CTXN2 cortexin 2
Information
- Symbol
- CTXN2
- Type
- protein-coding
- Description
- cortexin 2
- Entrez Gene ID
- 399697
- Genome
- hg19
- Position
- chr15:48,470,319-48,495,907
- Genome
- hg38
- Position
- chr15:48,178,122-48,203,710
- HGNC
- HGNC:31109 HGNC
- Ensembl
- ENSG00000233932 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 16 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
18 |
 |
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
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||||||||||||||
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000644354.1 | hg38 | chr15 | 48,178,122 | 48,203,710 | 25,589 |
| ENST00000645050.1 | hg38 | chr15 | 48,178,467 | 48,203,697 | 25,231 |
| ENST00000647363.1 | hg38 | chr15 | 48,192,046 | 48,203,744 | 11,699 |
| ENST00000417307.3 | hg38 | chr15 | 48,191,665 | 48,203,758 | 12,094 |
| ENST00000644354.1 | hg19 | chr15 | 48,470,319 | 48,495,907 | 25,589 |
| ENST00000645050.1 | hg19 | chr15 | 48,470,664 | 48,495,894 | 25,231 |
| ENST00000417307.3 | hg19 | chr15 | 48,483,862 | 48,495,955 | 12,094 |
| ENST00000647363.1 | hg19 | chr15 | 48,484,243 | 48,495,941 | 11,699 |
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