CSRP1 cysteine and glycine rich protein 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
34 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
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 | : |
|
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 | CRP |
SYNONYM | CRP1 |
SYNONYM | CSRP |
SYNONYM | CYRP |
SYNONYM | D1S181E |
SYNONYM | HEL-141 |
SYNONYM | HEL-S-286 |
MIM | 123876 OMIM |
HGNC | HGNC:2469 HGNC |
Ensembl | ENSG00000159176 Ensembl |
AllianceGenome | HGNC:2469 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000340006.7 | hg38 | chr1 | 201,483,530 | 201,507,123 | 23,594 |
ENST00000532460.5 | hg38 | chr1 | 201,483,979 | 201,496,573 | 12,595 |
ENST00000367306.5 | hg38 | chr1 | 201,483,530 | 201,509,456 | 25,927 |
ENST00000531916.5 | hg38 | chr1 | 201,483,926 | 201,509,456 | 25,531 |
ENST00000533432.5 | hg38 | chr1 | 201,484,363 | 201,506,839 | 22,477 |
ENST00000526256.5 | hg38 | chr1 | 201,484,240 | 201,507,123 | 22,884 |
ENST00000526723.5 | hg38 | chr1 | 201,484,677 | 201,507,123 | 22,447 |
ENST00000340006.7 | hg19 | chr1 | 201,452,658 | 201,476,251 | 23,594 |
ENST00000367306.5 | hg19 | chr1 | 201,452,658 | 201,478,584 | 25,927 |
ENST00000526256.5 | hg19 | chr1 | 201,453,368 | 201,476,251 | 22,884 |
ENST00000526723.5 | hg19 | chr1 | 201,453,805 | 201,476,251 | 22,447 |
ENST00000531916.5 | hg19 | chr1 | 201,453,054 | 201,478,584 | 25,531 |
ENST00000532460.5 | hg19 | chr1 | 201,453,107 | 201,465,701 | 12,595 |
ENST00000533432.5 | hg19 | chr1 | 201,453,491 | 201,475,967 | 22,477 |
Genome browser