TMEM185A transmembrane protein 185A
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| not provided | 6 | 0 |
| Uncertain significance | 0 | 8 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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10 |
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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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| 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 | CXorf13 |
| SYNONYM | FAM11A |
| SYNONYM | FRAXF |
| SYNONYM | ee3 |
| MIM | 300031 OMIM |
| HGNC | HGNC:17125 HGNC |
| Ensembl | ENSG00000269556 Ensembl |
| AllianceGenome | HGNC:17125 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000507237.5 | hg38 | chrX | 149,603,709 | 149,631,698 | 27,990 |
| ENST00000611119.4 | hg38 | chrX | 149,596,557 | 149,631,912 | 35,356 |
| ENST00000600449.8 | hg38 | chrX | 149,596,556 | 149,631,792 | 35,237 |
| ENST00000600449.8 | hg19 | chrX | 148,678,216 | 148,713,448 | 35,233 |
| ENST00000611119.4 | hg19 | chrX | 148,678,217 | 148,713,568 | 35,352 |
| ENST00000507237.5 | hg19 | chrX | 148,685,375 | 148,713,381 | 28,007 |
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