ANAPC5 anaphase promoting complex subunit 5
Information
- Symbol
- ANAPC5
- Type
- protein-coding
- Description
- anaphase promoting complex subunit 5
- Entrez Gene ID
- 51433
- Genome
- hg19
- Position
- chr12:121,746,048-121,790,214
- Genome
- hg38
- Position
- chr12:121,308,245-121,352,411
- MIM
- 606948 OMIM
- HGNC
- HGNC:15713 HGNC
- Ensembl
- ENSG00000089053 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 40 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
44 |
 |
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 | APC5 |
| MIM | 606948 OMIM |
| HGNC | HGNC:15713 HGNC |
| Ensembl | ENSG00000089053 Ensembl |
| AllianceGenome | HGNC:15713 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000541887.5 | hg38 | chr12 | 121,308,357 | 121,352,388 | 44,032 |
| ENST00000535482.1 | hg38 | chr12 | 121,308,358 | 121,331,391 | 23,034 |
| ENST00000441917.6 | hg38 | chr12 | 121,308,357 | 121,347,883 | 39,527 |
| ENST00000261819.8 | hg38 | chr12 | 121,308,245 | 121,352,411 | 44,167 |
| ENST00000261819.8 | hg19 | chr12 | 121,746,048 | 121,790,214 | 44,167 |
| ENST00000441917.6 | hg19 | chr12 | 121,746,160 | 121,785,686 | 39,527 |
| ENST00000535482.1 | hg19 | chr12 | 121,746,161 | 121,769,194 | 23,034 |
| ENST00000541887.5 | hg19 | chr12 | 121,746,160 | 121,790,191 | 44,032 |
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