TMEM101 transmembrane protein 101
Information
- Symbol
- TMEM101
- Type
- protein-coding
- Description
- transmembrane protein 101
- Entrez Gene ID
- 84336
- Genome
- hg19
- Position
- chr17:42,088,556-42,100,519
- Genome
- hg38
- Position
- chr17:44,011,188-44,023,151
- HGNC
- HGNC:28653 HGNC
- Ensembl
- ENSG00000091947 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 26 |
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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000206380.8 | hg38 | chr17 | 44,011,188 | 44,014,963 | 3,776 |
ENST00000587529.1 | hg38 | chr17 | 44,012,509 | 44,014,952 | 2,444 |
ENST00000589334.5 | hg38 | chr17 | 44,011,188 | 44,023,151 | 11,964 |
ENST00000206380.8 | hg19 | chr17 | 42,088,556 | 42,092,331 | 3,776 |
ENST00000589334.5 | hg19 | chr17 | 42,088,556 | 42,100,519 | 11,964 |
ENST00000587529.1 | hg19 | chr17 | 42,089,877 | 42,092,320 | 2,444 |
Genome browser