SLC37A2 solute carrier family 37 member 2
Information
- Symbol
- SLC37A2
- Type
- protein-coding
- Description
- solute carrier family 37 member 2
- Entrez Gene ID
- 219855
- Genome
- hg19
- Position
- chr11:124,933,232-124,959,131
- Genome
- hg38
- Position
- chr11:125,063,336-125,089,235
- MIM
- 619136 OMIM
- HGNC
- HGNC:20644 HGNC
- Ensembl
- ENSG00000134955 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 60 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
68 |
 |
2 |
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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| 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 | SPX2 |
| SYNONYM | pp11662 |
| MIM | 619136 OMIM |
| HGNC | HGNC:20644 HGNC |
| Ensembl | ENSG00000134955 Ensembl |
| AllianceGenome | HGNC:20644 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000308074.4 | hg38 | chr11 | 125,063,336 | 125,089,235 | 25,900 |
| ENST00000403796.7 | hg38 | chr11 | 125,063,305 | 125,090,516 | 27,212 |
| ENST00000403796.7 | hg19 | chr11 | 124,933,201 | 124,960,412 | 27,212 |
| ENST00000308074.4 | hg19 | chr11 | 124,933,232 | 124,959,131 | 25,900 |
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