ASCL1 achaete-scute family bHLH transcription factor 1
Information
- Symbol
- ASCL1
- Type
- protein-coding
- Description
- achaete-scute family bHLH transcription factor 1
- Entrez Gene ID
- 429
- Genome
- hg19
- Position
- chr12:103,351,452-103,354,291
- Genome
- hg38
- Position
- chr12:102,957,674-102,960,513
- MIM
- 100790 OMIM
- HGNC
- HGNC:738 HGNC
- Ensembl
- ENSG00000139352 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 32 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
8 |
 |
28 |
 |
6 |
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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| 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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| 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 | ASH1 |
| SYNONYM | HASH1 |
| SYNONYM | MASH1 |
| SYNONYM | bHLHa46 |
| MIM | 100790 OMIM |
| HGNC | HGNC:738 HGNC |
| Ensembl | ENSG00000139352 Ensembl |
| AllianceGenome | HGNC:738 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000266744.4 | hg38 | chr12 | 102,957,674 | 102,960,513 | 2,840 |
| ENST00000266744.4 | hg19 | chr12 | 103,351,452 | 103,354,291 | 2,840 |
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