BRME1 break repair meiotic recombinase recruitment factor 1
Information
- Symbol
- BRME1
- Type
- protein-coding
- Description
- break repair meiotic recombinase recruitment factor 1
- Entrez Gene ID
- 79173
- Genome
- hg19
- Position
- chr19:13,993,161-14,016,930
- Genome
- hg38
- Position
- chr19:13,882,348-13,906,117
- MIM
- 619276 OMIM
- HGNC
- HGNC:28153 HGNC
- Ensembl
- ENSG00000132016 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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18 |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | C19orf57 |
SYNONYM | MEIOK21 |
MIM | 619276 OMIM |
HGNC | HGNC:28153 HGNC |
Ensembl | ENSG00000132016 Ensembl |
AllianceGenome | HGNC:28153 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000346736.6 | hg38 | chr19 | 13,882,355 | 13,906,165 | 23,811 |
ENST00000591586.5 | hg38 | chr19 | 13,882,389 | 13,906,107 | 23,719 |
ENST00000586783.6 | hg38 | chr19 | 13,882,348 | 13,906,117 | 23,770 |
ENST00000586783.6 | hg19 | chr19 | 13,993,161 | 14,016,930 | 23,770 |
ENST00000346736.6 | hg19 | chr19 | 13,993,168 | 14,016,978 | 23,811 |
ENST00000591586.5 | hg19 | chr19 | 13,993,202 | 14,016,920 | 23,719 |
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