CRY2 cryptochrome circadian regulator 2
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Uncertain significance | 0 | 58 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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62 |
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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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| 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 | |||||||||||
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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 | HCRY2 |
| SYNONYM | PHLL2 |
| MIM | 603732 OMIM |
| HGNC | HGNC:2385 HGNC |
| Ensembl | ENSG00000121671 Ensembl |
| AllianceGenome | HGNC:2385 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000616623.4 | hg38 | chr11 | 45,847,406 | 45,883,248 | 35,843 |
| ENST00000616080.2 | hg38 | chr11 | 45,847,475 | 45,883,244 | 35,770 |
| ENST00000417225.6 | hg38 | chr11 | 45,847,118 | 45,881,233 | 34,116 |
| ENST00000443527.6 | hg38 | chr11 | 45,847,406 | 45,883,247 | 35,842 |
| ENST00000417225.6 | hg19 | chr11 | 45,868,669 | 45,902,784 | 34,116 |
| ENST00000443527.6 | hg19 | chr11 | 45,868,957 | 45,904,798 | 35,842 |
| ENST00000616623.4 | hg19 | chr11 | 45,868,957 | 45,904,799 | 35,843 |
| ENST00000616080.2 | hg19 | chr11 | 45,869,026 | 45,904,795 | 35,770 |
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