MINAR1 membrane integral NOTCH2 associated receptor 1
Information
- Symbol
- MINAR1
- Type
- protein-coding
- Description
- membrane integral NOTCH2 associated receptor 1
- Entrez Gene ID
- 23251
- Genome
- hg19
- Position
- chr15:79,724,678-79,764,646
- Genome
- hg38
- Position
- chr15:79,432,336-79,472,304
- MIM
- 618054 OMIM
- HGNC
- HGNC:29172 HGNC
- Ensembl
- ENSG00000169330 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 8 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 132 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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142 |
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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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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 | KIAA1024 |
SYNONYM | UBTOR |
MIM | 618054 OMIM |
HGNC | HGNC:29172 HGNC |
Ensembl | ENSG00000169330 Ensembl |
AllianceGenome | HGNC:29172 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000305428.8 | hg38 | chr15 | 79,432,336 | 79,472,304 | 39,969 |
ENST00000305428.8 | hg19 | chr15 | 79,724,678 | 79,764,646 | 39,969 |
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