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Gene: ORAI1 |
Gene summary for ORAI1 |
Gene summary. |
Gene information | Species | Human | Gene symbol | ORAI1 | Gene ID | 84876 |
Gene name | ORAI calcium release-activated calcium modulator 1 | |
Gene Alias | CRACM1 | |
Cytomap | 12q24.31 | |
Gene Type | protein-coding | GO ID | GO:0002115 | UniProtAcc | A0A024RBT3 |
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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 |
84876 | ORAI1 | P48T-E | Human | Esophagus | ESCC | 2.39e-07 | 1.26e-01 | 0.0959 |
84876 | ORAI1 | P49T-E | Human | Esophagus | ESCC | 2.64e-10 | 6.37e-01 | 0.1768 |
84876 | ORAI1 | P52T-E | Human | Esophagus | ESCC | 4.28e-22 | 3.95e-01 | 0.1555 |
84876 | ORAI1 | P54T-E | Human | Esophagus | ESCC | 1.89e-11 | 2.38e-01 | 0.0975 |
84876 | ORAI1 | P56T-E | Human | Esophagus | ESCC | 3.18e-03 | 4.94e-01 | 0.1613 |
84876 | ORAI1 | P57T-E | Human | Esophagus | ESCC | 8.48e-05 | 1.09e-01 | 0.0926 |
84876 | ORAI1 | P62T-E | Human | Esophagus | ESCC | 6.31e-10 | 2.02e-01 | 0.1302 |
84876 | ORAI1 | P65T-E | Human | Esophagus | ESCC | 8.17e-14 | 2.95e-01 | 0.0978 |
84876 | ORAI1 | P74T-E | Human | Esophagus | ESCC | 3.62e-04 | 1.73e-01 | 0.1479 |
84876 | ORAI1 | P75T-E | Human | Esophagus | ESCC | 1.70e-15 | 2.20e-01 | 0.1125 |
84876 | ORAI1 | P76T-E | Human | Esophagus | ESCC | 4.79e-12 | 2.23e-01 | 0.1207 |
84876 | ORAI1 | P79T-E | Human | Esophagus | ESCC | 5.80e-05 | 5.65e-02 | 0.1154 |
84876 | ORAI1 | P80T-E | Human | Esophagus | ESCC | 5.23e-06 | 2.14e-01 | 0.155 |
84876 | ORAI1 | P83T-E | Human | Esophagus | ESCC | 2.14e-12 | 4.30e-01 | 0.1738 |
84876 | ORAI1 | P89T-E | Human | Esophagus | ESCC | 2.69e-04 | 3.33e-01 | 0.1752 |
84876 | ORAI1 | P91T-E | Human | Esophagus | ESCC | 3.36e-05 | 4.05e-01 | 0.1828 |
84876 | ORAI1 | P107T-E | Human | Esophagus | ESCC | 2.99e-12 | 2.53e-01 | 0.171 |
84876 | ORAI1 | P127T-E | Human | Esophagus | ESCC | 3.06e-03 | 8.91e-02 | 0.0826 |
84876 | ORAI1 | P128T-E | Human | Esophagus | ESCC | 1.29e-11 | 3.56e-01 | 0.1241 |
84876 | ORAI1 | P130T-E | Human | Esophagus | ESCC | 4.04e-50 | 8.77e-01 | 0.1676 |
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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:0048732 | Colorectum | AD | gland development | 149/3918 | 436/18723 | 6.07e-11 | 6.33e-09 | 149 |
GO:0030879 | Colorectum | AD | mammary gland development | 53/3918 | 137/18723 | 1.46e-06 | 4.58e-05 | 53 |
GO:0061180 | Colorectum | AD | mammary gland epithelium development | 28/3918 | 67/18723 | 8.74e-05 | 1.35e-03 | 28 |
GO:00487321 | Colorectum | SER | gland development | 112/2897 | 436/18723 | 1.75e-08 | 1.28e-06 | 112 |
GO:00611801 | Colorectum | SER | mammary gland epithelium development | 22/2897 | 67/18723 | 3.11e-04 | 5.03e-03 | 22 |
GO:00308791 | Colorectum | SER | mammary gland development | 37/2897 | 137/18723 | 3.61e-04 | 5.61e-03 | 37 |
GO:00487322 | Colorectum | MSS | gland development | 143/3467 | 436/18723 | 3.85e-13 | 8.01e-11 | 143 |
GO:00308792 | Colorectum | MSS | mammary gland development | 51/3467 | 137/18723 | 1.88e-07 | 8.26e-06 | 51 |
GO:00611802 | Colorectum | MSS | mammary gland epithelium development | 28/3467 | 67/18723 | 8.47e-06 | 2.11e-04 | 28 |
GO:0051349 | Colorectum | MSS | positive regulation of lyase activity | 10/3467 | 23/18723 | 5.06e-03 | 3.47e-02 | 10 |
GO:00487323 | Colorectum | MSI-H | gland development | 53/1319 | 436/18723 | 7.08e-05 | 2.35e-03 | 53 |
GO:0048732111 | Esophagus | ESCC | gland development | 269/8552 | 436/18723 | 7.81e-12 | 2.95e-10 | 269 |
GO:003087914 | Esophagus | ESCC | mammary gland development | 85/8552 | 137/18723 | 8.11e-05 | 6.01e-04 | 85 |
GO:00611807 | Esophagus | ESCC | mammary gland epithelium development | 43/8552 | 67/18723 | 1.73e-03 | 7.97e-03 | 43 |
GO:004873222 | Liver | HCC | gland development | 242/7958 | 436/18723 | 2.26e-08 | 5.28e-07 | 242 |
GO:00308795 | Liver | HCC | mammary gland development | 75/7958 | 137/18723 | 2.52e-03 | 1.22e-02 | 75 |
GO:004873220 | Oral cavity | OSCC | gland development | 226/7305 | 436/18723 | 2.78e-08 | 5.39e-07 | 226 |
GO:003087910 | Oral cavity | OSCC | mammary gland development | 69/7305 | 137/18723 | 4.43e-03 | 1.79e-02 | 69 |
GO:0048732110 | Oral cavity | LP | gland development | 149/4623 | 436/18723 | 4.51e-06 | 9.17e-05 | 149 |
GO:004873227 | Skin | cSCC | gland development | 167/4864 | 436/18723 | 7.64e-09 | 2.44e-07 | 167 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa046112 | Liver | HCC | Platelet activation | 71/4020 | 124/8465 | 1.77e-02 | 4.15e-02 | 2.31e-02 | 71 |
hsa0461111 | Liver | HCC | Platelet activation | 71/4020 | 124/8465 | 1.77e-02 | 4.15e-02 | 2.31e-02 | 71 |
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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 |
ORAI1 | SNV | Missense_Mutation | novel | c.709N>C | p.Tyr237His | p.Y237H | protein_coding | deleterious_low_confidence(0) | benign(0.185) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD | |
ORAI1 | deletion | Frame_Shift_Del | novel | c.672delN | p.His225ThrfsTer7 | p.H225Tfs*7 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD | |||
ORAI1 | SNV | Missense_Mutation | rs782280709 | c.251A>G | p.Asn84Ser | p.N84S | protein_coding | deleterious(0.03) | probably_damaging(0.926) | TCGA-ZJ-AAX4-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
ORAI1 | SNV | Missense_Mutation | novel | c.614G>A | p.Arg205Gln | p.R205Q | protein_coding | tolerated(0.08) | probably_damaging(0.978) | TCGA-A6-2679-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ORAI1 | SNV | Missense_Mutation | novel | c.427N>T | p.Pro143Ser | p.P143S | protein_coding | tolerated_low_confidence(0.77) | benign(0.003) | TCGA-A6-2686-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ORAI1 | SNV | Missense_Mutation | rs782538669 | c.310N>T | p.Arg104Cys | p.R104C | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A6-A565-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unspecific | 5FU | PD | |
ORAI1 | SNV | Missense_Mutation | rs368310115 | c.221N>T | p.Ala74Val | p.A74V | protein_coding | deleterious(0) | possibly_damaging(0.869) | TCGA-AA-3821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
ORAI1 | SNV | Missense_Mutation | novel | c.481N>A | p.Val161Ile | p.V161I | protein_coding | tolerated(0.27) | benign(0.017) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
ORAI1 | SNV | Missense_Mutation | novel | c.636N>T | p.Glu212Asp | p.E212D | protein_coding | tolerated(0.07) | probably_damaging(0.978) | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ORAI1 | SNV | Missense_Mutation | novel | c.686A>C | p.His229Pro | p.H229P | protein_coding | tolerated(0.25) | benign(0) | TCGA-A5-A0GP-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | 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 |
84876 | ORAI1 | TRANSCRIPTION FACTOR, ION CHANNEL, TRANSPORTER | CM2489 | |||
84876 | ORAI1 | TRANSCRIPTION FACTOR, ION CHANNEL, TRANSPORTER | blocker | 381118797 | ||
84876 | ORAI1 | TRANSCRIPTION FACTOR, ION CHANNEL, TRANSPORTER | blocker | 381118798 | ||
84876 | ORAI1 | TRANSCRIPTION FACTOR, ION CHANNEL, TRANSPORTER | RP4010 | |||
84876 | ORAI1 | TRANSCRIPTION FACTOR, ION CHANNEL, TRANSPORTER | blocker | 375973230 | ||
84876 | ORAI1 | TRANSCRIPTION FACTOR, ION CHANNEL, TRANSPORTER | blocker | 375973229 |
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