EIF3K eukaryotic translation initiation factor 3 subunit K
Information
- Symbol
- EIF3K
- Type
- protein-coding
- Description
- eukaryotic translation initiation factor 3 subunit K
- Entrez Gene ID
- 27335
- Genome
- hg19
- Position
- chr19:39,109,828-39,127,594
- Genome
- hg38
- Position
- chr19:38,619,188-38,636,954
- MIM
- 609596 OMIM
- HGNC
- HGNC:24656 HGNC
- Ensembl
- ENSG00000178982 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 | ARG134 |
SYNONYM | EIF3-p28 |
SYNONYM | EIF3S12 |
SYNONYM | HSPC029 |
SYNONYM | M9 |
SYNONYM | MSTP001 |
SYNONYM | PLAC-24 |
SYNONYM | PLAC24 |
SYNONYM | PRO1474 |
SYNONYM | PTD001 |
MIM | 609596 OMIM |
HGNC | HGNC:24656 HGNC |
Ensembl | ENSG00000178982 Ensembl |
AllianceGenome | HGNC:24656 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000592558.1 | hg38 | chr19 | 38,619,211 | 38,636,953 | 17,743 |
ENST00000545173.6 | hg38 | chr19 | 38,619,193 | 38,635,744 | 16,552 |
ENST00000593149.5 | hg38 | chr19 | 38,619,095 | 38,636,953 | 17,859 |
ENST00000538434.5 | hg38 | chr19 | 38,619,186 | 38,635,485 | 16,300 |
ENST00000588934.5 | hg38 | chr19 | 38,619,186 | 38,636,952 | 17,767 |
ENST00000614624.4 | hg38 | chr19 | 38,619,082 | 38,636,955 | 17,874 |
ENST00000248342.9 | hg38 | chr19 | 38,619,188 | 38,636,954 | 17,767 |
ENST00000614624.4 | hg19 | chr19 | 39,109,722 | 39,127,595 | 17,874 |
ENST00000593149.5 | hg19 | chr19 | 39,109,735 | 39,127,593 | 17,859 |
ENST00000538434.5 | hg19 | chr19 | 39,109,826 | 39,126,125 | 16,300 |
ENST00000588934.5 | hg19 | chr19 | 39,109,826 | 39,127,592 | 17,767 |
ENST00000248342.9 | hg19 | chr19 | 39,109,828 | 39,127,594 | 17,767 |
ENST00000545173.6 | hg19 | chr19 | 39,109,833 | 39,126,384 | 16,552 |
ENST00000592558.1 | hg19 | chr19 | 39,109,851 | 39,127,593 | 17,743 |
Genome browser