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This gene encodes a phosphatidylinositol 3-phosphate-binding protein that functions as a master conductor for aggregate clearance by autophagy. This protein shuttles from the nuclear membrane to colocalize with aggregated proteins, where it complexes with other autophagic components to achieve macroautophagy-mediated clearance of these aggregated proteins. However, it is not necessary for starvation-induced macroautophagy. [provided by RefSeq, May 2010]
WDFY3 (WD Repeat And FYVE Domain Containing 3) is a Protein Coding gene. Diseases associated with WDFY3 include Microcephaly 18, Primary, Autosomal Dominant and Myopathy, Centronuclear, 2. Gene Ontology (GO) annotations related to this gene include binding and beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase activity. An important paralog of this gene is WDFY4.
GeneHancer (GH) Identifier | GH Type | GH Score |
GH Sources | Gene Association Score | Total Score | TSS distance (kb) | Number of Genes Away | Size (kb) | Transcription Factor Binding Sites |
Gene Targets |
---|---|---|---|---|---|---|---|---|---|---|
GH04J084965 | Promoter/Enhancer | 2 | EPDnew Ensembl ENCODE CraniofacialAtlas | 600.7 | +0.6 | 589 | 3.8 | GATAD2A PRDM10 ZNF629 SOX13 IKZF1 NFKBIZ ETV6 PRDM1 PHF21A ZIC2 | WDFY3-AS2 WDFY3 ARHGAP24 CDS1 | |
GH04J084926 | Promoter | 0.3 | EPDnew | 600.3 | +40.4 | 40369 | 0.1 | WDFY3 RNU6-469P WDFY3-AS2 RF00026-802 CDS1 | ||
GH04J084937 | Enhancer | 0.6 | Ensembl ENCODE | 12.1 | +28.4 | 28390 | 3.8 | JUND BHLHE40 JUN SMARCA4 HNF4A POLR2A | WDFY3-AS2 WDFY3 WDFY3-AS1 RF00026-802 RNU6-469P CDS1 | |
GH04J084945 | Enhancer | 0.6 | Ensembl ENCODE | 11.2 | +21.5 | 21490 | 3.6 | CEBPA CEBPB NR2F6 HLF | WDFY3-AS2 WDFY3 RNU6-469P WDFY3-AS1 RF00026-802 CDS1 | |
GH04J084592 | Enhancer | 0.6 | Ensembl | 10.5 | +374.0 | 373989 | 3.4 | ARNT ZNF157 ZSCAN5C FOXA2 OSR2 MYNN ATF2 ZFHX2 ZNF530 ZNF843 | WDFY3 WDFY3-AS2 FJ601684-348 CDS1 lnc-NKX6-1-5 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0003831 | beta-N-acetylglucosaminylglycopeptide beta-1,4-galactosyltransferase activity | IEA | -- |
GO:0005515 | protein binding | IPI | 18083104 |
GO:0005545 | 1-phosphatidylinositol binding | IDA | 15292400 |
GO:0008289 | lipid binding | IEA | -- |
GO:0046872 | metal ion binding | IEA | -- |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | IEA | -- |
GO:0005635 | nuclear envelope | IDA | 15292400 |
GO:0005654 | nucleoplasm | IDA | -- |
GO:0005730 | nucleolus | IDA | -- |
GO:0005737 | cytoplasm | IEA,IDA | 15292400 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006914 | autophagy | IEA | -- |
GO:0007275 | multicellular organism development | IEA | -- |
GO:0035973 | aggrephagy | IMP | 20168092 |
This gene was present in the common ancestor of eukaryotes.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | WDFY3 30 31 |
|
OneToOne | |
Oppossum (Monodelphis domestica) |
Mammalia | WDFY3 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | WDFY3 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | WDFY3 30 31 |
|
OneToOne | |
Platypus (Ornithorhynchus anatinus) |
Mammalia | WDFY3 31 |
|
OneToOne | |
Mouse (Mus musculus) |
Mammalia | Wdfy3 30 17 31 |
|
OneToOne | |
Rat (Rattus norvegicus) |
Mammalia | Wdfy3 30 |
|
||
Chicken (Gallus gallus) |
Aves | WDFY3 30 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | WDFY3 31 |
|
OneToOne | |
Tropical Clawed Frog (Silurana tropicalis) |
Amphibia | wdfy3 30 |
|
||
Str.18129 30 |
|
||||
Zebrafish (Danio rerio) |
Actinopterygii | wdfy3 30 31 |
|
OneToOne | |
Dr.17425 30 |
|
||||
Fruit Fly (Drosophila melanogaster) |
Insecta | bchs 30 31 |
|
OneToOne | |
Worm (Caenorhabditis elegans) |
Secernentea | C26H9A.2 30 31 |
|
OneToOne | |
Baker's yeast (Saccharomyces cerevisiae) |
Saccharomycetes | BPH1 33 |
|
|
|
Rice (Oryza sativa) |
Liliopsida | Os.23284 30 |
|
SNP ID | Clinical significance and condition | Chr 04 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
735129 | Likely Benign: not provided | 84,684,123(-) | C/T | SYNONYMOUS_VARIANT | |
742591 | Likely Benign: not provided | 84,817,423(-) | G/A | MISSENSE_VARIANT | |
745292 | Benign: not provided | 84,737,251(-) | G/A | SYNONYMOUS_VARIANT | |
770154 | Benign: not provided | 84,841,185(-) | G/A | MISSENSE_VARIANT | |
778311 | Benign: not provided | 84,783,083(-) | T/C | INTRON_VARIANT |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
esv1008012 | CNV | insertion | 20482838 |
esv3326890 | CNV | insertion | 20981092 |
esv3601226 | CNV | loss | 21293372 |
esv3601227 | CNV | loss | 21293372 |
esv3601228 | CNV | loss | 21293372 |
nsv1139277 | CNV | deletion | 24896259 |
nsv508295 | CNV | deletion | 20534489 |
nsv519588 | CNV | gain | 19592680 |
nsv527581 | CNV | loss | 19592680 |
Disorder | Aliases | PubMed IDs |
---|---|---|
microcephaly 18, primary, autosomal dominant |
|
|
myopathy, centronuclear, 2 |
|
|
microcephaly 19, primary, autosomal recessive |
|
|
microcephaly |
|
|
chediak-higashi syndrome |
|
|