BLACE B cell acute lymphoblastic leukemia expressed
Information
- Symbol
- BLACE
- Type
- ncRNA
- Description
- B cell acute lymphoblastic leukemia expressed
- Entrez Gene ID
- 338436
- Genome
- hg19
- Position
- chr7:155,149,680-155,160,629
- Genome
- hg38
- Position
- chr7:155,356,985-155,367,934
- MIM
- 608450 OMIM
- HGNC
- HGNC:20484 HGNC
- Ensembl
- ENSG00000204960 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Ranking
ClinVar | |
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0 |
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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
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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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 |
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MIM | 608450 OMIM |
HGNC | HGNC:20484 HGNC |
Ensembl | ENSG00000204960 Ensembl |
AllianceGenome | HGNC:20484 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000378120.5 | hg38 | chr7 | 155,356,985 | 155,367,934 | 10,950 |
ENST00000378120.5 | hg19 | chr7 | 155,149,680 | 155,160,629 | 10,950 |
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