Gene Gene information from NCBI Gene database.
Entrez ID 126248
Gene name WD repeat domain 88
Gene symbol WDR88
Synonyms (NCBI Gene)
PQWD
Chromosome 19
Chromosome location 19q13.11
miRNA miRNA information provided by mirtarbase database.
39
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 (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 32814053
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
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 from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
DEMENTIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CANCER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
PROSTATE CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Malignant neoplasm of breast Breast Cancer UNIPROT_DG
★☆☆☆☆
Found in Text Mining only