MON2 MON2 homolog, regulator of endosome-to-Golgi trafficking
Information
- Symbol
- MON2
- Type
- protein-coding
- Description
- MON2 homolog, regulator of endosome-to-Golgi trafficking
- Entrez Gene ID
- 23041
- Genome
- hg19
- Position
- chr12:62,860,606-62,994,256
- Genome
- hg38
- Position
- chr12:62,466,826-62,600,476
- MIM
- 616822 OMIM
- HGNC
- HGNC:29177 HGNC
- Ensembl
- ENSG00000061987 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 8 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 104 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
112 |
 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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
|
| 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 |
|---|---|
| MIM | 616822 OMIM |
| HGNC | HGNC:29177 HGNC |
| Ensembl | ENSG00000061987 Ensembl |
| AllianceGenome | HGNC:29177 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000546600.5 | hg38 | chr12 | 62,466,822 | 62,593,278 | 126,457 |
| ENST00000393630.8 | hg38 | chr12 | 62,466,826 | 62,600,476 | 133,651 |
| ENST00000552115.5 | hg38 | chr12 | 62,466,849 | 62,553,365 | 86,517 |
| ENST00000393629.6 | hg38 | chr12 | 62,466,848 | 62,592,865 | 126,018 |
| ENST00000641654.1 | hg38 | chr12 | 62,466,817 | 62,597,583 | 130,767 |
| ENST00000552738.5 | hg38 | chr12 | 62,466,848 | 62,592,865 | 126,018 |
| ENST00000641654.1 | hg19 | chr12 | 62,860,597 | 62,991,363 | 130,767 |
| ENST00000546600.5 | hg19 | chr12 | 62,860,602 | 62,987,058 | 126,457 |
| ENST00000393630.8 | hg19 | chr12 | 62,860,606 | 62,994,256 | 133,651 |
| ENST00000552738.5 | hg19 | chr12 | 62,860,628 | 62,986,645 | 126,018 |
| ENST00000393629.6 | hg19 | chr12 | 62,860,628 | 62,986,645 | 126,018 |
| ENST00000552115.5 | hg19 | chr12 | 62,860,629 | 62,947,145 | 86,517 |
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