MYL12A myosin light chain 12A
Information
- Symbol
- MYL12A
- Type
- protein-coding
- Description
- myosin light chain 12A
- Entrez Gene ID
- 10627
- Genome
- hg19
- Position
- chr18:3,252,273-3,256,233
- Genome
- hg38
- Position
- chr18:3,252,275-3,256,235
- HGNC
- HGNC:16701 HGNC
- Ensembl
- ENSG00000101608 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Uncertain significance | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
10 |
 |
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
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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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| 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 | HEL-S-24 |
| SYNONYM | MLC-2B |
| SYNONYM | MLCB |
| SYNONYM | MRCL3 |
| SYNONYM | MRLC3 |
| SYNONYM | MYL2B |
| HGNC | HGNC:16701 HGNC |
| Ensembl | ENSG00000101608 Ensembl |
| AllianceGenome | HGNC:16701 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000580887.5 | hg38 | chr18 | 3,252,275 | 3,256,235 | 3,961 |
| ENST00000217652.8 | hg38 | chr18 | 3,247,801 | 3,256,236 | 8,436 |
| ENST00000578611.5 | hg38 | chr18 | 3,247,813 | 3,256,211 | 8,399 |
| ENST00000536605.1 | hg38 | chr18 | 3,252,275 | 3,256,235 | 3,961 |
| ENST00000579226.5 | hg38 | chr18 | 3,247,481 | 3,256,227 | 8,747 |
| ENST00000579226.5 | hg19 | chr18 | 3,247,479 | 3,256,225 | 8,747 |
| ENST00000217652.8 | hg19 | chr18 | 3,247,799 | 3,256,234 | 8,436 |
| ENST00000578611.5 | hg19 | chr18 | 3,247,811 | 3,256,209 | 8,399 |
| ENST00000536605.1 | hg19 | chr18 | 3,252,273 | 3,256,233 | 3,961 |
| ENST00000580887.5 | hg19 | chr18 | 3,252,273 | 3,256,233 | 3,961 |
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