MFSD2B MFSD2 lysolipid transporter B, sphingolipid
Information
- Symbol
- MFSD2B
- Type
- protein-coding
- Description
- MFSD2 lysolipid transporter B, sphingolipid
- Entrez Gene ID
- 388931
- Genome
- hg19
- Position
- chr2:24,232,955-24,249,645
- Genome
- hg38
- Position
- chr2:24,010,085-24,026,775
- MIM
- 617845 OMIM
- HGNC
- HGNC:37207 HGNC
- Ensembl
- ENSG00000205639 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 2 | 0 |
| Uncertain significance | 0 | 72 |
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
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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 | SLC59A2 |
| MIM | 617845 OMIM |
| HGNC | HGNC:37207 HGNC |
| Ensembl | ENSG00000205639 Ensembl |
| AllianceGenome | HGNC:37207 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000338315.6 | hg38 | chr2 | 24,010,085 | 24,026,775 | 16,691 |
| ENST00000669179.1 | hg38 | chr2 | 24,010,081 | 24,026,775 | 16,695 |
| ENST00000406420.7 | hg38 | chr2 | 24,010,081 | 24,024,293 | 14,213 |
| ENST00000406420.7 | hg19 | chr2 | 24,232,951 | 24,247,163 | 14,213 |
| ENST00000669179.1 | hg19 | chr2 | 24,232,951 | 24,249,645 | 16,695 |
| ENST00000338315.6 | hg19 | chr2 | 24,232,955 | 24,249,645 | 16,691 |
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