NIFK nucleolar protein interacting with the FHA domain of MKI67
Information
- Symbol
- NIFK
- Type
- protein-coding
- Description
- nucleolar protein interacting with the FHA domain of MKI67
- Entrez Gene ID
- 84365
- Genome
- hg19
- Position
- chr2:122,484,521-122,494,451
- Genome
- hg38
- Position
- chr2:121,726,945-121,736,875
- MIM
- 611970 OMIM
- HGNC
- HGNC:17838 HGNC
- Ensembl
- ENSG00000155438 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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32 |
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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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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | MKI67IP |
SYNONYM | Nopp34 |
MIM | 611970 OMIM |
HGNC | HGNC:17838 HGNC |
Ensembl | ENSG00000155438 Ensembl |
AllianceGenome | HGNC:17838 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000285814.9 | hg38 | chr2 | 121,726,945 | 121,736,875 | 9,931 |
ENST00000285814.9 | hg19 | chr2 | 122,484,521 | 122,494,451 | 9,931 |
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