RIMKLB ribosomal modification protein rimK like family member B
Information
- Symbol
- RIMKLB
- Type
- protein-coding
- Description
- ribosomal modification protein rimK like family member B
- Entrez Gene ID
- 57494
- Genome
- hg19
- Position
- chr12:8,852,442-8,929,786
- Genome
- hg38
- Position
- chr12:8,699,846-8,777,190
- MIM
- 614054 OMIM
- HGNC
- HGNC:29228 HGNC
- Ensembl
- ENSG00000166532 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 22 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
22 |
 |
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 | FAM80B |
| SYNONYM | NAAGS |
| SYNONYM | NAAGS-I |
| MIM | 614054 OMIM |
| HGNC | HGNC:29228 HGNC |
| Ensembl | ENSG00000166532 Ensembl |
| AllianceGenome | HGNC:29228 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000357529.7 | hg38 | chr12 | 8,697,922 | 8,777,191 | 79,270 |
| ENST00000619374.4 | hg38 | chr12 | 8,713,743 | 8,783,085 | 69,343 |
| ENST00000535829.6 | hg38 | chr12 | 8,697,991 | 8,777,191 | 79,201 |
| ENST00000538135.5 | hg38 | chr12 | 8,699,846 | 8,777,190 | 77,345 |
| ENST00000357529.7 | hg19 | chr12 | 8,850,518 | 8,929,787 | 79,270 |
| ENST00000535829.6 | hg19 | chr12 | 8,850,587 | 8,929,787 | 79,201 |
| ENST00000538135.5 | hg19 | chr12 | 8,852,442 | 8,929,786 | 77,345 |
| ENST00000619374.4 | hg19 | chr12 | 8,866,339 | 8,935,681 | 69,343 |
Genome browser