LSM5 LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated
Information
- Symbol
- LSM5
- Type
- protein-coding
- Description
- LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated
- Entrez Gene ID
- 23658
- Genome
- hg19
- Position
- chr7:32,524,950-32,529,992
- Genome
- hg38
- Position
- chr7:32,485,338-32,490,380
- MIM
- 607285 OMIM
- HGNC
- HGNC:17162 HGNC
- Ensembl
- ENSG00000106355 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
4 |
![]() |
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 | YER146W |
MIM | 607285 OMIM |
HGNC | HGNC:17162 HGNC |
Ensembl | ENSG00000106355 Ensembl |
AllianceGenome | HGNC:17162 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409292.5 | hg38 | chr7 | 32,487,029 | 32,490,100 | 3,072 |
ENST00000409952.3 | hg38 | chr7 | 32,487,063 | 32,495,249 | 8,187 |
ENST00000450169.7 | hg38 | chr7 | 32,485,338 | 32,490,380 | 5,043 |
ENST00000410044.5 | hg38 | chr7 | 32,487,035 | 32,490,361 | 3,327 |
ENST00000409782.5 | hg38 | chr7 | 32,487,040 | 32,490,380 | 3,341 |
ENST00000409909.7 | hg38 | chr7 | 32,486,805 | 32,495,283 | 8,479 |
ENST00000409987.5 | hg38 | chr7 | 32,487,035 | 32,490,380 | 3,346 |
ENST00000450169.7 | hg19 | chr7 | 32,524,950 | 32,529,992 | 5,043 |
ENST00000409909.7 | hg19 | chr7 | 32,526,417 | 32,534,895 | 8,479 |
ENST00000409292.5 | hg19 | chr7 | 32,526,641 | 32,529,712 | 3,072 |
ENST00000410044.5 | hg19 | chr7 | 32,526,647 | 32,529,973 | 3,327 |
ENST00000409987.5 | hg19 | chr7 | 32,526,647 | 32,529,992 | 3,346 |
ENST00000409782.5 | hg19 | chr7 | 32,526,652 | 32,529,992 | 3,341 |
ENST00000409952.3 | hg19 | chr7 | 32,526,675 | 32,534,861 | 8,187 |
Genome browser