GIMAP4 GTPase, IMAP family member 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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46 |
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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 | IAN-1 |
SYNONYM | IAN1 |
SYNONYM | IMAP4 |
SYNONYM | MSTP062 |
MIM | 608087 OMIM |
HGNC | HGNC:21872 HGNC |
Ensembl | ENSG00000133574 Ensembl |
AllianceGenome | HGNC:21872 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000255945.4 | hg38 | chr7 | 150,567,390 | 150,573,953 | 6,564 |
ENST00000461940.5 | hg38 | chr7 | 150,567,369 | 150,573,514 | 6,146 |
ENST00000461940.5 | hg19 | chr7 | 150,264,457 | 150,270,602 | 6,146 |
ENST00000255945.4 | hg19 | chr7 | 150,264,478 | 150,271,041 | 6,564 |
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