ST14 ST14 transmembrane serine protease matriptase
Information
- Symbol
- ST14
- Type
- protein-coding
- Description
- ST14 transmembrane serine protease matriptase
- Entrez Gene ID
- 6768
- Genome
- hg19
- Position
- chr11:130,029,677-130,080,257
- Genome
- hg38
- Position
- chr11:130,159,782-130,210,362
- MIM
- 606797 OMIM
- HGNC
- HGNC:11344 HGNC
- Ensembl
- ENSG00000149418 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 2 | 14 |
Likely pathogenic | 0 | 8 |
Benign | 0 | 128 |
Likely benign | 0 | 88 |
Conflicting classifications of pathogenicity | 0 | 4 |
Uncertain significance | 0 | 104 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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48 |
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272 |
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12 |
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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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
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Category | : |
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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 | ARCI11 |
SYNONYM | CAP3 |
SYNONYM | HAI |
SYNONYM | MT-SP1 |
SYNONYM | MTSP1 |
SYNONYM | PRSS14 |
SYNONYM | SNC19 |
SYNONYM | TADG15 |
SYNONYM | TMPRSS14 |
MIM | 606797 OMIM |
HGNC | HGNC:11344 HGNC |
Ensembl | ENSG00000149418 Ensembl |
AllianceGenome | HGNC:11344 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000278742.6 | hg38 | chr11 | 130,159,782 | 130,210,362 | 50,581 |
ENST00000278742.6 | hg19 | chr11 | 130,029,677 | 130,080,257 | 50,581 |
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