CILP2 cartilage intermediate layer protein 2
Information
- Symbol
- CILP2
- Type
- protein-coding
- Description
- cartilage intermediate layer protein 2
- Entrez Gene ID
- 148113
- Genome
- hg19
- Position
- chr19:19,649,074-19,657,468
- Genome
- hg38
- Position
- chr19:19,538,265-19,546,659
- MIM
- 612419 OMIM
- HGNC
- HGNC:24213 HGNC
- Ensembl
- ENSG00000160161 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 174 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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184 |
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CLIP-2 |
MIM | 612419 OMIM |
HGNC | HGNC:24213 HGNC |
Ensembl | ENSG00000160161 Ensembl |
AllianceGenome | HGNC:24213 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000291495.5 | hg38 | chr19 | 19,538,265 | 19,546,659 | 8,395 |
ENST00000586018.5 | hg38 | chr19 | 19,538,248 | 19,546,659 | 8,412 |
ENST00000586018.5 | hg19 | chr19 | 19,649,057 | 19,657,468 | 8,412 |
ENST00000291495.5 | hg19 | chr19 | 19,649,074 | 19,657,468 | 8,395 |
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