chrX:73820651:> Detail (hg38)
Information
Genome
| Assembly | Position |
|---|---|
| hg19 | chrX:73,040,486-73,072,558 |
| hg38 | chrX:73,820,651-73,852,723 |
HGVS
| Type | Transcript | Protein |
|---|---|---|
Summary
MGeND
| Clinical significance | |
| Variant entry | |
| GWAS entry | |
| Disease area statistics | Show details |
Frequency
[No Data.]
Prediction
[No Data.]
ClinVar
| Clinical Significance | |
| Review star | [No Data.] |
| Show details | |
Links
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
[No Data.]
CIViC
[No Data.]
DisGeNET
| Score | Disease name | Description | Source | Pubmed | Links |
|---|---|---|---|---|---|
| <0.001 | Congenital chromosomal disease | The aim of the present study was to propose a feasible and practical molecular d... | BeFree | 25535777 | Detail |
| <0.001 | Dwarfism | NA | BeFree | Detail | |
| <0.001 | glioblastoma | Knockdown of long non-coding RNA XIST exerts tumor-suppressive functions in huma... | BeFree | 25578780 | Detail |
| <0.001 | Glioma | Taken together, these results provided a comprehensive analysis of XIST in GSCs ... | BeFree | 25578780 | Detail |
| 0.120 | influenza | NA | CTD_human | Detail | |
| <0.001 | Fibroid Tumor | NA | BeFree | Detail | |
| <0.001 | leukemia | NA | BeFree | Detail | |
| 0.001 | Mental Retardation | NA | BeFree | Detail | |
| <0.001 | Myelodysplasia | NA | BeFree | Detail | |
| <0.001 | Neoplasm Metastasis | In this study, a review of the literature found that lncRNAs H19, LSINCT5, and X... | BeFree | 25756403 | Detail |
| <0.001 | oligospermia | NA | BeFree | Detail | |
| <0.001 | ovarian carcinoma | In this study, a review of the literature found that lncRNAs H19, LSINCT5, and X... | BeFree | 25756403 | Detail |
| <0.001 | Parkinson disease | Among 10 distinct genes which are identified in PD patients' samples, DLG1, XIST... | BeFree | 25275262 | Detail |
| <0.001 | Preleukemia | NA | BeFree | Detail | |
| <0.001 | seminoma | NA | BeFree | Detail | |
| <0.001 | Severe mental retardation (I.Q. 20-34) | NA | BeFree | Detail | |
| <0.001 | Testicular Neoplasms | NA | BeFree | Detail | |
| <0.001 | Uterine Fibroids | NA | BeFree | Detail | |
| <0.001 | Germ cell tumor | NA | BeFree | Detail | |
| <0.001 | embryonal carcinoma | NA | BeFree | Detail | |
| <0.001 | Superficial ulcer | NA | BeFree | Detail | |
| <0.001 | Triploidy syndrome | NA | BeFree | Detail | |
| <0.001 | Developmental delay (disorder) | NA | BeFree | Detail | |
| <0.001 | XX males | NA | BeFree | Detail | |
| <0.001 | Epithelial ovarian cancer | NA | BeFree | Detail | |
| <0.001 | breast carcinoma | NA | BeFree | Detail | |
| <0.001 | Kabuki make-up syndrome | NA | BeFree | Detail | |
| <0.001 | Malignant neoplasm of ovary | In this study, a review of the literature found that lncRNAs H19, LSINCT5, and X... | BeFree | 25756403 | Detail |
| <0.001 | Single tumor | NA | BeFree | Detail | |
| <0.001 | Congenital malformation syndrome | NA | BeFree | Detail | |
| <0.001 | Testicular Germ Cell Tumor | NA | BeFree | Detail | |
| 0.120 | X INACTIVATION, FAMILIAL SKEWED, 1 (disorder) | NA | CLINVAR | Detail | |
| <0.001 | Congenital Abnormality | NA | BeFree | Detail | |
| <0.001 | Malignant neoplasm of breast | NA | BeFree | Detail |
Annotation
Annotations
| Descrption | Source | Links |
|---|---|---|
| The aim of the present study was to propose a feasible and practical molecular diagnostic tool for n... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| Knockdown of long non-coding RNA XIST exerts tumor-suppressive functions in human glioblastoma stem ... | DisGeNET | Detail |
| Taken together, these results provided a comprehensive analysis of XIST in GSCs and important clues ... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| In this study, a review of the literature found that lncRNAs H19, LSINCT5, and XIST have a close rel... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| In this study, a review of the literature found that lncRNAs H19, LSINCT5, and XIST have a close rel... | DisGeNET | Detail |
| Among 10 distinct genes which are identified in PD patients' samples, DLG1, XIST, DDX3Y and RPS4Y1 g... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| In this study, a review of the literature found that lncRNAs H19, LSINCT5, and XIST have a close rel... | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
| NA | DisGeNET | Detail |
Overlapped Transcript Coordinates
| Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
|---|
Overlapped Transcript
| Gene | Transcript ID | Chromosome | Start | Stop | Links |
|---|
- Gene
- -
- Genome
- hg38
- Position
- chrX:73,820,651-73,852,723
- Variant Type
- snv
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