POU2F2 POU class 2 homeobox 2
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 1 | 0 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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42 |
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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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Category | : |
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Search word | : | |
Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 | OCT2 |
SYNONYM | OTF2 |
SYNONYM | Oct-2 |
MIM | 164176 OMIM |
HGNC | HGNC:9213 HGNC |
Ensembl | ENSG00000028277 Ensembl |
AllianceGenome | HGNC:9213 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000560558.5 | hg38 | chr19 | 42,089,553 | 42,132,419 | 42,867 |
ENST00000342301.8 | hg38 | chr19 | 42,089,353 | 42,132,476 | 43,124 |
ENST00000526816.6 | hg38 | chr19 | 42,089,790 | 42,132,427 | 42,638 |
ENST00000529067.5 | hg38 | chr19 | 42,090,205 | 42,132,465 | 42,261 |
ENST00000389341.9 | hg38 | chr19 | 42,086,110 | 42,132,478 | 46,369 |
ENST00000560398.5 | hg38 | chr19 | 42,091,230 | 42,132,419 | 41,190 |
ENST00000529952.5 | hg38 | chr19 | 42,091,815 | 42,132,473 | 40,659 |
ENST00000692977.1 | hg38 | chr19 | 42,086,110 | 42,132,446 | 46,337 |
ENST00000625670.2 | hg38 | chr19 | 42,110,706 | 42,132,428 | 21,723 |
ENST00000389341.9 | hg19 | chr19 | 42,590,262 | 42,636,630 | 46,369 |
ENST00000342301.8 | hg19 | chr19 | 42,593,505 | 42,636,628 | 43,124 |
ENST00000529952.5 | hg19 | chr19 | 42,595,967 | 42,636,625 | 40,659 |
ENST00000526816.6 | hg19 | chr19 | 42,593,942 | 42,636,579 | 42,638 |
ENST00000529067.5 | hg19 | chr19 | 42,594,357 | 42,636,617 | 42,261 |
ENST00000692977.1 | hg19 | chr19 | 42,590,262 | 42,636,598 | 46,337 |
ENST00000560398.5 | hg19 | chr19 | 42,595,382 | 42,636,571 | 41,190 |
ENST00000560558.5 | hg19 | chr19 | 42,593,705 | 42,636,571 | 42,867 |
ENST00000625670.2 | hg19 | chr19 | 42,614,858 | 42,636,580 | 21,723 |
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