ASMTL acetylserotonin O-methyltransferase like
Information
- Symbol
- ASMTL
- Type
- protein-coding
- Description
- acetylserotonin O-methyltransferase like
- Entrez Gene ID
- 8623
- Genome
- hg19
- Position
- chrX:1,522,032-1,571,802
- Genome
- hg19
- Position
- chrY:1,472,032-1,521,802
- Genome
- hg38
- Position
- chrY:1,403,139-1,452,909
- Genome
- hg38
- Position
- chrX:1,403,139-1,452,909
- MIM
- 300162 OMIM
- HGNC
- HGNC:751 HGNC
- Ensembl
- ENSG00000169093 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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0 |
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4 |
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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Category | : |
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Search word | : | |
Filtering | : |
Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | ASMTLX |
SYNONYM | ASMTLY |
SYNONYM | ASTML |
MIM | 300162 OMIM |
MIM | 400011 OMIM |
HGNC | HGNC:751 HGNC |
Ensembl | ENSG00000169093 Ensembl |
Ensembl | ENSG00000292339 Ensembl |
AllianceGenome | HGNC:751 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000534940.6 | hg38 | chrX | 1,403,139 | 1,453,762 | 50,624 |
ENST00000711192.1 | hg38 | chrY | 1,403,139 | 1,453,762 | 50,624 |
ENST00000711197.1 | hg38 | chrY | 1,403,139 | 1,452,909 | 49,771 |
ENST00000711196.1 | hg38 | chrY | 1,403,141 | 1,452,929 | 49,789 |
ENST00000381317.9 | hg38 | chrX | 1,403,139 | 1,452,909 | 49,771 |
ENST00000381333.9 | hg38 | chrX | 1,403,141 | 1,452,929 | 49,789 |
ENST00000381317.9 | hg19 | chrX | 1,522,032 | 1,571,802 | 49,771 |
ENST00000534940.6 | hg19 | chrX | 1,522,032 | 1,572,655 | 50,624 |
ENST00000381333.9 | hg19 | chrX | 1,522,034 | 1,571,822 | 49,789 |
ENST00000711197.1 | hg19 | chrY | 1,472,032 | 1,521,802 | 49,771 |
ENST00000711192.1 | hg19 | chrY | 1,472,032 | 1,522,655 | 50,624 |
ENST00000711196.1 | hg19 | chrY | 1,472,034 | 1,521,822 | 49,789 |
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