RPAP3 RNA polymerase II associated protein 3
Information
- Symbol
- RPAP3
- Type
- protein-coding
- Description
- RNA polymerase II associated protein 3
- Entrez Gene ID
- 79657
- Genome
- hg19
- Position
- chr12:48,055,032-48,099,813
- Genome
- hg38
- Position
- chr12:47,661,249-47,706,030
- MIM
- 611477 OMIM
- HGNC
- HGNC:26151 HGNC
- Ensembl
- ENSG00000005175 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 64 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
70 |
![]() |
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 | Tah1 |
SYNONYM | hSpagh |
MIM | 611477 OMIM |
HGNC | HGNC:26151 HGNC |
Ensembl | ENSG00000005175 Ensembl |
AllianceGenome | HGNC:26151 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000380650.4 | hg38 | chr12 | 47,663,293 | 47,705,986 | 42,694 |
ENST00000005386.8 | hg38 | chr12 | 47,661,249 | 47,706,030 | 44,782 |
ENST00000432584.7 | hg38 | chr12 | 47,663,292 | 47,706,026 | 42,735 |
ENST00000005386.8 | hg19 | chr12 | 48,055,032 | 48,099,813 | 44,782 |
ENST00000432584.7 | hg19 | chr12 | 48,057,075 | 48,099,809 | 42,735 |
ENST00000380650.4 | hg19 | chr12 | 48,057,076 | 48,099,769 | 42,694 |
Genome browser