FREY1 Frey regulator of sperm-oocyte fusion 1
Information
- Symbol
- FREY1
- Type
- protein-coding
- Description
- Frey regulator of sperm-oocyte fusion 1
- Entrez Gene ID
- 143678
- Genome
- hg19
- Position
- chr11:45,928,085-45,928,822
- Genome
- hg38
- Position
- chr11:45,906,534-45,907,271
- HGNC
- HGNC:37213 HGNC
- Ensembl
- ENSG00000234776 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 4 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
6 |
 |
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
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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 |
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| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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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 | C11orf94 |
| SYNONYM | Frey |
| HGNC | HGNC:37213 HGNC |
| Ensembl | ENSG00000234776 Ensembl |
| AllianceGenome | HGNC:37213 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000449465.2 | hg38 | chr11 | 45,906,534 | 45,907,271 | 738 |
| ENST00000449465.2 | hg19 | chr11 | 45,928,085 | 45,928,822 | 738 |
| Key | Value |
|---|---|
| strand | - |
| start | 45,928,085 |
| Gene Symbol | C11orf94 |
| Entrez GeneId | 143,678 |
| Chr Band | 11p11.2 |
| end | 45,928,832 |
| chr | chr11 |
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