Incidental Mutation 'IGL02884:Wee1'
ID 362936
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Wee1
Ensembl Gene ENSMUSG00000031016
Gene Name WEE 1 homolog 1 (S. pombe)
Synonyms Wee1A
Accession Numbers
Essential gene? Essential (E-score: 1.000) question?
Stock # IGL02884
Quality Score
Status
Chromosome 7
Chromosomal Location 109721266-109742506 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 109725269 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Isoleucine to Valine at position 304 (I304V)
Ref Sequence ENSEMBL: ENSMUSP00000033326 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000033326]
AlphaFold P47810
Predicted Effect probably benign
Transcript: ENSMUST00000033326
AA Change: I304V

PolyPhen 2 Score 0.016 (Sensitivity: 0.95; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000033326
Gene: ENSMUSG00000031016
AA Change: I304V

DomainStartEndE-ValueType
low complexity region 62 112 N/A INTRINSIC
Pfam:Pkinase_Tyr 298 566 1.9e-26 PFAM
Pfam:Pkinase 298 568 1.7e-61 PFAM
low complexity region 620 631 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185931
Predicted Effect noncoding transcript
Transcript: ENSMUST00000210940
Coding Region Coverage
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a nuclear protein, which is a tyrosine kinase belonging to the Ser/Thr family of protein kinases. This protein catalyzes the inhibitory tyrosine phosphorylation of CDC2/cyclin B kinase, and appears to coordinate the transition between DNA replication and mitosis by protecting the nucleus from cytoplasmically activated CDC2 kinase. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a transgenic gene disruption may exhibit embryonic lethality at E7. Mice homozygous for a knock-out allele exhibit lethality between E3.5 and E7.5 with reduced proliferation, increased apoptosis and abnormal G2/M checkpoint function. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930438A08Rik A G 11: 58,178,302 (GRCm39) I121V probably benign Het
Adprh C T 16: 38,266,396 (GRCm39) V249I probably benign Het
Akap11 A T 14: 78,736,402 (GRCm39) M1797K probably benign Het
Akap6 T A 12: 52,933,405 (GRCm39) I299N probably benign Het
Akr1c12 A T 13: 4,322,211 (GRCm39) M277K possibly damaging Het
Ankrd17 A T 5: 90,412,616 (GRCm39) M1236K probably damaging Het
Arhgef11 A G 3: 87,635,313 (GRCm39) D874G probably damaging Het
Atg4b T C 1: 93,715,437 (GRCm39) probably benign Het
Bcl9 G A 3: 97,117,368 (GRCm39) P442L probably damaging Het
Ccdc107 A T 4: 43,495,228 (GRCm39) K98* probably null Het
Cenpl A G 1: 160,913,619 (GRCm39) Q343R probably benign Het
Cep104 T C 4: 154,074,319 (GRCm39) C524R probably damaging Het
Clec3b C T 9: 122,985,827 (GRCm39) T75I probably benign Het
Col13a1 A T 10: 61,741,064 (GRCm39) probably benign Het
Crot C T 5: 9,028,197 (GRCm39) probably null Het
Ddo G A 10: 40,513,360 (GRCm39) V101I probably benign Het
Disp2 T C 2: 118,618,032 (GRCm39) probably benign Het
Dnmt3b A C 2: 153,516,297 (GRCm39) Y474S probably damaging Het
Dpp6 T A 5: 27,839,554 (GRCm39) N298K possibly damaging Het
Fbf1 C T 11: 116,037,339 (GRCm39) E940K probably damaging Het
Fgd6 A G 10: 93,881,501 (GRCm39) probably benign Het
H2-M10.2 T C 17: 36,595,568 (GRCm39) R241G probably damaging Het
Haghl A T 17: 26,002,072 (GRCm39) F207Y possibly damaging Het
Helt G A 8: 46,745,620 (GRCm39) R88C probably damaging Het
Igf2bp2 T C 16: 21,981,635 (GRCm39) K27E probably benign Het
Il1b T C 2: 129,207,022 (GRCm39) H246R probably benign Het
Itprid1 T C 6: 55,851,339 (GRCm39) probably null Het
Kcnu1 C T 8: 26,411,556 (GRCm39) S167L probably damaging Het
Kif16b A T 2: 142,544,534 (GRCm39) probably benign Het
Myh7 A T 14: 55,230,276 (GRCm39) S19T probably benign Het
Ncaph2 T C 15: 89,248,447 (GRCm39) probably null Het
Nlrp4c T C 7: 6,101,951 (GRCm39) L879P probably damaging Het
Nqo2 T A 13: 34,156,344 (GRCm39) N19K probably damaging Het
Or2r2 C T 6: 42,463,540 (GRCm39) V196M probably damaging Het
Osbpl1a C A 18: 12,952,635 (GRCm39) G93* probably null Het
Pdxdc1 A G 16: 13,661,659 (GRCm39) F459L possibly damaging Het
Phc2 A T 4: 128,601,809 (GRCm39) H88L probably damaging Het
Pkd1l2 G A 8: 117,792,484 (GRCm39) T436I probably benign Het
Ptchd4 A T 17: 42,813,340 (GRCm39) T414S possibly damaging Het
Rab7b A G 1: 131,626,280 (GRCm39) R103G probably damaging Het
Retnla A G 16: 48,662,943 (GRCm39) Y3C probably benign Het
Samd7 G A 3: 30,810,322 (GRCm39) R113H probably damaging Het
Shisa9 G A 16: 11,814,907 (GRCm39) probably benign Het
Soat1 A T 1: 156,268,926 (GRCm39) I208N possibly damaging Het
Stab1 C A 14: 30,872,100 (GRCm39) probably null Het
Tti2 C T 8: 31,641,505 (GRCm39) L210F possibly damaging Het
Ube2v2 A G 16: 15,374,349 (GRCm39) V77A probably benign Het
Ubr5 T C 15: 37,998,620 (GRCm39) E1617G probably damaging Het
Vmn2r16 T A 5: 109,508,757 (GRCm39) I495K possibly damaging Het
Vwce G T 19: 10,623,943 (GRCm39) R278L possibly damaging Het
Wdr26 C T 1: 181,010,349 (GRCm39) A551T probably damaging Het
Xrcc5 C T 1: 72,385,396 (GRCm39) H496Y possibly damaging Het
Zfp142 G T 1: 74,611,142 (GRCm39) S884R probably damaging Het
Other mutations in Wee1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00693:Wee1 APN 7 109,734,060 (GRCm39) splice site probably null
IGL00981:Wee1 APN 7 109,738,876 (GRCm39) missense probably damaging 1.00
IGL01017:Wee1 APN 7 109,725,055 (GRCm39) missense possibly damaging 0.93
IGL01357:Wee1 APN 7 109,741,242 (GRCm39) missense probably benign 0.39
IGL01838:Wee1 APN 7 109,723,744 (GRCm39) missense probably benign 0.01
IGL01970:Wee1 APN 7 109,738,457 (GRCm39) missense probably damaging 1.00
IGL02396:Wee1 APN 7 109,741,300 (GRCm39) missense probably damaging 1.00
IGL02511:Wee1 APN 7 109,738,483 (GRCm39) missense possibly damaging 0.55
IGL03085:Wee1 APN 7 109,723,805 (GRCm39) missense probably damaging 1.00
IGL03221:Wee1 APN 7 109,726,024 (GRCm39) missense probably damaging 1.00
IGL03383:Wee1 APN 7 109,738,899 (GRCm39) missense probably damaging 1.00
R0220:Wee1 UTSW 7 109,723,733 (GRCm39) missense probably benign 0.10
R1934:Wee1 UTSW 7 109,721,698 (GRCm39) missense probably benign 0.06
R3110:Wee1 UTSW 7 109,730,043 (GRCm39) missense probably damaging 1.00
R3112:Wee1 UTSW 7 109,730,043 (GRCm39) missense probably damaging 1.00
R3978:Wee1 UTSW 7 109,723,762 (GRCm39) missense probably damaging 1.00
R4348:Wee1 UTSW 7 109,730,165 (GRCm39) missense probably damaging 1.00
R5434:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5435:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5436:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5449:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5566:Wee1 UTSW 7 109,725,257 (GRCm39) nonsense probably null
R5630:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5632:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5685:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5694:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5807:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R5941:Wee1 UTSW 7 109,723,776 (GRCm39) frame shift probably null
R6044:Wee1 UTSW 7 109,738,513 (GRCm39) missense probably benign 0.00
R6163:Wee1 UTSW 7 109,734,858 (GRCm39) missense probably damaging 1.00
R6826:Wee1 UTSW 7 109,723,870 (GRCm39) critical splice donor site probably null
R7203:Wee1 UTSW 7 109,734,001 (GRCm39) missense probably benign 0.00
R7835:Wee1 UTSW 7 109,730,085 (GRCm39) nonsense probably null
R8273:Wee1 UTSW 7 109,723,691 (GRCm39) missense probably benign 0.00
R8953:Wee1 UTSW 7 109,723,691 (GRCm39) missense probably benign 0.00
R9077:Wee1 UTSW 7 109,725,963 (GRCm39) missense probably damaging 1.00
R9336:Wee1 UTSW 7 109,721,689 (GRCm39) missense probably damaging 1.00
R9463:Wee1 UTSW 7 109,721,917 (GRCm39) missense probably damaging 1.00
R9673:Wee1 UTSW 7 109,725,210 (GRCm39) missense probably damaging 0.98
R9748:Wee1 UTSW 7 109,721,722 (GRCm39) nonsense probably null
Posted On 2015-12-18