LINC01241 long intergenic non-protein coding RNA 1241
Information
- Symbol
- LINC01241
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1241
- Entrez Gene ID
- 101929582
- Genome
- hg19
- Position
- chr9:25,780,075-25,812,962
- Genome
- hg38
- Position
- chr9:25,780,077-25,812,964
- HGNC
- HGNC:49804 HGNC
- Ensembl
- ENSG00000236306 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 |
---|---|---|---|---|---|
ENST00000654259.1 | hg38 | chr9 | 25,780,077 | 25,812,964 | 32,888 |
ENST00000668254.1 | hg38 | chr9 | 25,780,032 | 25,785,312 | 5,281 |
ENST00000663468.1 | hg38 | chr9 | 25,780,043 | 25,816,502 | 36,460 |
ENST00000627303.1 | hg38 | chr9 | 25,804,187 | 25,812,967 | 8,781 |
ENST00000423326.2 | hg38 | chr9 | 25,780,056 | 25,812,968 | 32,913 |
ENST00000668254.1 | hg19 | chr9 | 25,780,030 | 25,785,310 | 5,281 |
ENST00000663468.1 | hg19 | chr9 | 25,780,041 | 25,816,500 | 36,460 |
ENST00000423326.2 | hg19 | chr9 | 25,780,054 | 25,812,966 | 32,913 |
ENST00000654259.1 | hg19 | chr9 | 25,780,075 | 25,812,962 | 32,888 |
ENST00000627303.1 | hg19 | chr9 | 25,804,185 | 25,812,965 | 8,781 |
Genome browser