GRIP1 glutamate receptor interacting protein 1
Information
- Symbol
- GRIP1
- Type
- protein-coding
- Description
- glutamate receptor interacting protein 1
- Entrez Gene ID
- 23426
- Genome
- hg19
- Position
- chr12:66,741,211-67,072,856
- Genome
- hg38
- Position
- chr12:66,347,431-66,679,076
- MIM
- 604597 OMIM
- HGNC
- HGNC:18708 HGNC
- Ensembl
- ENSG00000155974 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 20 |
| Likely pathogenic | 0 | 16 |
| Benign | 0 | 54 |
| Likely benign | 0 | 918 |
| Conflicting classifications of pathogenicity | 0 | 48 |
| not provided | 5 | 0 |
| Uncertain significance | 0 | 264 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
112 |
 |
1,126 |
 |
10 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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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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| Category | : |
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| 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 | : |
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| 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 | FRASRS3 |
| SYNONYM | GRIP |
| MIM | 604597 OMIM |
| HGNC | HGNC:18708 HGNC |
| Ensembl | ENSG00000155974 Ensembl |
| AllianceGenome | HGNC:18708 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000359742.9 | hg38 | chr12 | 66,347,431 | 66,679,076 | 331,646 |
| ENST00000696989.1 | hg38 | chr12 | 66,347,663 | 66,646,372 | 298,710 |
| ENST00000398016.7 | hg38 | chr12 | 66,347,431 | 66,678,973 | 331,543 |
| ENST00000359742.9 | hg19 | chr12 | 66,741,211 | 67,072,856 | 331,646 |
| ENST00000398016.7 | hg19 | chr12 | 66,741,211 | 67,072,753 | 331,543 |
| ENST00000696989.1 | hg19 | chr12 | 66,741,443 | 67,040,152 | 298,710 |
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