CSRP2 cysteine and glycine rich protein 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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14 |
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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
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CRP2 |
SYNONYM | LMO5 |
SYNONYM | SmLIM |
MIM | 601871 OMIM |
HGNC | HGNC:2470 HGNC |
Ensembl | ENSG00000175183 Ensembl |
AllianceGenome | HGNC:2470 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000546966.5 | hg38 | chr12 | 76,858,842 | 76,879,023 | 20,182 |
ENST00000311083.10 | hg38 | chr12 | 76,858,709 | 76,879,019 | 20,311 |
ENST00000552330.5 | hg38 | chr12 | 76,858,829 | 76,878,991 | 20,163 |
ENST00000547435.1 | hg38 | chr12 | 76,859,469 | 76,878,985 | 19,517 |
ENST00000311083.10 | hg19 | chr12 | 77,252,489 | 77,272,799 | 20,311 |
ENST00000552330.5 | hg19 | chr12 | 77,252,609 | 77,272,771 | 20,163 |
ENST00000546966.5 | hg19 | chr12 | 77,252,622 | 77,272,803 | 20,182 |
ENST00000547435.1 | hg19 | chr12 | 77,253,249 | 77,272,765 | 19,517 |
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