GALNT9 polypeptide N-acetylgalactosaminyltransferase 9
Information
- Symbol
- GALNT9
- Type
- protein-coding
- Description
- polypeptide N-acetylgalactosaminyltransferase 9
- Entrez Gene ID
- 50614
- Genome
- hg19
- Position
- chr12:132,680,924-132,690,573
- Genome
- hg38
- Position
- chr12:132,196,372-132,329,589
- MIM
- 606251 OMIM
- HGNC
- HGNC:4131 HGNC
- Ensembl
- ENSG00000182870 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 12 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
18 |
 |
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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| 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 | GALNAC-T9 |
| SYNONYM | GALNACT9 |
| MIM | 606251 OMIM |
| HGNC | HGNC:4131 HGNC |
| Ensembl | ENSG00000182870 Ensembl |
| AllianceGenome | HGNC:4131 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000397325.6 | hg38 | chr12 | 132,196,372 | 132,206,028 | 9,657 |
| ENST00000541995.5 | hg38 | chr12 | 132,197,073 | 132,205,792 | 8,720 |
| ENST00000328957.13 | hg38 | chr12 | 132,196,372 | 132,329,589 | 133,218 |
| ENST00000397325.2 | hg19 | chr12 | 132,680,924 | 132,690,573 | 9,650 |
| ENST00000328957.8 | hg19 | chr12 | 132,681,054 | 132,905,789 | 224,736 |
| ENST00000535228.1 | hg19 | chr12 | 132,681,054 | 132,834,281 | 153,228 |
| ENST00000541995.1 | hg19 | chr12 | 132,681,618 | 132,690,337 | 8,720 |
| ENST00000535208.1 | hg19 | chr12 | 132,834,390 | 132,851,804 | 17,415 |
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