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This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. This gene is excluded as a candidate for a form of nonsyndromic deafness (DFNB10), but is still a candidate for other disorders mapped to 21q22.3 as well as for the development of Down syndrome phenotypes. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, May 2012]
WDR4 (WD Repeat Domain 4) is a Protein Coding gene. Diseases associated with WDR4 include Galloway-Mowat Syndrome 6 and Microcephaly, Growth Deficiency, Seizures, And Brain Malformations. Among its related pathways are Gene Expression and tRNA processing. Gene Ontology (GO) annotations related to this gene include tRNA (guanine-N7-)-methyltransferase activity.
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005515 | protein binding | IPI | 15861136 |
GO:0008176 | contributes_to tRNA (guanine-N7-)-methyltransferase activity | IBA,IDA | 12403464 |
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0005634 | nucleus | IBA,IDA | 15861136 |
GO:0005654 | nucleoplasm | HDA,IDA | -- |
GO:0005694 | chromosome | IEA | -- |
GO:0005829 | cytosol | IBA,IDA | -- |
GO:0043527 | tRNA methyltransferase complex | IBA,IDA | 12403464 |
SuperPathway | Contained pathways | ||
---|---|---|---|
1 | tRNA processing |
.55
|
|
2 | Gene Expression |
.48
|
GO ID | Qualified GO term | Evidence | PubMed IDs |
---|---|---|---|
GO:0006400 | tRNA modification | IDA | 15861136 |
GO:0006974 | cellular response to DNA damage stimulus | IEA | -- |
GO:0008033 | tRNA processing | IEA | -- |
GO:0030488 | tRNA methylation | IEA | -- |
GO:0036265 | RNA (guanine-N7)-methylation | IEA | -- |
ExUns: | 1a | · | 1b | ^ | 2 | ^ | 3a | · | 3b | ^ | 4 | ^ | 5a | · | 5b | ^ | 6 | ^ | 7a | · | 7b | ^ | 8 | ^ | 9 | ^ | 10 | ^ | 11 | ^ | 12 | ^ | 13a | · | 13b | ^ | 14 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
SP1: | - | - | - | - | |||||||||||||||||||||||||||||||||
SP2: | - | - | - | - | - | ||||||||||||||||||||||||||||||||
SP3: | - | - | - | ||||||||||||||||||||||||||||||||||
SP4: | - | - | |||||||||||||||||||||||||||||||||||
SP5: | |||||||||||||||||||||||||||||||||||||
SP6: | - |
This gene was present in the common ancestor of animals and fungi.
Organism | Taxonomy | Gene | Similarity | Type | Details |
---|---|---|---|---|---|
Chimpanzee (Pan troglodytes) |
Mammalia | WDR4 30 31 |
|
OneToOne | |
Dog (Canis familiaris) |
Mammalia | WDR4 30 31 |
|
OneToOne | |
Cow (Bos Taurus) |
Mammalia | WDR4 30 31 |
|
OneToOne | |
Mouse (Mus musculus) |
Mammalia | Wdr4 30 17 31 |
|
OneToOne | |
Rat (Rattus norvegicus) |
Mammalia | Wdr4 30 |
|
||
Oppossum (Monodelphis domestica) |
Mammalia | WDR4 31 |
|
OneToOne | |
Platypus (Ornithorhynchus anatinus) |
Mammalia | WDR4 31 |
|
OneToOne | |
Chicken (Gallus gallus) |
Aves | WDR4 30 31 |
|
OneToOne | |
Lizard (Anolis carolinensis) |
Reptilia | WDR4 31 |
|
OneToOne | |
African clawed frog (Xenopus laevis) |
Amphibia | wdr4-prov 30 |
|
||
Tropical Clawed Frog (Silurana tropicalis) |
Amphibia | Str.4956 30 |
|
||
Zebrafish (Danio rerio) |
Actinopterygii | LOC100536637 30 |
|
||
wdr4 31 |
|
OneToMany | |||
FP017279.3 31 |
|
OneToMany | |||
Fruit Fly (Drosophila melanogaster) |
Insecta | wuho 31 |
|
OneToOne | |
Worm (Caenorhabditis elegans) |
Secernentea | Y102E9.2 31 |
|
OneToOne | |
Baker's yeast (Saccharomyces cerevisiae) |
Saccharomycetes | TRM82 31 33 |
|
OneToOne |
SNP ID | Clinical significance and condition | Chr 21 pos | Variation | AA Info | Type |
---|---|---|---|---|---|
710985 | Benign: not provided | 42,852,333(-) | G/A | INTRON_VARIANT | |
726110 | Likely Benign: not provided | 42,852,264(-) | T/C | MISSENSE_VARIANT,NON_CODING_TRANSCRIPT_VARIANT | |
773615 | Benign: not provided | 42,879,463(-) | C/T | SYNONYMOUS_VARIANT,FIVE_PRIME_UTR_VARIANT,INTRON_VARIANT | |
777624 | Benign: not provided | 42,863,593(-) | G/A | NON_CODING_TRANSCRIPT_VARIANT,SYNONYMOUS_VARIANT,FIVE_PRIME_UTR_VARIANT | |
rs1292041526 | Pathogenic: MICROCEPHALY, GROWTH DEFICIENCY, SEIZURES, AND BRAIN MALFORMATIONS. Pathogenic: GALLOWAY-MOWAT SYNDROME 6. Galloway-Mowat syndrome 6 (GAMOS6) [MIM:618347] | 42,862,339(-) | C/AC/Tp.Arg170Gln | MISSENSE_VARIANT,NON_CODING_TRANSCRIPT_VARIANT |
Variant ID | Type | Subtype | PubMed ID |
---|---|---|---|
esv2666871 | CNV | deletion | 23128226 |
esv2723576 | CNV | deletion | 23290073 |
esv2723577 | CNV | deletion | 23290073 |
esv2723578 | CNV | deletion | 23290073 |
esv2723579 | CNV | deletion | 23290073 |
esv3568210 | CNV | loss | 25503493 |
esv3584478 | CNV | gain | 24956385 |
esv3647094 | CNV | loss | 21293372 |
esv3647095 | CNV | loss | 21293372 |
nsv1135908 | CNV | deletion | 24896259 |
nsv587657 | CNV | gain | 21841781 |
nsv587659 | CNV | loss | 21841781 |
nsv834105 | CNV | loss | 17160897 |
Disorder | Aliases | PubMed IDs |
---|---|---|
galloway-mowat syndrome 6 |
|
|
microcephaly, growth deficiency, seizures, and brain malformations |
|
|
galloway-mowat syndrome |
|
|
microcephaly |
|
|
thiamine-responsive megaloblastic anemia syndrome |
|
|