TMEM139 transmembrane protein 139
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 24 |
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 |
---|---|
MIM | 616524 OMIM |
HGNC | HGNC:22058 HGNC |
Ensembl | ENSG00000178826 Ensembl |
AllianceGenome | HGNC:22058 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409541.5 | hg38 | chr7 | 143,284,954 | 143,288,047 | 3,094 |
ENST00000409244.5 | hg38 | chr7 | 143,284,951 | 143,287,296 | 2,346 |
ENST00000359333.8 | hg38 | chr7 | 143,284,958 | 143,288,048 | 3,091 |
ENST00000409102.5 | hg38 | chr7 | 143,279,957 | 143,287,296 | 7,340 |
ENST00000410004.1 | hg38 | chr7 | 143,284,957 | 143,288,048 | 3,092 |
ENST00000409102.5 | hg19 | chr7 | 142,977,050 | 142,984,389 | 7,340 |
ENST00000409244.5 | hg19 | chr7 | 142,982,044 | 142,984,389 | 2,346 |
ENST00000409541.5 | hg19 | chr7 | 142,982,047 | 142,985,140 | 3,094 |
ENST00000410004.1 | hg19 | chr7 | 142,982,050 | 142,985,141 | 3,092 |
ENST00000359333.8 | hg19 | chr7 | 142,982,051 | 142,985,141 | 3,091 |
Genome browser