GRIK4 glutamate ionotropic receptor kainate type subunit 4
Information
- Symbol
- GRIK4
- Type
- protein-coding
- Description
- glutamate ionotropic receptor kainate type subunit 4
- Entrez Gene ID
- 2900
- Genome
- hg19
- Position
- chr11:120,382,457-120,859,615
- Genome
- hg38
- Position
- chr11:120,511,748-120,988,906
- MIM
- 600282 OMIM
- HGNC
- HGNC:4582 HGNC
- Ensembl
- ENSG00000149403 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 26 |
| Likely benign | 0 | 20 |
| Uncertain significance | 0 | 106 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
152 |
 |
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
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| 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
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| 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
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| Category | : |
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| 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 | EAA1 |
| SYNONYM | GRIK |
| SYNONYM | GluK4 |
| SYNONYM | GluK4-2 |
| SYNONYM | KA1 |
| MIM | 600282 OMIM |
| HGNC | HGNC:4582 HGNC |
| Ensembl | ENSG00000149403 Ensembl |
| AllianceGenome | HGNC:4582 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000638419.1 | hg38 | chr11 | 120,511,746 | 120,986,685 | 474,940 |
| ENST00000527524.8 | hg38 | chr11 | 120,511,748 | 120,988,906 | 477,159 |
| ENST00000438375.2 | hg38 | chr11 | 120,564,434 | 120,987,261 | 422,828 |
| ENST00000638419.1 | hg19 | chr11 | 120,382,455 | 120,857,394 | 474,940 |
| ENST00000527524.8 | hg19 | chr11 | 120,382,457 | 120,859,615 | 477,159 |
| ENST00000438375.2 | hg19 | chr11 | 120,435,143 | 120,857,970 | 422,828 |
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