Gene Gene information from NCBI Gene database.
Entrez ID 494551
Gene name WEE2 oocyte meiosis inhibiting kinase
Gene symbol WEE2
Synonyms (NCBI Gene)
OOMD5OZEMA5WEE1B
Chromosome 7
Chromosome location 7q34
miRNA miRNA information provided by mirtarbase database.
49
miRTarBase ID miRNA Experiments Reference
MIRT644260 hsa-miR-3662 HITS-CLIP 23824327
MIRT644259 hsa-miR-590-5p HITS-CLIP 23824327
MIRT644258 hsa-miR-3163 HITS-CLIP 23824327
MIRT644257 hsa-miR-664a-3p HITS-CLIP 23824327
MIRT644256 hsa-miR-6832-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
30
GO ID Ontology Definition Evidence Reference
GO:0000166 Function Nucleotide binding IEA
GO:0000278 Process Mitotic cell cycle IEA
GO:0000287 Function Magnesium ion binding IEA
GO:0004672 Function Protein kinase activity IEA
GO:0004713 Function Protein tyrosine kinase activity IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614084 19684 ENSG00000214102
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P0C1S8
Protein name Wee1-like protein kinase 2 (EC 2.7.10.2) (Wee1-like protein kinase 1B) (Wee1B kinase)
Protein function Oocyte-specific protein tyrosine kinase that phosphorylates and inhibits CDK1/CDC2 and acts as a key regulator of meiosis during both prophase I and metaphase II (PubMed:29606300). Required to maintain meiotic arrest in oocytes during the germin
PDB 5VDK
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00069 Pkinase 212 486 Protein kinase domain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in oocytes (at protein level) (PubMed:29606300). May also be expressed in testis (PubMed:11029659). {ECO:0000269|PubMed:11029659, ECO:0000269|PubMed:29606300}.
Sequence
MDDKDIDKELRQKLNFSYCEETEIEGQKKVEESREASSQTPEKGEVQDSEAKGTPPWTPL
SNVHELDTSSEKDKESPDQILRTPVSHPLKCPETPAQPDSRSKLLPSDSPSTPKTMLSRL
VISPTGKLPSRGPKHLKLTPAPLKDEMTSLALVNINPFTPESYKKLFLQSGGKRKIRGDL
EEAGPEEGKGGLPAKRCVLRETNMASRYEKEFLEVEKIGVGEFGTVYKCIKRLDGCVYAI
KRSMKTFTELSNENSALHEVYAHAVLGHHPHVVRYYSSWAEDDHMIIQNEYCNGGSLQAA
ISENTKSGNHFEEPKLKDILLQISLGLNYIHNSSMVHLDIKPSNIFICHKMQSESSGVIE
EVENEADWFLSANVMYKIGDLGHATSINKPKVEEGDSRFLANEILQEDYRHLPKADIFAL
GLTIAVAAGAESLPTNGAAWHHIRKGNFPDVPQELSESFSSLLKNMIQPDAEQRPSAAAL
ARNTVL
RPSLGKTEELQQQLNLEKFKTATLERELREAQQAQSPQGYTHHGDTGVSGTHTG
SRSTKRLVGGKSARSSSFTSGEREPLH
Sequence length 567
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Cell cycle
Human immunodeficiency virus 1 infection
 
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
14
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Oocyte maturation defect 5 Pathogenic; Likely pathogenic rs1554415096, rs1554416415, rs768323979, rs905047580, rs1380657460, rs754062320 RCV000656452
RCV000656453
RCV000656454
RCV001254889
RCV001254890
RCV001254891
WEE2-related disorder Likely pathogenic rs768323979 RCV004758715
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Arteriosclerosis Obliterans Stimulate 33174040
Carcinoma Hepatocellular Associate 32838835
Glioblastoma Associate 32838835, 36168628
Glioma Associate 36747161, 37305396
Infertility Associate 30826994, 31428887
Infertility Female Associate 29606300, 30826994, 30827524, 31428887
Neoplasms Stimulate 32838835
Neoplasms Associate 36747161
Neoplasms Inhibit 37305396
Renal Insufficiency Associate 29606300, 30826994, 30827523, 30827524, 31428887, 33073652, 33904356, 34476630