METTL21A methyltransferase 21A, HSPA lysine
Information
- Symbol
- METTL21A
- Type
- protein-coding
- Description
- methyltransferase 21A, HSPA lysine
- Entrez Gene ID
- 151194
- Genome
- hg19
- Position
- chr2:208,477,447-208,489,275
- Genome
- hg38
- Position
- chr2:207,612,723-207,624,551
- MIM
- 615257 OMIM
- HGNC
- HGNC:30476 HGNC
- Ensembl
- ENSG00000144401 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Uncertain significance | 0 | 20 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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22 |
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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 |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | FAM119A |
SYNONYM | HCA557b |
SYNONYM | HSPA-KMT |
MIM | 615257 OMIM |
HGNC | HGNC:30476 HGNC |
Ensembl | ENSG00000144401 Ensembl |
AllianceGenome | HGNC:30476 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000458426.5 | hg38 | chr2 | 207,581,353 | 207,625,331 | 43,979 |
ENST00000448007.6 | hg38 | chr2 | 207,612,104 | 207,624,983 | 12,880 |
ENST00000426075.5 | hg38 | chr2 | 207,612,843 | 207,624,566 | 11,724 |
ENST00000406927.6 | hg38 | chr2 | 207,612,743 | 207,625,378 | 12,636 |
ENST00000411432.6 | hg38 | chr2 | 207,612,739 | 207,625,394 | 12,656 |
ENST00000425132.5 | hg38 | chr2 | 207,581,695 | 207,625,379 | 43,685 |
ENST00000448823.2 | hg38 | chr2 | 207,612,727 | 207,624,380 | 11,654 |
ENST00000432416.5 | hg38 | chr2 | 207,580,631 | 207,625,121 | 44,491 |
ENST00000272839.7 | hg38 | chr2 | 207,612,723 | 207,624,551 | 11,829 |
ENST00000442521.1 | hg38 | chr2 | 207,612,980 | 207,625,927 | 12,948 |
ENST00000432416.5 | hg19 | chr2 | 208,445,355 | 208,489,845 | 44,491 |
ENST00000458426.5 | hg19 | chr2 | 208,446,077 | 208,490,055 | 43,979 |
ENST00000425132.5 | hg19 | chr2 | 208,446,419 | 208,490,103 | 43,685 |
ENST00000448007.6 | hg19 | chr2 | 208,476,828 | 208,489,707 | 12,880 |
ENST00000272839.7 | hg19 | chr2 | 208,477,447 | 208,489,275 | 11,829 |
ENST00000448823.2 | hg19 | chr2 | 208,477,451 | 208,489,104 | 11,654 |
ENST00000411432.6 | hg19 | chr2 | 208,477,463 | 208,490,118 | 12,656 |
ENST00000406927.6 | hg19 | chr2 | 208,477,467 | 208,490,102 | 12,636 |
ENST00000426075.5 | hg19 | chr2 | 208,477,567 | 208,489,290 | 11,724 |
ENST00000442521.1 | hg19 | chr2 | 208,477,704 | 208,490,651 | 12,948 |
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