SMCO2 single-pass membrane protein with coiled-coil domains 2
Information
- Symbol
- SMCO2
- Type
- protein-coding
- Description
- single-pass membrane protein with coiled-coil domains 2
- Entrez Gene ID
- 341346
- Genome
- hg19
- Position
- chr12:27,599,669-27,655,118
- Genome
- hg38
- Position
- chr12:27,446,736-27,502,185
- HGNC
- HGNC:34448 HGNC
- Ensembl
- ENSG00000165935 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
not provided | 1 | 0 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
48 |
![]() |
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
|
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 | C12orf70 |
HGNC | HGNC:34448 HGNC |
Ensembl | ENSG00000165935 Ensembl |
AllianceGenome | HGNC:34448 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000298876.8 | hg38 | chr12 | 27,466,810 | 27,502,185 | 35,376 |
ENST00000698358.1 | hg38 | chr12 | 27,446,745 | 27,502,185 | 55,441 |
ENST00000535986.2 | hg38 | chr12 | 27,446,736 | 27,502,185 | 55,450 |
ENST00000535986.2 | hg19 | chr12 | 27,599,669 | 27,655,118 | 55,450 |
ENST00000698358.1 | hg19 | chr12 | 27,599,678 | 27,655,118 | 55,441 |
ENST00000298876.8 | hg19 | chr12 | 27,619,743 | 27,655,118 | 35,376 |
Genome browser