MMD monocyte to macrophage differentiation associated
Information
- Symbol
- MMD
- Type
- protein-coding
- Description
- monocyte to macrophage differentiation associated
- Entrez Gene ID
- 23531
- Genome
- hg19
- Position
- chr17:53,469,983-53,499,196
- Genome
- hg38
- Position
- chr17:55,392,622-55,421,835
- MIM
- 604467 OMIM
- HGNC
- HGNC:7153 HGNC
- Ensembl
- ENSG00000108960 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 2 |
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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12 |
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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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Filtering | : |
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 | MMA |
SYNONYM | MMD1 |
SYNONYM | PAQR11 |
MIM | 604467 OMIM |
HGNC | HGNC:7153 HGNC |
Ensembl | ENSG00000108960 Ensembl |
AllianceGenome | HGNC:7153 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000262065.8 | hg38 | chr17 | 55,392,622 | 55,421,835 | 29,214 |
ENST00000649377.1 | hg38 | chr17 | 55,392,643 | 55,421,835 | 29,193 |
ENST00000262065.8 | hg19 | chr17 | 53,469,983 | 53,499,196 | 29,214 |
ENST00000649377.1 | hg19 | chr17 | 53,470,004 | 53,499,196 | 29,193 |
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