SMIM10L2B small integral membrane protein 10 like 2B
Information
- Symbol
- SMIM10L2B
- Type
- protein-coding
- Description
- small integral membrane protein 10 like 2B
- Entrez Gene ID
- 644596
- Genome
- hg19
- Position
- chrX:134,229,015-134,232,742
- Genome
- hg38
- Position
- chrX:135,094,985-135,098,712
- HGNC
- HGNC:34500 HGNC
- Ensembl
- ENSG00000196972 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| not provided | 6 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
2 |
 |
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
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| 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
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| 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 | : |
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| 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 | LINC00086 |
| SYNONYM | LINC00087 |
| SYNONYM | NCRNA00086 |
| SYNONYM | NCRNA00087 |
| SYNONYM | SMIM10L2A |
| HGNC | HGNC:34500 HGNC |
| Ensembl | ENSG00000196972 Ensembl |
| AllianceGenome | HGNC:34500 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000433425.4 | hg38 | chrX | 135,094,985 | 135,098,712 | 3,728 |
| ENST00000433425.4 | hg19 | chrX | 134,229,015 | 134,232,742 | 3,728 |
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