SUV39H1 SUV39H1 histone lysine methyltransferase
Information
- Symbol
- SUV39H1
- Type
- protein-coding
- Description
- SUV39H1 histone lysine methyltransferase
- Entrez Gene ID
- 6839
- Genome
- hg19
- Position
- chrX:48,553,945-48,567,401
- Genome
- hg38
- Position
- chrX:48,695,554-48,709,010
- MIM
- 300254 OMIM
- HGNC
- HGNC:11479 HGNC
- Ensembl
- ENSG00000101945 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 4 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
12 |
 |
2 |
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 | H3-K9-HMTase 1 |
| SYNONYM | KMT1A |
| SYNONYM | MG44 |
| SYNONYM | SUV39H |
| MIM | 300254 OMIM |
| HGNC | HGNC:11479 HGNC |
| Ensembl | ENSG00000101945 Ensembl |
| AllianceGenome | HGNC:11479 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000376687.4 | hg38 | chrX | 48,696,734 | 48,709,016 | 12,283 |
| ENST00000337852.10 | hg38 | chrX | 48,695,554 | 48,709,010 | 13,457 |
| ENST00000337852.10 | hg19 | chrX | 48,553,945 | 48,567,401 | 13,457 |
| ENST00000376687.4 | hg19 | chrX | 48,555,125 | 48,567,407 | 12,283 |
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