CNIH2 cornichon family AMPA receptor auxiliary protein 2
Information
- Symbol
- CNIH2
- Type
- protein-coding
- Description
- cornichon family AMPA receptor auxiliary protein 2
- Entrez Gene ID
- 254263
- Genome
- hg19
- Position
- chr11:66,045,646-66,051,677
- Genome
- hg38
- Position
- chr11:66,278,175-66,284,206
- MIM
- 611288 OMIM
- HGNC
- HGNC:28744 HGNC
- Ensembl
- ENSG00000174871 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Uncertain significance | 0 | 6 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
8 |
 |
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
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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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| 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 | CNIH-2 |
| SYNONYM | Cnil |
| MIM | 611288 OMIM |
| HGNC | HGNC:28744 HGNC |
| Ensembl | ENSG00000174871 Ensembl |
| AllianceGenome | HGNC:28744 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000528852.5 | hg38 | chr11 | 66,278,190 | 66,284,193 | 6,004 |
| ENST00000311445.7 | hg38 | chr11 | 66,278,175 | 66,284,206 | 6,032 |
| ENST00000311445.7 | hg19 | chr11 | 66,045,646 | 66,051,677 | 6,032 |
| ENST00000528852.5 | hg19 | chr11 | 66,045,661 | 66,051,664 | 6,004 |
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