PXN-AS1 PXN antisense RNA 1
Information
- Symbol
- PXN-AS1
- Type
- ncRNA
- Description
- PXN antisense RNA 1
- Entrez Gene ID
- 100506649
- Genome
- hg19
- Position
- chr12:120,639,159-120,651,013
- Genome
- hg38
- Position
- chr12:120,201,356-120,213,210
- HGNC
- HGNC:44123 HGNC
- Ensembl
- ENSG00000255857 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
0 |
 |
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
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| 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 | EyeLinc4 |
| HGNC | HGNC:44123 HGNC |
| Ensembl | ENSG00000255857 Ensembl |
| AllianceGenome | HGNC:44123 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000693713.1 | hg38 | chr12 | 120,201,354 | 120,212,769 | 11,416 |
| ENST00000535200.2 | hg38 | chr12 | 120,201,342 | 120,213,138 | 11,797 |
| ENST00000539446.6 | hg38 | chr12 | 120,201,372 | 120,211,859 | 10,488 |
| ENST00000664264.1 | hg38 | chr12 | 120,201,325 | 120,208,054 | 6,730 |
| ENST00000667017.1 | hg38 | chr12 | 120,201,356 | 120,213,210 | 11,855 |
| ENST00000664264.1 | hg19 | chr12 | 120,639,128 | 120,645,857 | 6,730 |
| ENST00000535200.2 | hg19 | chr12 | 120,639,145 | 120,650,941 | 11,797 |
| ENST00000693713.1 | hg19 | chr12 | 120,639,157 | 120,650,572 | 11,416 |
| ENST00000667017.1 | hg19 | chr12 | 120,639,159 | 120,651,013 | 11,855 |
| ENST00000539446.6 | hg19 | chr12 | 120,639,175 | 120,649,662 | 10,488 |
Genome browser