TMPRSS13 transmembrane serine protease 13
Information
- Symbol
- TMPRSS13
- Type
- protein-coding
- Description
- transmembrane serine protease 13
- Entrez Gene ID
- 84000
- Genome
- hg19
- Position
- chr11:117,771,356-117,800,117
- Genome
- hg38
- Position
- chr11:117,900,641-117,929,402
- MIM
- 610050 OMIM
- HGNC
- HGNC:29808 HGNC
- Ensembl
- ENSG00000137747 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 72 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
74 |
 |
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 |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| 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 | MSP |
| SYNONYM | MSPL |
| SYNONYM | MSPS |
| SYNONYM | TMPRSS11 |
| MIM | 610050 OMIM |
| HGNC | HGNC:29808 HGNC |
| Ensembl | ENSG00000137747 Ensembl |
| AllianceGenome | HGNC:29808 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000524993.6 | hg38 | chr11 | 117,900,641 | 117,929,402 | 28,762 |
| ENST00000430170.6 | hg38 | chr11 | 117,903,042 | 117,929,395 | 26,354 |
| ENST00000445164.6 | hg38 | chr11 | 117,903,045 | 117,929,381 | 26,337 |
| ENST00000528626.5 | hg38 | chr11 | 117,900,643 | 117,929,381 | 28,739 |
| ENST00000526090.1 | hg38 | chr11 | 117,907,454 | 117,929,459 | 22,006 |
| ENST00000524993.6 | hg19 | chr11 | 117,771,356 | 117,800,117 | 28,762 |
| ENST00000528626.5 | hg19 | chr11 | 117,771,358 | 117,800,096 | 28,739 |
| ENST00000430170.6 | hg19 | chr11 | 117,773,757 | 117,800,110 | 26,354 |
| ENST00000445164.6 | hg19 | chr11 | 117,773,760 | 117,800,096 | 26,337 |
| ENST00000526090.1 | hg19 | chr11 | 117,778,169 | 117,800,174 | 22,006 |
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