KRR1 KRR1 small subunit processome component homolog
Information
- Symbol
- KRR1
- Type
- protein-coding
- Description
- KRR1 small subunit processome component homolog
- Entrez Gene ID
- 11103
- Genome
- hg19
- Position
- chr12:75,884,643-75,905,389
- Genome
- hg38
- Position
- chr12:75,490,863-75,511,609
- MIM
- 612817 OMIM
- HGNC
- HGNC:5176 HGNC
- Ensembl
- ENSG00000111615 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 6 |
Uncertain significance | 0 | 46 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
56 |
![]() |
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 | HRB2 |
SYNONYM | RIP-1 |
MIM | 612817 OMIM |
HGNC | HGNC:5176 HGNC |
Ensembl | ENSG00000111615 Ensembl |
AllianceGenome | HGNC:5176 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000229214.9 | hg38 | chr12 | 75,490,863 | 75,511,609 | 20,747 |
ENST00000438169.6 | hg38 | chr12 | 75,499,809 | 75,511,597 | 11,789 |
ENST00000229214.9 | hg19 | chr12 | 75,884,643 | 75,905,389 | 20,747 |
ENST00000438169.6 | hg19 | chr12 | 75,893,589 | 75,905,377 | 11,789 |
Genome browser