Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
126248
Gene name Gene Name - the full gene name approved by the HGNC.
WD repeat domain 88
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
WDR88
Synonyms (NCBI Gene) Gene synonyms aliases
PQWD
Chromosome Chromosome number
19
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.11
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1491897 hsa-miR-3136-3p CLIP-seq
MIRT1491898 hsa-miR-3184 CLIP-seq
MIRT1491899 hsa-miR-3192 CLIP-seq
MIRT1491900 hsa-miR-3660 CLIP-seq
MIRT1491901 hsa-miR-3689a-3p CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32814053
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein
UniProt ID Q6ZMY6
Protein name WD repeat-containing protein 88 (PQQ repeat and WD repeat-containing protein)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00400 WD40 93 130 WD domain, G-beta repeat Repeat
PF01011 PQQ 159 191 PQQ enzyme repeat Repeat
PF00400 WD40 219 258 WD domain, G-beta repeat Repeat
PF00400 WD40 263 301 WD domain, G-beta repeat Repeat
PF00400 WD40 311 349 WD domain, G-beta repeat Repeat
PF00400 WD40 354 391 WD domain, G-beta repeat Repeat
Sequence
MASPPRCSPTAHDRECKLPPPSAPASEYCPGKLSWGTMARALGRFKLSIPHTHLLATLDP
LALDREPPPHLLPEKHQVPEKLIWGDQDPLSKIPFKILSGHEHAVSTCHFCVDDTKLLSG
SYDCTVKLWD
PVDGSVVRDFEHRPKAPVVECSITGDSSRVIAASYDKTVRAWDLETGKLL
WKVRYDTFIVS
CKFSPDGKYVVSGFDVDHGICIMDAENITTVSVIKDHHTRSITSCCFDP
DSQRVASVSLDRCIKIWD
VTSQATLLTITKAHSNAISNCCFTFSGHFLCTSSWDKNLKIW
N
VHTGEFRNCGACVTLMQGHEGSVSSCHFARDSSFLISGGFDRTVAIWDVAEGYRKLSLK
GHNDWVMDVAISNNKKWILSASKDRTMRLWN
IEEIDEIPLVIKYKKAVGLKLKQCERCDR
PFSIFKSDTSSEMFTQCVFCRIDTRGLPADTSSSSSSSERENSPPPRGSKDD
Sequence length 472
Interactions View interactions
<
Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Alzheimer disease Alzheimer's disease or family history of Alzheimer's disease N/A N/A GWAS
Prostate cancer Prostate cancer N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Candidiasis Associate 36167494