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Gene Report
| Basic information | Functional annotation | Related other genetic factors | ADD to My Gene Set | Comment on Gene | View All Comments on Gene |
| Approved Symbol | FBXW4P1 |
|---|---|
| Previous Symbol | FBXW3, SHFM3P1 |
| Symbol Alias | FBW3 |
| Approved Name | F-box and WD repeat domain containing 4 pseudogene 1 |
| Previous Name | F-box and WD-40 domain protein 3, "split hand/foot malformation (ectrodactyly) type 3 pseudogene 1" |
| Location | 22q11 |
| Position | chr22:23262767-23265005, 1 |
| External Links |
HGNC: 13609 Entrez Gene: 26226 Ensembl: ENSG00000230701 UCSC: uc010gty.5 |
| No. of Studies | 0. Gene is from "Mapped by Literature SNP " |
Gene functional annotation
Gene related GO terms (count: 0)
Gene related KEGG pathways (count: 0)
Gene related BioCarta pathways (count: 0)
Gene related interactors from protein-protein interactions data in HPRD (count: 0)
Related other genetic factors
Gene related SNPs (count: 6)
Literature-origin SNPs (count: 1)
LD-proxies (count: 5)
Gene related CNVs (count: 0)
Gene related other variants (count: 0)
Gene related regions (count: 0)
View in gBrowse
Region: chr22:23262767..23265005 View in gBrowse
