LINC02763 long intergenic non-protein coding RNA 2763
Information
- Symbol
- LINC02763
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 2763
- Entrez Gene ID
- 101928823
- Genome
- hg19
- Position
- chr11:112,263,897-112,495,290
- Genome
- hg38
- Position
- chr11:112,393,174-112,624,567
- HGNC
- HGNC:54282 HGNC
- Ensembl
- ENSG00000254968 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 |
---|---|---|---|---|---|
ENST00000671165.1 | hg38 | chr11 | 112,482,142 | 112,488,377 | 6,236 |
ENST00000665326.1 | hg38 | chr11 | 112,393,174 | 112,624,567 | 231,394 |
ENST00000528496.1 | hg38 | chr11 | 112,393,118 | 112,541,916 | 148,799 |
ENST00000529238.5 | hg38 | chr11 | 112,482,232 | 112,621,729 | 139,498 |
ENST00000528496.1 | hg19 | chr11 | 112,263,841 | 112,412,639 | 148,799 |
ENST00000665326.1 | hg19 | chr11 | 112,263,897 | 112,495,290 | 231,394 |
ENST00000671165.1 | hg19 | chr11 | 112,352,865 | 112,359,100 | 6,236 |
ENST00000529238.5 | hg19 | chr11 | 112,352,955 | 112,492,452 | 139,498 |
Genome browser