SLC41A2 solute carrier family 41 member 2
Information
- Symbol
- SLC41A2
- Type
- protein-coding
- Description
- solute carrier family 41 member 2
- Entrez Gene ID
- 84102
- Genome
- hg19
- Position
- chr12:105,195,579-105,352,068
- Genome
- hg38
- Position
- chr12:104,801,801-104,958,290
- MIM
- 610802 OMIM
- HGNC
- HGNC:31045 HGNC
- Ensembl
- ENSG00000136052 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 36 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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90 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | SLC41A1-L1 |
MIM | 610802 OMIM |
HGNC | HGNC:31045 HGNC |
Ensembl | ENSG00000136052 Ensembl |
AllianceGenome | HGNC:31045 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000258538.8 | hg38 | chr12 | 104,801,801 | 104,958,290 | 156,490 |
ENST00000258538.8 | hg19 | chr12 | 105,195,579 | 105,352,068 | 156,490 |
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