RUSF1 RUS family member 1
Information
- Symbol
- RUSF1
- Type
- protein-coding
- Description
- RUS family member 1
- Entrez Gene ID
- 64755
- Genome
- hg19
- Position
- chr16:31,500,796-31,519,712
- Genome
- hg38
- Position
- chr16:31,489,475-31,508,391
- HGNC
- HGNC:25848 HGNC
- Ensembl
- ENSG00000140688 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 10 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
8 |
![]() |
64 |
![]() |
2 |
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 | C16orf58 |
SYNONYM | RUS |
HGNC | HGNC:25848 HGNC |
Ensembl | ENSG00000140688 Ensembl |
AllianceGenome | HGNC:25848 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000567994.5 | hg38 | chr16 | 31,490,273 | 31,508,384 | 18,112 |
ENST00000570164.5 | hg38 | chr16 | 31,489,471 | 31,508,391 | 18,921 |
ENST00000327237.7 | hg38 | chr16 | 31,489,475 | 31,508,391 | 18,917 |
ENST00000570164.5 | hg19 | chr16 | 31,500,792 | 31,519,712 | 18,921 |
ENST00000327237.7 | hg19 | chr16 | 31,500,796 | 31,519,712 | 18,917 |
ENST00000567994.5 | hg19 | chr16 | 31,501,594 | 31,519,705 | 18,112 |
Genome browser