TSPAN4 tetraspanin 4
Clinical Significance
MGeND | ClinVar | |
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Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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
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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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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 |
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SYNONYM | NAG-2 |
SYNONYM | NAG2 |
SYNONYM | TETRASPAN |
SYNONYM | TM4SF7 |
SYNONYM | TSPAN-4 |
MIM | 602644 OMIM |
HGNC | HGNC:11859 HGNC |
Ensembl | ENSG00000214063 Ensembl |
AllianceGenome | HGNC:11859 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000409543.6 | hg38 | chr11 | 844,117 | 866,857 | 22,741 |
ENST00000397397.7 | hg38 | chr11 | 842,852 | 867,111 | 24,260 |
ENST00000397396.5 | hg38 | chr11 | 842,824 | 867,116 | 24,293 |
ENST00000346501.8 | hg38 | chr11 | 847,197 | 866,776 | 19,580 |
ENST00000409531.5 | hg38 | chr11 | 848,810 | 867,111 | 18,302 |
ENST00000397411.6 | hg38 | chr11 | 842,812 | 866,817 | 24,006 |
ENST00000397408.5 | hg38 | chr11 | 842,941 | 867,116 | 24,176 |
ENST00000527644.2 | hg38 | chr11 | 849,816 | 867,111 | 17,296 |
ENST00000397404.5 | hg38 | chr11 | 844,446 | 867,116 | 22,671 |
ENST00000397406.5 | hg38 | chr11 | 844,081 | 867,116 | 23,036 |
ENST00000525201.5 | hg38 | chr11 | 844,153 | 866,676 | 22,524 |
ENST00000397396.5 | hg19 | chr11 | 842,824 | 867,116 | 24,293 |
ENST00000397397.7 | hg19 | chr11 | 842,852 | 867,111 | 24,260 |
ENST00000397408.5 | hg19 | chr11 | 842,941 | 867,116 | 24,176 |
ENST00000397411.6 | hg19 | chr11 | 842,812 | 866,817 | 24,006 |
ENST00000397406.5 | hg19 | chr11 | 844,081 | 867,116 | 23,036 |
ENST00000409543.6 | hg19 | chr11 | 844,117 | 866,857 | 22,741 |
ENST00000397404.5 | hg19 | chr11 | 844,446 | 867,116 | 22,671 |
ENST00000346501.8 | hg19 | chr11 | 847,197 | 866,776 | 19,580 |
ENST00000409531.5 | hg19 | chr11 | 848,810 | 867,111 | 18,302 |
ENST00000525201.5 | hg19 | chr11 | 844,153 | 866,676 | 22,524 |
ENST00000527644.2 | hg19 | chr11 | 849,816 | 867,111 | 17,296 |
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