MOSPD1 motile sperm domain containing 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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12 |
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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 |
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 | : | |
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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 | DJ473B4 |
MIM | 300674 OMIM |
HGNC | HGNC:25235 HGNC |
Ensembl | ENSG00000101928 Ensembl |
AllianceGenome | HGNC:25235 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000370783.8 | hg38 | chrX | 134,887,632 | 134,915,257 | 27,626 |
ENST00000370777.1 | hg38 | chrX | 134,889,123 | 134,899,534 | 10,412 |
ENST00000370779.8 | hg38 | chrX | 134,889,015 | 134,915,227 | 26,213 |
ENST00000370783.8 | hg19 | chrX | 134,021,662 | 134,049,287 | 27,626 |
ENST00000370779.8 | hg19 | chrX | 134,023,045 | 134,049,257 | 26,213 |
ENST00000370777.1 | hg19 | chrX | 134,023,153 | 134,033,564 | 10,412 |
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