KXD1 KxDL motif containing 1
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 0 | 2 |
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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20 |
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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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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 | BORCS4 |
SYNONYM | C10orf50 |
SYNONYM | C19orf50 |
SYNONYM | KXDL |
SYNONYM | MST096 |
SYNONYM | MSTP096 |
MIM | 615178 OMIM |
HGNC | HGNC:28420 HGNC |
Ensembl | ENSG00000105700 Ensembl |
AllianceGenome | HGNC:28420 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000599319.5 | hg38 | chr19 | 18,558,539 | 18,568,720 | 10,182 |
ENST00000599000.5 | hg38 | chr19 | 18,557,879 | 18,567,318 | 9,440 |
ENST00000595073.5 | hg38 | chr19 | 18,557,888 | 18,569,297 | 11,410 |
ENST00000602094.5 | hg38 | chr19 | 18,559,112 | 18,569,378 | 10,267 |
ENST00000539106.5 | hg38 | chr19 | 18,557,762 | 18,569,387 | 11,626 |
ENST00000601630.5 | hg38 | chr19 | 18,557,876 | 18,569,310 | 11,435 |
ENST00000540691.5 | hg38 | chr19 | 18,557,762 | 18,569,387 | 11,626 |
ENST00000222307.9 | hg38 | chr19 | 18,557,870 | 18,569,378 | 11,509 |
ENST00000598830.5 | hg38 | chr19 | 18,561,520 | 18,567,272 | 5,753 |
ENST00000540691.5 | hg19 | chr19 | 18,668,572 | 18,680,197 | 11,626 |
ENST00000539106.5 | hg19 | chr19 | 18,668,572 | 18,680,197 | 11,626 |
ENST00000222307.9 | hg19 | chr19 | 18,668,680 | 18,680,188 | 11,509 |
ENST00000598830.5 | hg19 | chr19 | 18,672,330 | 18,678,082 | 5,753 |
ENST00000599000.5 | hg19 | chr19 | 18,668,689 | 18,678,128 | 9,440 |
ENST00000595073.5 | hg19 | chr19 | 18,668,698 | 18,680,107 | 11,410 |
ENST00000599319.5 | hg19 | chr19 | 18,669,349 | 18,679,530 | 10,182 |
ENST00000601630.5 | hg19 | chr19 | 18,668,686 | 18,680,120 | 11,435 |
ENST00000602094.5 | hg19 | chr19 | 18,669,922 | 18,680,188 | 10,267 |
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