APMAP adipocyte plasma membrane associated protein
Information
- Symbol
- APMAP
- Type
- protein-coding
- Description
- adipocyte plasma membrane associated protein
- Entrez Gene ID
- 57136
- Genome
- hg19
- Position
- chr20:24,943,561-24,973,387
- Genome
- hg38
- Position
- chr20:24,962,925-24,992,751
- MIM
- 615884 OMIM
- HGNC
- HGNC:13238 HGNC
- Ensembl
- ENSG00000101474 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 60 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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60 |
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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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| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | BSCv |
| SYNONYM | C20orf3 |
| MIM | 615884 OMIM |
| HGNC | HGNC:13238 HGNC |
| Ensembl | ENSG00000101474 Ensembl |
| AllianceGenome | HGNC:13238 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000217456.3 | hg38 | chr20 | 24,962,925 | 24,992,751 | 29,827 |
| ENST00000217456.3 | hg19 | chr20 | 24,943,561 | 24,973,387 | 29,827 |
| Key | Value |
|---|---|
| strand | - |
| start | 24,943,579 |
| Gene Symbol | APMAP |
| Entrez GeneId | 57,136 |
| Chr Band | 20p11.2 |
| end | 24,973,424 |
| chr | chr20 |
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