UTP14A UTP14A small subunit processome component
Information
- Symbol
- UTP14A
- Type
- protein-coding
- Description
- UTP14A small subunit processome component
- Entrez Gene ID
- 10813
- Genome
- hg19
- Position
- chrX:129,040,140-129,063,728
- Genome
- hg38
- Position
- chrX:129,906,164-129,929,752
- MIM
- 300508 OMIM
- HGNC
- HGNC:10665 HGNC
- Ensembl
- ENSG00000156697 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 12 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 68 |
Ranking
| ClinVar | |
|---|---|
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0 |
![]() |
0 |
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2 |
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80 |
![]() |
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 | NYCO16 |
| SYNONYM | SDCCAG16 |
| SYNONYM | Utp14 |
| SYNONYM | dJ537K23.3 |
| MIM | 300508 OMIM |
| HGNC | HGNC:10665 HGNC |
| Ensembl | ENSG00000156697 Ensembl |
| AllianceGenome | HGNC:10665 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000394422.8 | hg38 | chrX | 129,906,164 | 129,929,752 | 23,589 |
| ENST00000425117.6 | hg38 | chrX | 129,906,121 | 129,929,761 | 23,641 |
| ENST00000425117.6 | hg19 | chrX | 129,040,097 | 129,063,737 | 23,641 |
| ENST00000394422.8 | hg19 | chrX | 129,040,140 | 129,063,728 | 23,589 |
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