HMGN3 high mobility group nucleosomal binding domain 3
Information
- Symbol
- HMGN3
- Type
- protein-coding
- Description
- high mobility group nucleosomal binding domain 3
- Entrez Gene ID
- 9324
- Genome
- hg19
- Position
- chr6:79,910,962-79,944,399
- Genome
- hg38
- Position
- chr6:79,201,245-79,234,682
- MIM
- 604502 OMIM
- HGNC
- HGNC:12312 HGNC
- Ensembl
- ENSG00000118418 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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14 |
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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 |
Search Word
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 | : | |
Filtering | : |
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 |
---|---|
SYNONYM | PNAS-24 |
SYNONYM | PNAS-25 |
SYNONYM | TRIP7 |
MIM | 604502 OMIM |
HGNC | HGNC:12312 HGNC |
Ensembl | ENSG00000118418 Ensembl |
AllianceGenome | HGNC:12312 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000706660.1 | hg38 | chr6 | 79,201,479 | 79,234,675 | 33,197 |
ENST00000703810.2 | hg38 | chr6 | 79,201,245 | 79,234,614 | 33,370 |
ENST00000275036.11 | hg38 | chr6 | 79,201,245 | 79,234,689 | 33,445 |
ENST00000706657.1 | hg38 | chr6 | 79,201,245 | 79,234,682 | 33,438 |
ENST00000706659.1 | hg38 | chr6 | 79,201,253 | 79,234,656 | 33,404 |
ENST00000620514.2 | hg38 | chr6 | 79,201,245 | 79,234,682 | 33,438 |
ENST00000344726.10 | hg38 | chr6 | 79,201,245 | 79,234,682 | 33,438 |
ENST00000703810.2 | hg19 | chr6 | 79,910,962 | 79,944,331 | 33,370 |
ENST00000344726.10 | hg19 | chr6 | 79,910,962 | 79,944,399 | 33,438 |
ENST00000620514.2 | hg19 | chr6 | 79,910,962 | 79,944,399 | 33,438 |
ENST00000706657.1 | hg19 | chr6 | 79,910,962 | 79,944,399 | 33,438 |
ENST00000275036.11 | hg19 | chr6 | 79,910,962 | 79,944,406 | 33,445 |
ENST00000706659.1 | hg19 | chr6 | 79,910,970 | 79,944,373 | 33,404 |
ENST00000706660.1 | hg19 | chr6 | 79,911,196 | 79,944,392 | 33,197 |
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