MORN2 MORN repeat containing 2
Information
- Symbol
- MORN2
- Type
- protein-coding
- Description
- MORN repeat containing 2
- Entrez Gene ID
- 729967
- Genome
- hg19
- Position
- chr2:39,103,117-39,109,850
- Genome
- hg38
- Position
- chr2:38,875,976-38,882,709
- HGNC
- HGNC:30166 HGNC
- Ensembl
- ENSG00000188010 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 6 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
6 |
 |
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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| 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 | BLOCK27 |
| SYNONYM | MOPT |
| HGNC | HGNC:30166 HGNC |
| Ensembl | ENSG00000188010 Ensembl |
| AllianceGenome | HGNC:30166 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000409131.2 | hg38 | chr2 | 38,876,068 | 38,882,652 | 6,585 |
| ENST00000644631.4 | hg38 | chr2 | 38,875,976 | 38,882,709 | 6,734 |
| ENST00000410014.5 | hg38 | chr2 | 38,875,991 | 38,882,646 | 6,656 |
| ENST00000409077.2 | hg38 | chr2 | 38,876,038 | 38,882,697 | 6,660 |
| ENST00000409665.5 | hg38 | chr2 | 38,876,011 | 38,882,647 | 6,637 |
| ENST00000644631.4 | hg19 | chr2 | 39,103,117 | 39,109,850 | 6,734 |
| ENST00000410014.5 | hg19 | chr2 | 39,103,132 | 39,109,787 | 6,656 |
| ENST00000409665.5 | hg19 | chr2 | 39,103,152 | 39,109,788 | 6,637 |
| ENST00000409077.2 | hg19 | chr2 | 39,103,179 | 39,109,838 | 6,660 |
| ENST00000409131.2 | hg19 | chr2 | 39,103,209 | 39,109,793 | 6,585 |
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