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 | |
|---|---|
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0 |
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0 |
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0 |
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10 |
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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
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| 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
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| 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
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| Category | : |
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| 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 |
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