CATIP ciliogenesis associated TTC17 interacting protein
Information
- Symbol
- CATIP
- Type
- protein-coding
- Description
- ciliogenesis associated TTC17 interacting protein
- Entrez Gene ID
- 375307
- Genome
- hg19
- Position
- chr2:219,221,580-219,232,817
- Genome
- hg38
- Position
- chr2:218,356,857-218,368,094
- MIM
- 619387 OMIM
- HGNC
- HGNC:25062 HGNC
- Ensembl
- ENSG00000158428 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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42 |
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2 |
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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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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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 |
---|---|
SYNONYM | C2orf62 |
MIM | 619387 OMIM |
HGNC | HGNC:25062 HGNC |
Ensembl | ENSG00000158428 Ensembl |
AllianceGenome | HGNC:25062 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000289388.4 | hg38 | chr2 | 218,356,857 | 218,368,094 | 11,238 |
ENST00000289388.4 | hg19 | chr2 | 219,221,580 | 219,232,817 | 11,238 |
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