ALG10B ALG10 alpha-1,2-glucosyltransferase B
Information
- Symbol
- ALG10B
- Type
- protein-coding
- Description
- ALG10 alpha-1,2-glucosyltransferase B
- Entrez Gene ID
- 144245
- Genome
- hg19
- Position
- chr12:38,710,576-38,723,523
- Genome
- hg38
- Position
- chr12:38,316,774-38,329,721
- MIM
- 603313 OMIM
- HGNC
- HGNC:31088 HGNC
- Ensembl
- ENSG00000175548 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 8 |
| 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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| 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 | ALG10 |
| SYNONYM | KCR1 |
| MIM | 603313 OMIM |
| HGNC | HGNC:31088 HGNC |
| Ensembl | ENSG00000175548 Ensembl |
| AllianceGenome | HGNC:31088 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000551464.1 | hg38 | chr12 | 38,316,762 | 38,323,982 | 7,221 |
| ENST00000308742.9 | hg38 | chr12 | 38,316,774 | 38,329,721 | 12,948 |
| ENST00000551464.1 | hg19 | chr12 | 38,710,564 | 38,717,784 | 7,221 |
| ENST00000308742.9 | hg19 | chr12 | 38,710,576 | 38,723,523 | 12,948 |
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