FHIP1B FHF complex subunit HOOK interacting protein 1B
Information
- Symbol
- FHIP1B
- Type
- protein-coding
- Description
- FHF complex subunit HOOK interacting protein 1B
- Entrez Gene ID
- 84067
- Genome
- hg19
- Position
- chr11:6,232,575-6,255,941
- Genome
- hg38
- Position
- chr11:6,211,345-6,234,711
- MIM
- 620229 OMIM
- HGNC
- HGNC:25378 HGNC
- Ensembl
- ENSG00000051009 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 8 |
| Uncertain significance | 0 | 122 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
130 |
 |
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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| 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 | C11orf56 |
| SYNONYM | FAM160A2 |
| SYNONYM | FHIP |
| MIM | 620229 OMIM |
| HGNC | HGNC:25378 HGNC |
| Ensembl | ENSG00000051009 Ensembl |
| AllianceGenome | HGNC:25378 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000449352.7 | hg38 | chr11 | 6,211,345 | 6,234,636 | 23,292 |
| ENST00000524416.1 | hg38 | chr11 | 6,216,570 | 6,234,663 | 18,094 |
| ENST00000265978.8 | hg38 | chr11 | 6,211,345 | 6,234,711 | 23,367 |
| ENST00000449352.7 | hg19 | chr11 | 6,232,575 | 6,255,866 | 23,292 |
| ENST00000265978.8 | hg19 | chr11 | 6,232,575 | 6,255,941 | 23,367 |
| ENST00000524416.1 | hg19 | chr11 | 6,237,800 | 6,255,893 | 18,094 |
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