PIM2 Pim-2 proto-oncogene, serine/threonine kinase
Information
- Symbol
- PIM2
- Type
- protein-coding
- Description
- Pim-2 proto-oncogene, serine/threonine kinase
- Entrez Gene ID
- 11040
- Genome
- hg19
- Position
- chrX:48,770,459-48,776,301
- Genome
- hg38
- Position
- chrX:48,913,182-48,919,024
- MIM
- 300295 OMIM
- HGNC
- HGNC:8987 HGNC
- Ensembl
- ENSG00000102096 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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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
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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000710360.1 | hg38 | chrX | 48,913,182 | 48,919,024 | 5,843 |
ENST00000376509.4 | hg38 | chrX | 48,913,182 | 48,919,024 | 5,843 |
ENST00000376509.4 | hg19 | chrX | 48,770,459 | 48,776,301 | 5,843 |
ENST00000710360.1 | hg19 | chrX | 48,770,459 | 48,776,301 | 5,843 |
Key | Value |
---|---|
strand | - |
UniProt | OG |
start | 48,770,458 |
Gene Symbol | PIM2 |
Entrez GeneId | 11,040 |
Chr Band | Xp11.23 |
end | 48,776,412 |
chr | chrX |
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