MCRIP2 MAPK regulated corepressor interacting protein 2
Information
- Symbol
- MCRIP2
- Type
- protein-coding
- Description
- MAPK regulated corepressor interacting protein 2
- Entrez Gene ID
- 84331
- Genome
- hg19
- Position
- chr16:691,828-698,474
- Genome
- hg38
- Position
- chr16:641,828-648,474
- HGNC
- HGNC:14142 HGNC
- Ensembl
- ENSG00000172366 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 2 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
2 |
 |
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
[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 | C16orf14 |
| SYNONYM | FAM195A |
| SYNONYM | c349E10.1 |
| HGNC | HGNC:14142 HGNC |
| Ensembl | ENSG00000172366 Ensembl |
| AllianceGenome | HGNC:14142 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000307650.9 | hg38 | chr16 | 641,828 | 648,474 | 6,647 |
| ENST00000629534.2 | hg38 | chr16 | 641,849 | 646,487 | 4,639 |
| ENST00000307650.9 | hg19 | chr16 | 691,828 | 698,474 | 6,647 |
| ENST00000629534.2 | hg19 | chr16 | 691,849 | 696,487 | 4,639 |
Genome browser