CRCP CGRP receptor component
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 14 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
14 |
 |
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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| 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 | C17 |
| SYNONYM | CGRP-RCP |
| SYNONYM | CGRPRCP |
| SYNONYM | POLR3I |
| SYNONYM | POLR3J |
| SYNONYM | RCP |
| SYNONYM | RCP9 |
| SYNONYM | RPC9 |
| MIM | 606121 OMIM |
| HGNC | HGNC:17888 HGNC |
| Ensembl | ENSG00000241258 Ensembl |
| AllianceGenome | HGNC:17888 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000431089.6 | hg38 | chr7 | 66,114,826 | 66,152,870 | 38,045 |
| ENST00000398684.6 | hg38 | chr7 | 66,114,841 | 66,152,511 | 37,671 |
| ENST00000338592.5 | hg38 | chr7 | 66,114,850 | 66,153,289 | 38,440 |
| ENST00000395326.8 | hg38 | chr7 | 66,114,847 | 66,154,568 | 39,722 |
| ENST00000431089.6 | hg19 | chr7 | 65,579,813 | 65,617,857 | 38,045 |
| ENST00000398684.6 | hg19 | chr7 | 65,579,828 | 65,617,498 | 37,671 |
| ENST00000395326.8 | hg19 | chr7 | 65,579,834 | 65,619,555 | 39,722 |
| ENST00000338592.5 | hg19 | chr7 | 65,579,837 | 65,618,276 | 38,440 |
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