MOSPD2 motile sperm domain containing 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
not provided | 7 | 0 |
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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24 |
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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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Category | : |
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Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 |
---|---|
MIM | 301086 OMIM |
HGNC | HGNC:28381 HGNC |
Ensembl | ENSG00000130150 Ensembl |
AllianceGenome | HGNC:28381 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000482354.5 | hg38 | chrX | 14,873,455 | 14,921,756 | 48,302 |
ENST00000380492.8 | hg38 | chrX | 14,873,421 | 14,922,327 | 48,907 |
ENST00000497603.2 | hg38 | chrX | 14,873,529 | 14,874,454 | 926 |
ENST00000380492.8 | hg19 | chrX | 14,891,543 | 14,940,449 | 48,907 |
ENST00000482354.5 | hg19 | chrX | 14,891,577 | 14,939,878 | 48,302 |
ENST00000497603.2 | hg19 | chrX | 14,891,651 | 14,892,576 | 926 |
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