 193/6293 | 427/18723 | 3.32e-07 | 4.92e-06 | 193 |
GO:004860825 | Thyroid | ATC | reproductive structure development | 190/6293 | 424/18723 | 8.40e-07 | 1.11e-05 | 190 |
GO:004654621 | Thyroid | ATC | development of primary male sexual characteristics | 72/6293 | 142/18723 | 1.85e-05 | 1.69e-04 | 72 |
GO:000858421 | Thyroid | ATC | male gonad development | 71/6293 | 141/18723 | 2.83e-05 | 2.38e-04 | 71 |
GO:004666112 | Thyroid | ATC | male sex differentiation | 77/6293 | 165/18723 | 3.27e-04 | 2.04e-03 | 77 |
GO:000840613 | Thyroid | ATC | gonad development | 96/6293 | 221/18723 | 1.40e-03 | 7.25e-03 | 96 |
GO:00451374 | Thyroid | ATC | development of primary sexual characteristics | 97/6293 | 227/18723 | 2.47e-03 | 1.14e-02 | 97 |
GO:00074113 | Thyroid | ATC | axon guidance | 96/6293 | 227/18723 | 3.74e-03 | 1.63e-02 | 96 |
GO:00974853 | Thyroid | ATC | neuron projection guidance | 96/6293 | 228/18723 | 4.36e-03 | 1.81e-02 | 96 |
GO:00466603 | Thyroid | ATC | female sex differentiation | 51/6293 | 114/18723 | 8.62e-03 | 3.28e-02 | 51 |
GO:00085853 | Thyroid | ATC | female gonad development | 43/6293 | 95/18723 | 1.19e-02 | 4.22e-02 | 43 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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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 |
LHX9 | CLUB | Lung | IAC | HMGN3,PIGR,MAP1B, etc. | 2.54e-01 | ![]() |
LHX9 | iATC | Thyroid | PTC | NPPC,CHODL,PTPRT, etc. | 1.46e-02 | ![]() |
∗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 |
LHX9 | SNV | Missense_Mutation | c.805N>A | p.Arg269Ser | p.R269S | Q9NQ69 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-XK-AAIR-01 | Prostate | prostate adenocarcinoma | Male | >=65 | 8 | Unknown | Unknown | SD | |
LHX9 | SNV | Missense_Mutation | c.442N>T | p.Arg148Cys | p.R148C | Q9NQ69 | protein_coding | deleterious(0.02) | benign(0.219) | TCGA-BR-4371-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
LHX9 | SNV | Missense_Mutation | c.1108N>G | p.Ile370Val | p.I370V | Q9NQ69 | protein_coding | tolerated(0.28) | benign(0) | TCGA-BR-8295-01 | Stomach | stomach adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
LHX9 | SNV | Missense_Mutation | c.650N>C | p.Asn217Thr | p.N217T | Q9NQ69 | protein_coding | tolerated(0.11) | benign(0.206) | TCGA-BR-8589-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD | |
LHX9 | SNV | Missense_Mutation | c.812N>A | p.Arg271Gln | p.R271Q | Q9NQ69 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BR-8680-01 | Stomach | stomach adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | CR | |
LHX9 | SNV | Missense_Mutation | c.1075G>A | p.Ala359Thr | p.A359T | Q9NQ69 | protein_coding | tolerated(0.18) | benign(0.001) | TCGA-HU-A4GN-01 | Stomach | stomach adenocarcinoma | Male | <65 | I/II | Chemotherapy | mitomycin | PD | |
LHX9 | SNV | Missense_Mutation | novel | c.846N>A | p.Met282Ile | p.M282I | Q9NQ69 | protein_coding | deleterious(0) | possibly_damaging(0.734) | TCGA-IN-A6RJ-01 | Stomach | stomach adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
LHX9 | SNV | Missense_Mutation | novel | c.1016N>A | p.Gly339Asp | p.G339D | Q9NQ69 | protein_coding | tolerated(0.55) | benign(0.005) | TCGA-VQ-A8P2-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unspecific | Complete Response |
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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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