HOOK2 hook microtubule tethering protein 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 102 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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112 |
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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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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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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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MIM | 607824 OMIM |
SYNONYM | HK2 |
HGNC | HGNC:19885 HGNC |
Ensembl | ENSG00000095066 Ensembl |
AllianceGenome | HGNC:19885 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000397668.8 | hg38 | chr19 | 12,763,003 | 12,775,552 | 12,550 |
ENST00000264827.9 | hg38 | chr19 | 12,763,004 | 12,775,620 | 12,617 |
ENST00000397668.8 | hg19 | chr19 | 12,873,817 | 12,886,366 | 12,550 |
ENST00000264827.9 | hg19 | chr19 | 12,873,818 | 12,886,434 | 12,617 |
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