Incidental Mutation 'IGL02020:Wwp2'
ID183923
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Wwp2
Ensembl Gene ENSMUSG00000031930
Gene NameWW domain containing E3 ubiquitin protein ligase 2
SynonymsAIP2, 1300010O06Rik
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.512) question?
Stock #IGL02020
Quality Score
Status
Chromosome8
Chromosomal Location107436365-107558595 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to A at 107556495 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Glutamine at position 354 (R354Q)
Ref Sequence ENSEMBL: ENSMUSP00000148813 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000166615] [ENSMUST00000212205] [ENSMUST00000212543]
Predicted Effect probably damaging
Transcript: ENSMUST00000166615
AA Change: R793Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000132224
Gene: ENSMUSG00000031930
AA Change: R793Q

DomainStartEndE-ValueType
C2 19 115 1.52e-6 SMART
low complexity region 188 208 N/A INTRINSIC
low complexity region 237 249 N/A INTRINSIC
WW 301 330 4.61e-8 SMART
WW 331 363 4.33e-13 SMART
WW 406 437 2.86e-13 SMART
WW 445 477 3.6e-10 SMART
HECTc 534 870 3.24e-201 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000212205
AA Change: R747Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000212543
AA Change: R354Q

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212559
Predicted Effect noncoding transcript
Transcript: ENSMUST00000212993
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 member of the Nedd4 family of E3 ligases, which play an important role in protein ubiquitination. The encoded protein contains four WW domains and may play a role in multiple processes including chondrogenesis and the regulation of oncogenic signaling pathways via interactions with Smad proteins and the tumor suppressor PTEN. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 10. [provided by RefSeq, Jul 2012]
PHENOTYPE: Mice homozygous for a gene trapped allele exhibit decreased body size, domed skull, short snout, twisted snout and overgrown mandibular incisors. Mice homozygous for a different knock-out allele exhibit increased sensitivity to pIpC-treatment. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 29 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrl1 A T 8: 83,932,948 Q711L probably benign Het
Atg9b A C 5: 24,391,058 N205K possibly damaging Het
Brinp3 T C 1: 146,902,127 probably benign Het
Cdh7 A G 1: 110,138,348 Y784C probably damaging Het
Csmd2 T A 4: 128,559,879 D142E probably damaging Het
Dscam A G 16: 96,716,069 L880P probably damaging Het
Gm12355 C A 11: 98,625,509 V13L probably damaging Het
Gm14496 A G 2: 181,996,089 T319A possibly damaging Het
Hr A G 14: 70,556,437 T46A probably benign Het
Ighv1-7 A G 12: 114,538,725 C41R probably damaging Het
Itga3 C T 11: 95,057,390 V539I probably benign Het
Kif13a T A 13: 46,794,019 I830F probably benign Het
Mphosph9 T C 5: 124,258,950 N1110S probably damaging Het
Olfr1029 A G 2: 85,975,235 probably benign Het
Pdia3 G A 2: 121,436,419 probably null Het
Phpt1 T C 2: 25,574,209 I87M probably damaging Het
Psd3 T C 8: 67,974,170 probably benign Het
Ranbp2 A G 10: 58,479,947 E2163G probably damaging Het
Ranbp6 T C 19: 29,809,776 I1059V probably benign Het
Runx2 C T 17: 44,658,599 G253D probably damaging Het
S100a5 A G 3: 90,609,814 probably benign Het
Skint1 T A 4: 112,025,527 M256K probably benign Het
Slc9a3 C T 13: 74,158,848 A364V probably damaging Het
Trip11 C T 12: 101,884,313 R879Q probably damaging Het
Tubgcp3 T C 8: 12,637,780 T588A possibly damaging Het
Vmn2r100 T A 17: 19,504,938 V43E possibly damaging Het
Washc4 T C 10: 83,564,472 S421P probably damaging Het
Wdr38 A T 2: 38,998,412 N7I probably damaging Het
Zfp804b T A 5: 6,769,118 Q1315L probably damaging Het
Other mutations in Wwp2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01383:Wwp2 APN 8 107533291 critical splice donor site probably null
IGL01411:Wwp2 APN 8 107506345 missense probably benign 0.07
IGL01503:Wwp2 APN 8 107549781 missense probably damaging 0.97
IGL01543:Wwp2 APN 8 107483368 missense probably damaging 1.00
IGL01998:Wwp2 APN 8 107549521 missense probably damaging 1.00
IGL02089:Wwp2 APN 8 107554057 missense probably damaging 1.00
IGL02131:Wwp2 APN 8 107552318 missense probably damaging 0.99
IGL02352:Wwp2 APN 8 107540646 nonsense probably null
IGL02359:Wwp2 APN 8 107540646 nonsense probably null
IGL02419:Wwp2 APN 8 107549815 missense probably damaging 1.00
IGL02528:Wwp2 APN 8 107554467 missense probably benign 0.06
R0639:Wwp2 UTSW 8 107517946 missense probably benign 0.01
R0834:Wwp2 UTSW 8 107556796 splice site probably benign
R1573:Wwp2 UTSW 8 107548489 missense probably damaging 1.00
R1653:Wwp2 UTSW 8 107483410 missense possibly damaging 0.49
R1782:Wwp2 UTSW 8 107506399 frame shift probably null
R1941:Wwp2 UTSW 8 107517915 missense probably benign
R2483:Wwp2 UTSW 8 107548535 missense probably damaging 1.00
R4014:Wwp2 UTSW 8 107485621 missense probably benign 0.03
R4118:Wwp2 UTSW 8 107545459 missense probably benign 0.00
R4402:Wwp2 UTSW 8 107457978 missense probably benign 0.08
R5042:Wwp2 UTSW 8 107548485 missense possibly damaging 0.95
R5117:Wwp2 UTSW 8 107554062 missense possibly damaging 0.86
R5413:Wwp2 UTSW 8 107555078 missense probably damaging 1.00
R6175:Wwp2 UTSW 8 107483407 missense possibly damaging 0.95
R6232:Wwp2 UTSW 8 107506345 missense probably benign 0.03
R6323:Wwp2 UTSW 8 107540671 missense probably damaging 1.00
R6759:Wwp2 UTSW 8 107540682 missense probably damaging 1.00
R6941:Wwp2 UTSW 8 107548502 missense probably damaging 1.00
R7043:Wwp2 UTSW 8 107457900 missense probably benign 0.00
R7109:Wwp2 UTSW 8 107483356 missense probably benign 0.28
R7457:Wwp2 UTSW 8 107517960 missense probably benign 0.05
R8027:Wwp2 UTSW 8 107555477 missense probably damaging 1.00
X0066:Wwp2 UTSW 8 107518023 missense probably benign
Z1088:Wwp2 UTSW 8 107555087 missense probably damaging 1.00
Posted On2014-05-07