LIN37 lin-37 DREAM MuvB core complex component
Information
- Symbol
- LIN37
- Type
- protein-coding
- Description
- lin-37 DREAM MuvB core complex component
- Entrez Gene ID
- 55957
- Genome
- hg19
- Position
- chr19:36,239,477-36,245,420
- Genome
- hg38
- Position
- chr19:35,748,576-35,754,519
- HGNC
- HGNC:33234 HGNC
- Ensembl
- ENSG00000267796 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
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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 |
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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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | F25965 |
SYNONYM | ZK418.4 |
SYNONYM | lin-37 |
HGNC | HGNC:33234 HGNC |
Ensembl | ENSG00000267796 Ensembl |
AllianceGenome | HGNC:33234 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000301159.14 | hg38 | chr19 | 35,748,576 | 35,754,519 | 5,944 |
ENST00000301159.14 | hg19 | chr19 | 36,239,477 | 36,245,420 | 5,944 |
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