MCM6 minichromosome maintenance complex component 6
Information
- Symbol
- MCM6
- Type
- protein-coding
- Description
- minichromosome maintenance complex component 6
- Entrez Gene ID
- 4175
- Genome
- hg19
- Position
- chr2:136,597,196-136,634,013
- Genome
- hg38
- Position
- chr2:135,839,626-135,876,443
- MIM
- 601806 OMIM
- HGNC
- HGNC:6949 HGNC
- Ensembl
- ENSG00000076003 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 16 |
| Likely benign | 0 | 22 |
| association | 0 | 10 |
| Uncertain significance | 0 | 86 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
4 |
 |
116 |
 |
12 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | MCG40308 |
| SYNONYM | Mis5 |
| SYNONYM | P105MCM |
| MIM | 601806 OMIM |
| HGNC | HGNC:6949 HGNC |
| Ensembl | ENSG00000076003 Ensembl |
| AllianceGenome | HGNC:6949 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000264156.3 | hg38 | chr2 | 135,839,626 | 135,876,443 | 36,818 |
| ENST00000264156.3 | hg19 | chr2 | 136,597,196 | 136,634,013 | 36,818 |
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