MAGIX MAGI family member, X-linked
Information
- Symbol
- MAGIX
- Type
- protein-coding
- Description
- MAGI family member, X-linked
- Entrez Gene ID
- 79917
- Genome
- hg19
- Position
- chrX:49,020,121-49,025,111
- Genome
- hg38
- Position
- chrX:49,162,758-49,168,774
- HGNC
- HGNC:30006 HGNC
- Ensembl
- ENSG00000269313 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 31 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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33 |
![]() |
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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| 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 | JM10 |
| SYNONYM | PDZX |
| HGNC | HGNC:30006 HGNC |
| Ensembl | ENSG00000269313 Ensembl |
| AllianceGenome | HGNC:30006 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000614074.4 | hg38 | chrX | 49,162,874 | 49,166,399 | 3,526 |
| ENST00000616266.4 | hg38 | chrX | 49,162,564 | 49,168,483 | 5,920 |
| ENST00000615915.4 | hg38 | chrX | 49,163,932 | 49,166,632 | 2,701 |
| ENST00000595224.6 | hg38 | chrX | 49,162,758 | 49,168,774 | 6,017 |
| ENST00000615626.4 | hg38 | chrX | 49,162,843 | 49,166,632 | 3,790 |
| ENST00000616266.4 | hg19 | chrX | 49,020,121 | 49,024,820 | 4,700 |
| ENST00000595224.6 | hg19 | chrX | 49,020,121 | 49,025,111 | 4,991 |
| ENST00000614074.4 | hg19 | chrX | 49,020,121 | 49,022,738 | 2,618 |
| ENST00000615626.4 | hg19 | chrX | 49,020,121 | 49,022,971 | 2,851 |
| ENST00000615915.4 | hg19 | chrX | 49,020,270 | 49,022,971 | 2,702 |
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