SCUBE3 signal peptide, CUB domain and EGF like domain containing 3
Information
- Symbol
- SCUBE3
- Type
- protein-coding
- Description
- signal peptide, CUB domain and EGF like domain containing 3
- Entrez Gene ID
- 222663
- Genome
- hg19
- Position
- chr6:35,181,733-35,220,856
- Genome
- hg38
- Position
- chr6:35,213,956-35,253,079
- MIM
- 614708 OMIM
- HGNC
- HGNC:13655 HGNC
- Ensembl
- ENSG00000146197 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 16 |
Likely pathogenic | 0 | 2 |
Benign | 0 | 8 |
Likely benign | 0 | 2 |
not provided | 1 | 0 |
Uncertain significance | 0 | 120 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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142 |
![]() |
2 |
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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Category | : |
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Search word | : | |
Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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 | CEGF3 |
SYNONYM | SSFSC2 |
MIM | 614708 OMIM |
HGNC | HGNC:13655 HGNC |
Ensembl | ENSG00000146197 Ensembl |
AllianceGenome | HGNC:13655 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000274938.8 | hg38 | chr6 | 35,213,956 | 35,253,079 | 39,124 |
ENST00000274938.8 | hg19 | chr6 | 35,181,733 | 35,220,856 | 39,124 |
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