NCKIPSD NCK interacting protein with SH3 domain
Information
- Symbol
- NCKIPSD
- Type
- protein-coding
- Description
- NCK interacting protein with SH3 domain
- Entrez Gene ID
- 51517
- Genome
- hg19
- Position
- chr3:48,711,277-48,723,348
- Genome
- hg38
- Position
- chr3:48,673,844-48,685,915
- MIM
- 606671 OMIM
- HGNC
- HGNC:15486 HGNC
- Ensembl
- ENSG00000213672 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 84 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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96 |
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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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| 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
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| Category | : |
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| 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 | AF3P21 |
| SYNONYM | DIP |
| SYNONYM | DIP1 |
| SYNONYM | ORF1 |
| SYNONYM | SPIN90 |
| SYNONYM | VIP54 |
| SYNONYM | WASLBP |
| SYNONYM | WISH |
| MIM | 606671 OMIM |
| HGNC | HGNC:15486 HGNC |
| Ensembl | ENSG00000213672 Ensembl |
| AllianceGenome | HGNC:15486 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000294129.7 | hg38 | chr3 | 48,673,844 | 48,685,915 | 12,072 |
| ENST00000416649.6 | hg38 | chr3 | 48,673,844 | 48,685,884 | 12,041 |
| ENST00000416649.6 | hg19 | chr3 | 48,711,277 | 48,723,317 | 12,041 |
| ENST00000294129.7 | hg19 | chr3 | 48,711,277 | 48,723,348 | 12,072 |
| Key | Value |
|---|---|
| strand | - |
| UniProt | OG |
| start | 48,711,271 |
| Gene Symbol | NCKIPSD |
| Entrez GeneId | 51,517 |
| Chr Band | 3p21 |
| end | 48,723,365 |
| chr | chr3 |
| Name | NCK interacting protein with SH3 domain |
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