EMSY EMSY transcriptional repressor, BRCA2 interacting
Information
- Symbol
- EMSY
- Type
- protein-coding
- Description
- EMSY transcriptional repressor, BRCA2 interacting
- Entrez Gene ID
- 56946
- Genome
- hg19
- Position
- chr11:76,156,062-76,264,075
- Genome
- hg38
- Position
- chr11:76,445,018-76,553,031
- MIM
- 608574 OMIM
- HGNC
- HGNC:18071 HGNC
- Ensembl
- ENSG00000158636 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 16 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 18 |
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
[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 | C11orf30 |
SYNONYM | GL002 |
MIM | 608574 OMIM |
HGNC | HGNC:18071 HGNC |
Ensembl | ENSG00000158636 Ensembl |
AllianceGenome | HGNC:18071 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000525038.5 | hg38 | chr11 | 76,446,900 | 76,550,511 | 103,612 |
ENST00000695367.1 | hg38 | chr11 | 76,445,018 | 76,553,031 | 108,014 |
ENST00000334736.7 | hg38 | chr11 | 76,445,025 | 76,551,542 | 106,518 |
ENST00000533988.5 | hg38 | chr11 | 76,445,022 | 76,453,931 | 8,910 |
ENST00000533248.5 | hg38 | chr11 | 76,446,900 | 76,550,209 | 103,310 |
ENST00000524490.5 | hg38 | chr11 | 76,445,025 | 76,550,343 | 105,319 |
ENST00000525919.5 | hg38 | chr11 | 76,446,900 | 76,550,209 | 103,310 |
ENST00000524767.5 | hg38 | chr11 | 76,446,900 | 76,550,209 | 103,310 |
ENST00000529032.5 | hg38 | chr11 | 76,446,939 | 76,553,025 | 106,087 |
ENST00000524490.5 | hg19 | chr11 | 76,156,069 | 76,261,387 | 105,319 |
ENST00000334736.7 | hg19 | chr11 | 76,156,069 | 76,262,586 | 106,518 |
ENST00000524767.5 | hg19 | chr11 | 76,157,944 | 76,261,253 | 103,310 |
ENST00000525919.5 | hg19 | chr11 | 76,157,944 | 76,261,253 | 103,310 |
ENST00000525038.5 | hg19 | chr11 | 76,157,944 | 76,261,555 | 103,612 |
ENST00000529032.5 | hg19 | chr11 | 76,157,983 | 76,264,069 | 106,087 |
ENST00000533248.5 | hg19 | chr11 | 76,157,944 | 76,261,253 | 103,310 |
ENST00000533988.5 | hg19 | chr11 | 76,156,066 | 76,164,975 | 8,910 |
ENST00000695367.1 | hg19 | chr11 | 76,156,062 | 76,264,075 | 108,014 |
Genome browser