KDM4D lysine demethylase 4D
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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58 |
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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
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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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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 | JMJD2D |
MIM | 609766 OMIM |
HGNC | HGNC:25498 HGNC |
Ensembl | ENSG00000186280 Ensembl |
AllianceGenome | HGNC:25498 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000610872.1 | hg38 | chr11 | 94,997,173 | 94,999,363 | 2,191 |
ENST00000536741.1 | hg38 | chr11 | 94,973,823 | 94,999,514 | 25,692 |
ENST00000335080.6 | hg38 | chr11 | 94,973,709 | 94,999,519 | 25,811 |
ENST00000335080.6 | hg19 | chr11 | 94,706,873 | 94,732,683 | 25,811 |
ENST00000536741.1 | hg19 | chr11 | 94,706,987 | 94,732,678 | 25,692 |
ENST00000610872.1 | hg19 | chr11 | 94,730,337 | 94,732,527 | 2,191 |
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