MOG myelin oligodendrocyte glycoprotein
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 2 |
| Benign | 0 | 8 |
| Likely benign | 0 | 6 |
| not provided | 5 | 0 |
| Uncertain significance | 0 | 22 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
34 |
 |
4 |
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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| 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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| 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 | BTN6 |
| SYNONYM | BTNL11 |
| SYNONYM | MOGIG2 |
| SYNONYM | NRCLP7 |
| MIM | 159465 OMIM |
| HGNC | HGNC:7197 HGNC |
| Ensembl | ENSG00000204655 Ensembl |
| AllianceGenome | HGNC:7197 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000376888.6 | hg38 | chr6 | 29,657,003 | 29,672,111 | 15,109 |
| ENST00000416766.6 | hg38 | chr6 | 29,657,210 | 29,671,185 | 13,976 |
| ENST00000494692.5 | hg38 | chr6 | 29,657,210 | 29,671,718 | 14,509 |
| ENST00000376891.8 | hg38 | chr6 | 29,657,210 | 29,671,718 | 14,509 |
| ENST00000376894.8 | hg38 | chr6 | 29,657,092 | 29,672,372 | 15,281 |
| ENST00000376898.7 | hg38 | chr6 | 29,657,210 | 29,671,718 | 14,509 |
| ENST00000483013.5 | hg38 | chr6 | 29,657,210 | 29,671,185 | 13,976 |
| ENST00000490427.5 | hg38 | chr6 | 29,657,210 | 29,671,185 | 13,976 |
| ENST00000431798.6 | hg38 | chr6 | 29,657,210 | 29,672,372 | 15,163 |
| ENST00000376917.8 | hg38 | chr6 | 29,657,092 | 29,672,365 | 15,274 |
| ENST00000396704.7 | hg38 | chr6 | 29,657,210 | 29,671,185 | 13,976 |
| ENST00000396701.6 | hg38 | chr6 | 29,657,210 | 29,671,718 | 14,509 |
| ENST00000376888.6 | hg19 | chr6 | 29,624,780 | 29,639,888 | 15,109 |
| ENST00000376891.8 | hg19 | chr6 | 29,624,987 | 29,639,495 | 14,509 |
| ENST00000494692.5 | hg19 | chr6 | 29,624,987 | 29,639,495 | 14,509 |
| ENST00000396701.6 | hg19 | chr6 | 29,624,987 | 29,639,495 | 14,509 |
| ENST00000376898.7 | hg19 | chr6 | 29,624,987 | 29,639,495 | 14,509 |
| ENST00000376894.8 | hg19 | chr6 | 29,624,869 | 29,640,149 | 15,281 |
| ENST00000376917.8 | hg19 | chr6 | 29,624,869 | 29,640,142 | 15,274 |
| ENST00000490427.5 | hg19 | chr6 | 29,624,987 | 29,638,962 | 13,976 |
| ENST00000483013.5 | hg19 | chr6 | 29,624,987 | 29,638,962 | 13,976 |
| ENST00000416766.6 | hg19 | chr6 | 29,624,987 | 29,638,962 | 13,976 |
| ENST00000396704.7 | hg19 | chr6 | 29,624,987 | 29,638,962 | 13,976 |
| ENST00000431798.6 | hg19 | chr6 | 29,624,987 | 29,640,149 | 15,163 |
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