TGOLN2 trans-golgi network protein 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 62 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
64 |
![]() |
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 | TGN38 |
SYNONYM | TGN46 |
SYNONYM | TGN48 |
SYNONYM | TGN51 |
SYNONYM | TTGN2 |
SYNONYM | hTGN46 |
SYNONYM | hTGN48 |
SYNONYM | hTGN51 |
MIM | 603062 OMIM |
HGNC | HGNC:15450 HGNC |
Ensembl | ENSG00000152291 Ensembl |
AllianceGenome | HGNC:15450 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000444342.2 | hg38 | chr2 | 85,324,385 | 85,327,985 | 3,601 |
ENST00000398263.6 | hg38 | chr2 | 85,318,027 | 85,328,251 | 10,225 |
ENST00000409015.5 | hg38 | chr2 | 85,321,894 | 85,328,024 | 6,131 |
ENST00000409232.7 | hg38 | chr2 | 85,321,894 | 85,328,024 | 6,131 |
ENST00000377386.8 | hg38 | chr2 | 85,318,027 | 85,327,989 | 9,963 |
ENST00000377386.8 | hg19 | chr2 | 85,545,150 | 85,555,112 | 9,963 |
ENST00000398263.6 | hg19 | chr2 | 85,545,150 | 85,555,374 | 10,225 |
ENST00000409015.5 | hg19 | chr2 | 85,549,017 | 85,555,147 | 6,131 |
ENST00000409232.7 | hg19 | chr2 | 85,549,017 | 85,555,147 | 6,131 |
ENST00000444342.2 | hg19 | chr2 | 85,551,508 | 85,555,108 | 3,601 |
Genome browser