Incidental Mutation 'IGL01503:Wwp2'
| ID |
88937 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Wwp2
|
| Ensembl Gene |
ENSMUSG00000031930 |
| Gene Name |
WW domain containing E3 ubiquitin protein ligase 2 |
| Synonyms |
AIP2, 1300010O06Rik |
| Accession Numbers |
|
| Essential gene? |
Possibly non essential
(E-score: 0.393)
|
| Stock # |
IGL01503
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
8 |
| Chromosomal Location |
108162997-108285227 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 108276413 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Serine to Proline
at position 508
(S508P)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000132224
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000166615]
[ENSMUST00000212205]
[ENSMUST00000212543]
|
| AlphaFold |
Q9DBH0 |
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000083505
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000166615
AA Change: S508P
PolyPhen 2
Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000132224
Gene: ENSMUSG00000031930
AA Change: S508P
| Domain | Start | End | E-Value | Type |
|---|
|
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 |
noncoding transcript
Transcript: ENSMUST00000212063
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000212205
AA Change: S462P
PolyPhen 2
Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000212543
AA Change: S69P
PolyPhen 2
Score 0.851 (Sensitivity: 0.83; Specificity: 0.93)
|
| 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: 39 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110057P08Rik |
T |
A |
16: 88,971,757 (GRCm39) |
Y26* |
probably null |
Het |
| Aadacl4fm4 |
T |
A |
4: 144,401,137 (GRCm39) |
I116F |
probably damaging |
Het |
| Arpc1a |
T |
C |
5: 145,032,964 (GRCm39) |
V91A |
probably damaging |
Het |
| Atp2a1 |
T |
A |
7: 126,047,750 (GRCm39) |
I687F |
probably damaging |
Het |
| B3gnt5 |
A |
C |
16: 19,588,531 (GRCm39) |
Y250S |
probably damaging |
Het |
| Brip1 |
A |
G |
11: 85,952,703 (GRCm39) |
V1026A |
probably benign |
Het |
| C1s2 |
T |
C |
6: 124,602,612 (GRCm39) |
D527G |
probably damaging |
Het |
| Chrna5 |
T |
A |
9: 54,905,455 (GRCm39) |
|
probably benign |
Het |
| Cltc |
C |
A |
11: 86,586,526 (GRCm39) |
|
probably benign |
Het |
| Dgkh |
T |
G |
14: 78,853,710 (GRCm39) |
I439L |
possibly damaging |
Het |
| Dnajc16 |
G |
A |
4: 141,491,008 (GRCm39) |
T714I |
possibly damaging |
Het |
| Fam13a |
A |
T |
6: 58,933,065 (GRCm39) |
I349N |
probably damaging |
Het |
| Fig4 |
C |
T |
10: 41,132,514 (GRCm39) |
D431N |
probably benign |
Het |
| Gabra4 |
A |
T |
5: 71,798,429 (GRCm39) |
N183K |
possibly damaging |
Het |
| Ggt5 |
C |
T |
10: 75,445,944 (GRCm39) |
|
probably benign |
Het |
| Hdac6 |
A |
G |
X: 7,798,418 (GRCm39) |
L798P |
probably damaging |
Het |
| Hectd4 |
T |
C |
5: 121,456,714 (GRCm39) |
V2030A |
probably benign |
Het |
| Hecw2 |
A |
G |
1: 53,866,120 (GRCm39) |
Y1514H |
probably damaging |
Het |
| Hmcn1 |
T |
C |
1: 150,480,823 (GRCm39) |
D4451G |
probably benign |
Het |
| Krtcap3 |
T |
C |
5: 31,409,167 (GRCm39) |
|
probably benign |
Het |
| Ltn1 |
A |
T |
16: 87,217,695 (GRCm39) |
|
probably benign |
Het |
| Mapkapk2 |
T |
C |
1: 130,986,499 (GRCm39) |
M1V |
probably null |
Het |
| Mical3 |
A |
T |
6: 120,935,537 (GRCm39) |
I1663N |
probably benign |
Het |
| Mvp |
G |
T |
7: 126,601,133 (GRCm39) |
|
probably benign |
Het |
| Myo5c |
A |
G |
9: 75,170,324 (GRCm39) |
I485V |
probably damaging |
Het |
| N4bp2 |
T |
A |
5: 65,960,890 (GRCm39) |
C520* |
probably null |
Het |
| Nos2 |
A |
G |
11: 78,836,689 (GRCm39) |
|
probably benign |
Het |
| Ogdh |
G |
A |
11: 6,305,069 (GRCm39) |
V925M |
probably damaging |
Het |
| Pde2a |
T |
A |
7: 101,151,143 (GRCm39) |
|
probably benign |
Het |
| Plpp6 |
A |
G |
19: 28,942,279 (GRCm39) |
*293W |
probably null |
Het |
| Pole |
T |
A |
5: 110,451,750 (GRCm39) |
I864K |
probably damaging |
Het |
| Rexo4 |
A |
T |
2: 26,850,645 (GRCm39) |
I239N |
probably benign |
Het |
| Scn1a |
T |
A |
2: 66,152,687 (GRCm39) |
I748F |
probably damaging |
Het |
| Sfmbt2 |
A |
T |
2: 10,584,165 (GRCm39) |
R841* |
probably null |
Het |
| Sh3bp5l |
A |
G |
11: 58,228,827 (GRCm39) |
N100S |
probably damaging |
Het |
| Spic |
T |
A |
10: 88,511,623 (GRCm39) |
D211V |
probably damaging |
Het |
| Stab2 |
A |
G |
10: 86,776,477 (GRCm39) |
|
probably benign |
Het |
| Tshr |
A |
G |
12: 91,478,708 (GRCm39) |
Y83C |
probably damaging |
Het |
| Vsir |
A |
G |
10: 60,204,373 (GRCm39) |
E172G |
probably damaging |
Het |
|
| Other mutations in Wwp2 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01383:Wwp2
|
APN |
8 |
108,259,923 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL01411:Wwp2
|
APN |
8 |
108,232,977 (GRCm39) |
missense |
probably benign |
0.07 |
|
IGL01543:Wwp2
|
APN |
8 |
108,210,000 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01998:Wwp2
|
APN |
8 |
108,276,153 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02020:Wwp2
|
APN |
8 |
108,283,127 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02089:Wwp2
|
APN |
8 |
108,280,689 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02131:Wwp2
|
APN |
8 |
108,278,950 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02352:Wwp2
|
APN |
8 |
108,267,278 (GRCm39) |
nonsense |
probably null |
|
|
IGL02359:Wwp2
|
APN |
8 |
108,267,278 (GRCm39) |
nonsense |
probably null |
|
|
IGL02419:Wwp2
|
APN |
8 |
108,276,447 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02528:Wwp2
|
APN |
8 |
108,281,099 (GRCm39) |
missense |
probably benign |
0.06 |
|
R0639:Wwp2
|
UTSW |
8 |
108,244,578 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0834:Wwp2
|
UTSW |
8 |
108,283,428 (GRCm39) |
splice site |
probably benign |
|
|
R1573:Wwp2
|
UTSW |
8 |
108,275,121 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1653:Wwp2
|
UTSW |
8 |
108,210,042 (GRCm39) |
missense |
possibly damaging |
0.49 |
|
R1782:Wwp2
|
UTSW |
8 |
108,233,031 (GRCm39) |
frame shift |
probably null |
|
|
R1941:Wwp2
|
UTSW |
8 |
108,244,547 (GRCm39) |
missense |
probably benign |
|
|
R2483:Wwp2
|
UTSW |
8 |
108,275,167 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4014:Wwp2
|
UTSW |
8 |
108,212,253 (GRCm39) |
missense |
probably benign |
0.03 |
|
R4118:Wwp2
|
UTSW |
8 |
108,272,091 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4402:Wwp2
|
UTSW |
8 |
108,184,610 (GRCm39) |
missense |
probably benign |
0.08 |
|
R5042:Wwp2
|
UTSW |
8 |
108,275,117 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5117:Wwp2
|
UTSW |
8 |
108,280,694 (GRCm39) |
missense |
possibly damaging |
0.86 |
|
R5413:Wwp2
|
UTSW |
8 |
108,281,710 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6175:Wwp2
|
UTSW |
8 |
108,210,039 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R6232:Wwp2
|
UTSW |
8 |
108,232,977 (GRCm39) |
missense |
probably benign |
0.03 |
|
R6323:Wwp2
|
UTSW |
8 |
108,267,303 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6759:Wwp2
|
UTSW |
8 |
108,267,314 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6941:Wwp2
|
UTSW |
8 |
108,275,134 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7043:Wwp2
|
UTSW |
8 |
108,184,532 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7109:Wwp2
|
UTSW |
8 |
108,209,988 (GRCm39) |
missense |
probably benign |
0.28 |
|
R7457:Wwp2
|
UTSW |
8 |
108,244,592 (GRCm39) |
missense |
probably benign |
0.05 |
|
R8027:Wwp2
|
UTSW |
8 |
108,282,109 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8704:Wwp2
|
UTSW |
8 |
108,212,228 (GRCm39) |
missense |
probably benign |
|
|
R8796:Wwp2
|
UTSW |
8 |
108,283,189 (GRCm39) |
missense |
probably null |
1.00 |
|
R8844:Wwp2
|
UTSW |
8 |
108,210,048 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9627:Wwp2
|
UTSW |
8 |
108,278,959 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0066:Wwp2
|
UTSW |
8 |
108,244,655 (GRCm39) |
missense |
probably benign |
|
|
Z1088:Wwp2
|
UTSW |
8 |
108,281,719 (GRCm39) |
missense |
probably damaging |
1.00 |
|
| Posted On |
2013-12-03 |
Incidental Mutation