TMEM205 transmembrane protein 205
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 28 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
28 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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 | : |
|
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 | UNQ501 |
MIM | 613771 OMIM |
HGNC | HGNC:29631 HGNC |
Ensembl | ENSG00000105518 Ensembl |
AllianceGenome | HGNC:29631 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000589555.5 | hg38 | chr19 | 11,342,779 | 11,346,271 | 3,493 |
ENST00000586218.5 | hg38 | chr19 | 11,342,776 | 11,346,210 | 3,435 |
ENST00000587948.5 | hg38 | chr19 | 11,342,779 | 11,346,406 | 3,628 |
ENST00000586956.5 | hg38 | chr19 | 11,342,778 | 11,346,285 | 3,508 |
ENST00000586590.5 | hg38 | chr19 | 11,342,778 | 11,346,268 | 3,491 |
ENST00000354882.10 | hg38 | chr19 | 11,342,778 | 11,346,268 | 3,491 |
ENST00000588560.5 | hg38 | chr19 | 11,342,785 | 11,346,248 | 3,464 |
ENST00000447337.5 | hg38 | chr19 | 11,342,776 | 11,346,305 | 3,530 |
ENST00000593256.6 | hg38 | chr19 | 11,342,776 | 11,346,300 | 3,525 |
ENST00000586218.5 | hg19 | chr19 | 11,453,452 | 11,456,886 | 3,435 |
ENST00000593256.6 | hg19 | chr19 | 11,453,452 | 11,456,976 | 3,525 |
ENST00000447337.5 | hg19 | chr19 | 11,453,452 | 11,456,981 | 3,530 |
ENST00000354882.10 | hg19 | chr19 | 11,453,454 | 11,456,944 | 3,491 |
ENST00000586590.5 | hg19 | chr19 | 11,453,454 | 11,456,944 | 3,491 |
ENST00000586956.5 | hg19 | chr19 | 11,453,454 | 11,456,961 | 3,508 |
ENST00000589555.5 | hg19 | chr19 | 11,453,455 | 11,456,947 | 3,493 |
ENST00000587948.5 | hg19 | chr19 | 11,453,455 | 11,457,082 | 3,628 |
ENST00000588560.5 | hg19 | chr19 | 11,453,461 | 11,456,924 | 3,464 |
Genome browser