TMEM91 transmembrane protein 91
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 12 |
| Likely pathogenic | 0 | 18 |
| Benign | 0 | 40 |
| Likely benign | 0 | 100 |
| Conflicting classifications of pathogenicity | 0 | 2 |
| Uncertain significance | 0 | 178 |
Ranking
| ClinVar | |
|---|---|
![]() |
0 |
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0 |
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60 |
![]() |
268 |
![]() |
2 |
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
|
| 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 | DSPC3 |
| SYNONYM | IFITMD6 |
| SYNONYM | SynDIG3 |
| MIM | 618294 OMIM |
| HGNC | HGNC:32393 HGNC |
| Ensembl | ENSG00000142046 Ensembl |
| AllianceGenome | HGNC:32393 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000544232.5 | hg38 | chr19 | 41,376,740 | 41,384,083 | 7,344 |
| ENST00000539627.5 | hg38 | chr19 | 41,350,911 | 41,384,083 | 33,173 |
| ENST00000392002.7 | hg38 | chr19 | 41,376,533 | 41,384,083 | 7,551 |
| ENST00000542945.5 | hg38 | chr19 | 41,376,773 | 41,384,060 | 7,288 |
| ENST00000356385.8 | hg38 | chr19 | 41,377,292 | 41,384,083 | 6,792 |
| ENST00000436170.6 | hg38 | chr19 | 41,376,578 | 41,384,083 | 7,506 |
| ENST00000604123.5 | hg38 | chr19 | 41,354,169 | 41,384,083 | 29,915 |
| ENST00000447302.6 | hg38 | chr19 | 41,376,733 | 41,384,083 | 7,351 |
| ENST00000413014.6 | hg38 | chr19 | 41,364,056 | 41,384,083 | 20,028 |
| ENST00000539627.5 | hg19 | chr19 | 41,856,816 | 41,889,988 | 33,173 |
| ENST00000604123.5 | hg19 | chr19 | 41,860,074 | 41,889,988 | 29,915 |
| ENST00000413014.6 | hg19 | chr19 | 41,869,961 | 41,889,988 | 20,028 |
| ENST00000392002.7 | hg19 | chr19 | 41,882,438 | 41,889,988 | 7,551 |
| ENST00000436170.6 | hg19 | chr19 | 41,882,483 | 41,889,988 | 7,506 |
| ENST00000447302.6 | hg19 | chr19 | 41,882,638 | 41,889,988 | 7,351 |
| ENST00000544232.5 | hg19 | chr19 | 41,882,645 | 41,889,988 | 7,344 |
| ENST00000542945.5 | hg19 | chr19 | 41,882,678 | 41,889,965 | 7,288 |
| ENST00000356385.8 | hg19 | chr19 | 41,883,197 | 41,889,988 | 6,792 |
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