TM4SF20 transmembrane 4 L six family member 20
Information
- Symbol
- TM4SF20
- Type
- protein-coding
- Description
- transmembrane 4 L six family member 20
- Entrez Gene ID
- 79853
- Genome
- hg19
- Position
- chr2:228,226,754-228,244,022
- Genome
- hg38
- Position
- chr2:227,362,038-227,379,306
- MIM
- 615404 OMIM
- HGNC
- HGNC:26230 HGNC
- Ensembl
- ENSG00000168955 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 18 |
Likely benign | 0 | 30 |
Uncertain significance | 0 | 60 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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22 |
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86 |
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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 |
Prediction | |||||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | PRO994 |
SYNONYM | SLI5 |
SYNONYM | TCCE518 |
MIM | 615404 OMIM |
HGNC | HGNC:26230 HGNC |
Ensembl | ENSG00000168955 Ensembl |
AllianceGenome | HGNC:26230 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000304568.4 | hg38 | chr2 | 227,362,038 | 227,379,306 | 17,269 |
ENST00000304568.4 | hg19 | chr2 | 228,226,754 | 228,244,022 | 17,269 |
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