AP1M2 adaptor related protein complex 1 subunit mu 2
Information
- Symbol
- AP1M2
- Type
- protein-coding
- Description
- adaptor related protein complex 1 subunit mu 2
- Entrez Gene ID
- 10053
- Genome
- hg19
- Position
- chr19:10,683,347-10,697,991
- Genome
- hg38
- Position
- chr19:10,572,671-10,587,315
- MIM
- 607309 OMIM
- HGNC
- HGNC:558 HGNC
- Ensembl
- ENSG00000129354 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 50 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
50 |
 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| 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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| Search word | : | |
| 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 | AP1-mu2 |
| SYNONYM | HSMU1B |
| SYNONYM | MU-1B |
| SYNONYM | MU1B |
| SYNONYM | mu2 |
| MIM | 607309 OMIM |
| HGNC | HGNC:558 HGNC |
| Ensembl | ENSG00000129354 Ensembl |
| AllianceGenome | HGNC:558 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000590923.5 | hg38 | chr19 | 10,572,671 | 10,587,315 | 14,645 |
| ENST00000250244.11 | hg38 | chr19 | 10,572,671 | 10,587,312 | 14,642 |
| ENST00000250244.11 | hg19 | chr19 | 10,683,347 | 10,697,988 | 14,642 |
| ENST00000590923.5 | hg19 | chr19 | 10,683,347 | 10,697,991 | 14,645 |
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