TSPY1 testis specific protein Y-linked 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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2 |
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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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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 | CT78 |
SYNONYM | DYS14 |
SYNONYM | TSPY |
SYNONYM | pJA923 |
MIM | 480100 OMIM |
HGNC | HGNC:12381 HGNC |
Ensembl | ENSG00000258992 Ensembl |
AllianceGenome | HGNC:12381 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000451548.6 | hg38 | chrY | 9,466,955 | 9,469,749 | 2,795 |
ENST00000423647.6 | hg38 | chrY | 9,466,955 | 9,469,748 | 2,794 |
ENST00000423647.6 | hg19 | chrY | 9,304,564 | 9,307,357 | 2,794 |
ENST00000451548.6 | hg19 | chrY | 9,304,564 | 9,307,358 | 2,795 |
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