SLC35F2 solute carrier family 35 member F2
Information
- Symbol
- SLC35F2
- Type
- protein-coding
- Description
- solute carrier family 35 member F2
- Entrez Gene ID
- 54733
- Genome
- hg19
- Position
- chr11:107,661,717-107,729,513
- Genome
- hg38
- Position
- chr11:107,790,991-107,858,787
- MIM
- 620350 OMIM
- HGNC
- HGNC:23615 HGNC
- Ensembl
- ENSG00000110660 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 26 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
26 |
 |
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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| 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 | HSNOV1 |
| MIM | 620350 OMIM |
| HGNC | HGNC:23615 HGNC |
| Ensembl | ENSG00000110660 Ensembl |
| AllianceGenome | HGNC:23615 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000525815.6 | hg38 | chr11 | 107,790,991 | 107,858,787 | 67,797 |
| ENST00000525071.5 | hg38 | chr11 | 107,790,991 | 107,928,293 | 137,303 |
| ENST00000375682.8 | hg38 | chr11 | 107,792,615 | 107,858,561 | 65,947 |
| ENST00000525815.6 | hg19 | chr11 | 107,661,717 | 107,729,513 | 67,797 |
| ENST00000525071.5 | hg19 | chr11 | 107,661,717 | 107,799,019 | 137,303 |
| ENST00000375682.8 | hg19 | chr11 | 107,663,341 | 107,729,287 | 65,947 |
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