IMP3 IMP U3 small nucleolar ribonucleoprotein 3
Information
- Symbol
- IMP3
- Type
- protein-coding
- Description
- IMP U3 small nucleolar ribonucleoprotein 3
- Entrez Gene ID
- 55272
- Genome
- hg19
- Position
- chr15:75,931,426-75,941,047
- Genome
- hg38
- Position
- chr15:75,639,085-75,648,706
- MIM
- 612980 OMIM
- HGNC
- HGNC:14497 HGNC
- Ensembl
- ENSG00000177971 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 1 | 0 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
36 |
 |
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 | BRMS2 |
| SYNONYM | C15orf12 |
| SYNONYM | MRPS4 |
| MIM | 612980 OMIM |
| HGNC | HGNC:14497 HGNC |
| Ensembl | ENSG00000177971 Ensembl |
| AllianceGenome | HGNC:14497 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000314852.2 | hg38 | chr15 | 75,639,085 | 75,648,706 | 9,622 |
| ENST00000403490.3 | hg38 | chr15 | 75,639,093 | 75,640,224 | 1,132 |
| ENST00000314852.2 | hg19 | chr15 | 75,931,426 | 75,941,047 | 9,622 |
| ENST00000403490.3 | hg19 | chr15 | 75,931,434 | 75,932,565 | 1,132 |
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