ITGA6-AS1 ITGA6 antisense RNA 1
Information
- Symbol
- ITGA6-AS1
- Type
- ncRNA
- Description
- ITGA6 antisense RNA 1
- Entrez Gene ID
- 101929947
- Genome
- hg19
- Position
- chr2:173,368,167-173,421,324
- Genome
- hg38
- Position
- chr2:172,503,439-172,556,596
- HGNC
- HGNC:40308 HGNC
- Ensembl
- ENSG00000232788 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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000442417.5 | hg38 | chr2 | 172,480,840 | 172,556,529 | 75,690 |
ENST00000417539.1 | hg38 | chr2 | 172,465,147 | 172,466,012 | 866 |
ENST00000450443.1 | hg38 | chr2 | 172,503,439 | 172,556,596 | 53,158 |
ENST00000416080.1 | hg38 | chr2 | 172,509,029 | 172,512,510 | 3,482 |
ENST00000715602.1 | hg38 | chr2 | 172,464,262 | 172,552,809 | 88,548 |
ENST00000715602.1 | hg19 | chr2 | 173,328,990 | 173,417,537 | 88,548 |
ENST00000417539.1 | hg19 | chr2 | 173,329,875 | 173,330,740 | 866 |
ENST00000442417.5 | hg19 | chr2 | 173,345,568 | 173,421,257 | 75,690 |
ENST00000450443.1 | hg19 | chr2 | 173,368,167 | 173,421,324 | 53,158 |
ENST00000416080.1 | hg19 | chr2 | 173,373,757 | 173,377,238 | 3,482 |
Genome browser