MOB4 MOB family member 4, phocein
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 4 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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4 |
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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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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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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 | 2C4D |
SYNONYM | CGI-95 |
SYNONYM | MOB1 |
SYNONYM | MOB3 |
SYNONYM | MOBKL3 |
SYNONYM | PHOCN |
SYNONYM | PREI3 |
MIM | 609361 OMIM |
HGNC | HGNC:17261 HGNC |
Ensembl | ENSG00000115540 Ensembl |
AllianceGenome | HGNC:17261 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000233892.8 | hg38 | chr2 | 197,515,571 | 197,553,699 | 38,129 |
ENST00000409360.1 | hg38 | chr2 | 197,516,160 | 197,551,279 | 35,120 |
ENST00000323303.9 | hg38 | chr2 | 197,516,066 | 197,553,699 | 37,634 |
ENST00000448447.6 | hg38 | chr2 | 197,516,047 | 197,551,012 | 34,966 |
ENST00000409916.5 | hg38 | chr2 | 197,515,581 | 197,550,816 | 35,236 |
ENST00000233892.8 | hg19 | chr2 | 198,380,295 | 198,418,423 | 38,129 |
ENST00000409916.5 | hg19 | chr2 | 198,380,305 | 198,415,540 | 35,236 |
ENST00000448447.6 | hg19 | chr2 | 198,380,771 | 198,415,736 | 34,966 |
ENST00000323303.9 | hg19 | chr2 | 198,380,790 | 198,418,423 | 37,634 |
ENST00000409360.1 | hg19 | chr2 | 198,380,884 | 198,416,003 | 35,120 |
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