LINC01446 long intergenic non-protein coding RNA 1446
Information
- Symbol
- LINC01446
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 1446
- Entrez Gene ID
- 401337
- Genome
- hg19
- Position
- chr7:53,723,202-53,879,624
- Genome
- hg38
- Position
- chr7:53,655,509-53,811,931
- HGNC
- HGNC:50773 HGNC
- Ensembl
- ENSG00000205628 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
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
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 | GS1-179L18.1 |
HGNC | HGNC:50773 HGNC |
Ensembl | ENSG00000205628 Ensembl |
AllianceGenome | HGNC:50773 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000670902.1 | hg38 | chr7 | 53,655,508 | 53,780,235 | 124,728 |
ENST00000652440.1 | hg38 | chr7 | 53,691,177 | 53,811,942 | 120,766 |
ENST00000652104.1 | hg38 | chr7 | 53,765,495 | 53,811,942 | 46,448 |
ENST00000669638.1 | hg38 | chr7 | 53,691,186 | 53,811,931 | 120,746 |
ENST00000668489.1 | hg38 | chr7 | 53,764,481 | 53,811,928 | 47,448 |
ENST00000380970.2 | hg38 | chr7 | 53,655,509 | 53,811,931 | 156,423 |
ENST00000656885.1 | hg38 | chr7 | 53,770,080 | 53,811,942 | 41,863 |
ENST00000380970.2 | hg19 | chr7 | 53,723,202 | 53,879,624 | 156,423 |
ENST00000669638.1 | hg19 | chr7 | 53,758,879 | 53,879,624 | 120,746 |
ENST00000668489.1 | hg19 | chr7 | 53,832,174 | 53,879,621 | 47,448 |
ENST00000652104.1 | hg19 | chr7 | 53,833,188 | 53,879,635 | 46,448 |
ENST00000656885.1 | hg19 | chr7 | 53,837,773 | 53,879,635 | 41,863 |
ENST00000670902.1 | hg19 | chr7 | 53,723,201 | 53,847,928 | 124,728 |
ENST00000652440.1 | hg19 | chr7 | 53,758,870 | 53,879,635 | 120,766 |
Genome browser