MSANTD2 Myb/SANT DNA binding domain containing 2
Information
- Symbol
- MSANTD2
- Type
- protein-coding
- Description
- Myb/SANT DNA binding domain containing 2
- Entrez Gene ID
- 79684
- Genome
- hg19
- Position
- chr11:124,636,394-124,670,302
- Genome
- hg38
- Position
- chr11:124,766,498-124,800,406
- HGNC
- HGNC:26266 HGNC
- Ensembl
- ENSG00000120458 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 36 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
38 |
 |
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
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| 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
|
| Category | : |
|
| Search word | : | |
| 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 | : |
|
| 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 | C11orf61 |
| HGNC | HGNC:26266 HGNC |
| Ensembl | ENSG00000120458 Ensembl |
| AllianceGenome | HGNC:26266 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000374979.8 | hg38 | chr11 | 124,766,498 | 124,800,406 | 33,909 |
| ENST00000526629.1 | hg38 | chr11 | 124,766,528 | 124,776,242 | 9,715 |
| ENST00000239614.8 | hg38 | chr11 | 124,766,498 | 124,800,673 | 34,176 |
| ENST00000674284.1 | hg38 | chr11 | 124,766,498 | 124,800,706 | 34,209 |
| ENST00000524950.1 | hg38 | chr11 | 124,767,494 | 124,800,383 | 32,890 |
| ENST00000374979.8 | hg19 | chr11 | 124,636,394 | 124,670,302 | 33,909 |
| ENST00000239614.8 | hg19 | chr11 | 124,636,394 | 124,670,569 | 34,176 |
| ENST00000674284.1 | hg19 | chr11 | 124,636,394 | 124,670,602 | 34,209 |
| ENST00000526629.1 | hg19 | chr11 | 124,636,424 | 124,646,138 | 9,715 |
| ENST00000524950.1 | hg19 | chr11 | 124,637,390 | 124,670,279 | 32,890 |
Genome browser