MPP2 MAGUK p55 scaffold protein 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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44 |
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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 |
Search Word
Target data | : |
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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | DLG2 |
MIM | 600723 OMIM |
HGNC | HGNC:7220 HGNC |
Ensembl | ENSG00000108852 Ensembl |
AllianceGenome | HGNC:7220 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000520305.5 | hg38 | chr17 | 43,877,332 | 43,907,536 | 30,205 |
ENST00000518766.5 | hg38 | chr17 | 43,877,762 | 43,909,700 | 31,939 |
ENST00000622681.4 | hg38 | chr17 | 43,875,363 | 43,909,711 | 34,349 |
ENST00000461854.5 | hg38 | chr17 | 43,876,162 | 43,907,526 | 31,365 |
ENST00000612133.4 | hg38 | chr17 | 43,875,363 | 43,907,942 | 32,580 |
ENST00000269095.9 | hg38 | chr17 | 43,875,360 | 43,907,536 | 32,177 |
ENST00000536246.5 | hg38 | chr17 | 43,875,363 | 43,901,562 | 26,200 |
ENST00000377184.7 | hg38 | chr17 | 43,875,357 | 43,900,598 | 25,242 |
ENST00000523501.5 | hg38 | chr17 | 43,877,377 | 43,907,536 | 30,160 |
ENST00000269095.9 | hg19 | chr17 | 41,952,728 | 41,984,904 | 32,177 |
ENST00000377184.7 | hg19 | chr17 | 41,952,725 | 41,977,966 | 25,242 |
ENST00000461854.5 | hg19 | chr17 | 41,953,530 | 41,984,894 | 31,365 |
ENST00000518766.5 | hg19 | chr17 | 41,955,130 | 41,987,068 | 31,939 |
ENST00000520305.5 | hg19 | chr17 | 41,954,700 | 41,984,904 | 30,205 |
ENST00000523501.5 | hg19 | chr17 | 41,954,745 | 41,984,904 | 30,160 |
ENST00000536246.5 | hg19 | chr17 | 41,952,731 | 41,978,930 | 26,200 |
ENST00000612133.4 | hg19 | chr17 | 41,952,731 | 41,985,310 | 32,580 |
ENST00000622681.4 | hg19 | chr17 | 41,952,731 | 41,987,079 | 34,349 |
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