CDC37 cell division cycle 37, HSP90 cochaperone
Information
- Symbol
- CDC37
- Type
- protein-coding
- Description
- cell division cycle 37, HSP90 cochaperone
- Entrez Gene ID
- 11140
- Genome
- hg19
- Position
- chr19:10,501,809-10,514,218
- Genome
- hg38
- Position
- chr19:10,391,133-10,403,542
- MIM
- 605065 OMIM
- HGNC
- HGNC:1735 HGNC
- Ensembl
- ENSG00000105401 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
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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32 |
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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 |
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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 | P50CDC37 |
MIM | 605065 OMIM |
HGNC | HGNC:1735 HGNC |
Ensembl | ENSG00000105401 Ensembl |
AllianceGenome | HGNC:1735 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000222005.7 | hg38 | chr19 | 10,391,133 | 10,403,542 | 12,410 |
ENST00000222005.7 | hg19 | chr19 | 10,501,809 | 10,514,218 | 12,410 |
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