GMNC geminin coiled-coil domain containing
Information
- Symbol
- GMNC
- Type
- protein-coding
- Description
- geminin coiled-coil domain containing
- Entrez Gene ID
- 647309
- Genome
- hg19
- Position
- chr3:190,570,526-190,580,483
- Genome
- hg38
- Position
- chr3:190,852,737-190,862,694
- MIM
- 614448 OMIM
- HGNC
- HGNC:40049 HGNC
- Ensembl
- ENSG00000205835 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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42 |
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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 | GEMC1 |
MIM | 614448 OMIM |
HGNC | HGNC:40049 HGNC |
Ensembl | ENSG00000205835 Ensembl |
AllianceGenome | HGNC:40049 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000442080.6 | hg38 | chr3 | 190,852,737 | 190,862,694 | 9,958 |
ENST00000442080.6 | hg19 | chr3 | 190,570,526 | 190,580,483 | 9,958 |
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