SIDT2 SID1 transmembrane family member 2
Information
- Symbol
- SIDT2
- Type
- protein-coding
- Description
- SID1 transmembrane family member 2
- Entrez Gene ID
- 51092
- Genome
- hg19
- Position
- chr11:117,049,459-117,068,158
- Genome
- hg38
- Position
- chr11:117,178,743-117,197,442
- MIM
- 617551 OMIM
- HGNC
- HGNC:24272 HGNC
- Ensembl
- ENSG00000149577 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 8 |
| Uncertain significance | 0 | 62 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
76 |
 |
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
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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
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| 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 | CGI-40 |
| MIM | 617551 OMIM |
| HGNC | HGNC:24272 HGNC |
| Ensembl | ENSG00000149577 Ensembl |
| AllianceGenome | HGNC:24272 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000431081.6 | hg38 | chr11 | 117,179,223 | 117,197,445 | 18,223 |
| ENST00000324225.9 | hg38 | chr11 | 117,178,743 | 117,197,442 | 18,700 |
| ENST00000532062.1 | hg38 | chr11 | 117,192,617 | 117,197,279 | 4,663 |
| ENST00000628876.2 | hg38 | chr11 | 117,179,223 | 117,195,984 | 16,762 |
| ENST00000324225.9 | hg19 | chr11 | 117,049,459 | 117,068,158 | 18,700 |
| ENST00000431081.6 | hg19 | chr11 | 117,049,939 | 117,068,161 | 18,223 |
| ENST00000628876.2 | hg19 | chr11 | 117,049,939 | 117,066,700 | 16,762 |
| ENST00000532062.1 | hg19 | chr11 | 117,063,333 | 117,067,995 | 4,663 |
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