UXT ubiquitously expressed prefoldin like chaperone
Information
- Symbol
- UXT
- Type
- protein-coding
- Description
- ubiquitously expressed prefoldin like chaperone
- Entrez Gene ID
- 8409
- Genome
- hg19
- Position
- chrX:47,511,195-47,518,579
- Genome
- hg38
- Position
- chrX:47,651,796-47,659,180
- MIM
- 300234 OMIM
- HGNC
- HGNC:12641 HGNC
- Ensembl
- ENSG00000126756 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
10 |
![]() |
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 | ART-27 |
SYNONYM | SKP2 |
SYNONYM | STAP1 |
MIM | 300234 OMIM |
HGNC | HGNC:12641 HGNC |
Ensembl | ENSG00000126756 Ensembl |
AllianceGenome | HGNC:12641 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000333119.8 | hg38 | chrX | 47,651,796 | 47,659,180 | 7,385 |
ENST00000335890.3 | hg38 | chrX | 47,651,796 | 47,659,180 | 7,385 |
ENST00000333119.8 | hg19 | chrX | 47,511,195 | 47,518,579 | 7,385 |
ENST00000335890.3 | hg19 | chrX | 47,511,195 | 47,518,579 | 7,385 |
Genome browser