LYL1 LYL1 basic helix-loop-helix family member
Information
- Symbol
- LYL1
- Type
- protein-coding
- Description
- LYL1 basic helix-loop-helix family member
- Entrez Gene ID
- 4066
- Genome
- hg19
- Position
- chr19:13,209,847-13,213,672
- Genome
- hg38
- Position
- chr19:13,099,033-13,102,858
- MIM
- 151440 OMIM
- HGNC
- HGNC:6734 HGNC
- Ensembl
- ENSG00000104903 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 | bHLHa18 |
MIM | 151440 OMIM |
HGNC | HGNC:6734 HGNC |
Ensembl | ENSG00000104903 Ensembl |
AllianceGenome | HGNC:6734 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000264824.5 | hg38 | chr19 | 13,099,033 | 13,102,858 | 3,826 |
ENST00000264824.5 | hg19 | chr19 | 13,209,847 | 13,213,672 | 3,826 |
Key | Value |
---|---|
strand | - |
UniProt | OG |
start | 13,209,841 |
Gene Symbol | LYL1 |
Entrez GeneId | 4,066 |
Chr Band | 19p13.2-p13.1 |
end | 13,213,973 |
chr | chr19 |
Name | lymphoblastic leukemia derived sequence 1 |
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