EOLA2 endothelium and lymphocyte associated ASCH domain 2
Information
- Symbol
- EOLA2
- Type
- protein-coding
- Description
- endothelium and lymphocyte associated ASCH domain 2
- Entrez Gene ID
- 541578
- Genome
- hg19
- Position
- chrX:149,100,415-149,106,709
- Genome
- hg38
- Position
- chrX:149,932,197-149,938,491
- HGNC
- HGNC:17402 HGNC
- Ensembl
- ENSG00000197021 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 10 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
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MGeND data only
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| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CXorf40B |
| HGNC | HGNC:17402 HGNC |
| Ensembl | ENSG00000197021 Ensembl |
| AllianceGenome | HGNC:17402 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000462691.5 | hg38 | chrX | 149,929,527 | 149,938,435 | 8,909 |
| ENST00000370404.5 | hg38 | chrX | 149,932,201 | 149,938,459 | 6,259 |
| ENST00000370406.8 | hg38 | chrX | 149,932,197 | 149,938,491 | 6,295 |
| ENST00000355203.6 | hg38 | chrX | 149,932,198 | 149,937,514 | 5,317 |
| ENST00000462691.5 | hg19 | chrX | 149,097,745 | 149,106,653 | 8,909 |
| ENST00000370406.8 | hg19 | chrX | 149,100,415 | 149,106,709 | 6,295 |
| ENST00000355203.6 | hg19 | chrX | 149,100,416 | 149,105,732 | 5,317 |
| ENST00000370404.5 | hg19 | chrX | 149,100,419 | 149,106,677 | 6,259 |
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