CRISP3 cysteine rich secretory protein 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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26 |
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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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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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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 | Aeg2 |
SYNONYM | CRISP-3 |
SYNONYM | CRS3 |
SYNONYM | SGP28 |
SYNONYM | dJ442L6.3 |
MIM | 618062 OMIM |
HGNC | HGNC:16904 HGNC |
Ensembl | ENSG00000096006 Ensembl |
AllianceGenome | HGNC:16904 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000371159.8 | hg38 | chr6 | 49,728,708 | 49,744,386 | 15,679 |
ENST00000263045.9 | hg38 | chr6 | 49,727,376 | 49,744,388 | 17,013 |
ENST00000433368.6 | hg38 | chr6 | 49,727,402 | 49,744,437 | 17,036 |
ENST00000263045.9 | hg19 | chr6 | 49,695,089 | 49,712,101 | 17,013 |
ENST00000433368.6 | hg19 | chr6 | 49,695,115 | 49,712,150 | 17,036 |
ENST00000371159.8 | hg19 | chr6 | 49,696,421 | 49,712,099 | 15,679 |
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