ASCL2 achaete-scute family bHLH transcription factor 2
Information
- Symbol
- ASCL2
- Type
- protein-coding
- Description
- achaete-scute family bHLH transcription factor 2
- Entrez Gene ID
- 430
- Genome
- hg19
- Position
- chr11:2,289,728-2,291,818
- Genome
- hg38
- Position
- chr11:2,268,498-2,270,588
- MIM
- 601886 OMIM
- HGNC
- HGNC:739 HGNC
- Ensembl
- ENSG00000183734 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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26 |
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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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | ASH2 |
SYNONYM | HASH2 |
SYNONYM | MASH2 |
SYNONYM | bHLHa45 |
MIM | 601886 OMIM |
HGNC | HGNC:739 HGNC |
Ensembl | ENSG00000183734 Ensembl |
AllianceGenome | HGNC:739 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000331289.5 | hg38 | chr11 | 2,268,498 | 2,270,588 | 2,091 |
ENST00000331289.5 | hg19 | chr11 | 2,289,728 | 2,291,818 | 2,091 |
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