RMDN3 regulator of microtubule dynamics 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 2 | 0 |
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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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
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 |
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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 | FAM82A2 |
SYNONYM | FAM82C |
SYNONYM | RMD-3 |
SYNONYM | RMD3 |
SYNONYM | ptpip51 |
MIM | 611873 OMIM |
HGNC | HGNC:25550 HGNC |
Ensembl | ENSG00000137824 Ensembl |
AllianceGenome | HGNC:25550 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000260385.10 | hg38 | chr15 | 40,735,884 | 40,755,851 | 19,968 |
ENST00000338376.8 | hg38 | chr15 | 40,735,887 | 40,755,254 | 19,368 |
ENST00000260385.10 | hg19 | chr15 | 41,028,082 | 41,048,049 | 19,968 |
ENST00000338376.8 | hg19 | chr15 | 41,028,085 | 41,047,452 | 19,368 |
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