MIF4GD MIF4G domain containing
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 26 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
26 |
 |
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 | AD023 |
| SYNONYM | MIFD |
| SYNONYM | SLIP1 |
| MIM | 612072 OMIM |
| HGNC | HGNC:24030 HGNC |
| Ensembl | ENSG00000125457 Ensembl |
| AllianceGenome | HGNC:24030 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000579119.5 | hg38 | chr17 | 75,266,672 | 75,270,227 | 3,556 |
| ENST00000649805.1 | hg38 | chr17 | 75,266,512 | 75,271,211 | 4,700 |
| ENST00000245551.9 | hg38 | chr17 | 75,266,233 | 75,271,173 | 4,941 |
| ENST00000580571.5 | hg38 | chr17 | 75,266,435 | 75,271,227 | 4,793 |
| ENST00000579297.5 | hg38 | chr17 | 75,266,247 | 75,271,227 | 4,981 |
| ENST00000618645.5 | hg38 | chr17 | 75,266,283 | 75,270,414 | 4,132 |
| ENST00000581777.2 | hg38 | chr17 | 75,266,228 | 75,270,755 | 4,528 |
| ENST00000578305.5 | hg38 | chr17 | 75,266,681 | 75,271,200 | 4,520 |
| ENST00000325102.13 | hg38 | chr17 | 75,266,228 | 75,271,231 | 5,004 |
| ENST00000577542.5 | hg38 | chr17 | 75,266,264 | 75,271,155 | 4,892 |
| ENST00000581777.2 | hg19 | chr17 | 73,262,309 | 73,266,836 | 4,528 |
| ENST00000325102.13 | hg19 | chr17 | 73,262,309 | 73,267,312 | 5,004 |
| ENST00000245551.9 | hg19 | chr17 | 73,262,314 | 73,267,254 | 4,941 |
| ENST00000579297.5 | hg19 | chr17 | 73,262,328 | 73,267,308 | 4,981 |
| ENST00000577542.5 | hg19 | chr17 | 73,262,345 | 73,267,236 | 4,892 |
| ENST00000618645.5 | hg19 | chr17 | 73,262,364 | 73,266,495 | 4,132 |
| ENST00000580571.5 | hg19 | chr17 | 73,262,516 | 73,267,308 | 4,793 |
| ENST00000649805.1 | hg19 | chr17 | 73,262,593 | 73,267,292 | 4,700 |
| ENST00000579119.5 | hg19 | chr17 | 73,262,753 | 73,266,308 | 3,556 |
| ENST00000578305.5 | hg19 | chr17 | 73,262,762 | 73,267,281 | 4,520 |
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