SNHG1 small nucleolar RNA host gene 1
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 | LINC00057 |
SYNONYM | NCRNA00057 |
SYNONYM | U22HG |
SYNONYM | UHG |
SYNONYM | lncRNA16 |
MIM | 603222 OMIM |
HGNC | HGNC:32688 HGNC |
Ensembl | ENSG00000255717 Ensembl |
AllianceGenome | HGNC:32688 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000660730.1 | hg38 | chr11 | 62,851,999 | 62,855,837 | 3,839 |
ENST00000668309.1 | hg38 | chr11 | 62,852,138 | 62,855,856 | 3,719 |
ENST00000670502.1 | hg38 | chr11 | 62,852,036 | 62,855,906 | 3,871 |
ENST00000692454.1 | hg38 | chr11 | 62,851,988 | 62,855,885 | 3,898 |
ENST00000660730.1 | hg19 | chr11 | 62,619,471 | 62,623,309 | 3,839 |
ENST00000668309.1 | hg19 | chr11 | 62,619,610 | 62,623,328 | 3,719 |
ENST00000670502.1 | hg19 | chr11 | 62,619,508 | 62,623,378 | 3,871 |
ENST00000692454.1 | hg19 | chr11 | 62,619,460 | 62,623,357 | 3,898 |
Genome browser