Incidental Mutation 'IGL01338:Wwp1'
| ID |
74688 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Wwp1
|
| Ensembl Gene |
ENSMUSG00000041058 |
| Gene Name |
WW domain containing E3 ubiquitin protein ligase 1 |
| Synonyms |
Tiul1, SDRP1, 8030445B08Rik, AIP5 |
| Accession Numbers |
|
| Essential gene? |
Non essential
(E-score: 0.000)
|
| Stock # |
IGL01338
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
4 |
| Chromosomal Location |
19608303-19708993 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 19627636 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Threonine
at position 753
(I753T)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000103881
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000035982]
[ENSMUST00000108246]
[ENSMUST00000108250]
|
| AlphaFold |
Q8BZZ3 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000035982
AA Change: I753T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000041627
Gene: ENSMUSG00000041058
AA Change: I753T
| Domain | Start | End | E-Value | Type |
|---|
|
C2
|
19 |
113 |
4.19e-9 |
SMART |
|
low complexity region
|
221 |
232 |
N/A |
INTRINSIC |
|
low complexity region
|
266 |
286 |
N/A |
INTRINSIC |
|
WW
|
346 |
378 |
1.03e-14 |
SMART |
|
WW
|
379 |
410 |
7.43e-12 |
SMART |
|
WW
|
453 |
485 |
1.43e-13 |
SMART |
|
WW
|
493 |
525 |
6.82e-11 |
SMART |
|
HECTc
|
582 |
918 |
4.83e-177 |
SMART |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000108246
AA Change: I753T
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
| SMART Domains |
Protein: ENSMUSP00000103881
Gene: ENSMUSG00000041058
AA Change: I753T
| Domain | Start | End | E-Value | Type |
|---|
|
C2
|
19 |
113 |
4.19e-9 |
SMART |
|
low complexity region
|
221 |
232 |
N/A |
INTRINSIC |
|
low complexity region
|
266 |
286 |
N/A |
INTRINSIC |
|
WW
|
346 |
378 |
1.03e-14 |
SMART |
|
WW
|
379 |
410 |
7.43e-12 |
SMART |
|
WW
|
453 |
485 |
1.43e-13 |
SMART |
|
WW
|
493 |
525 |
6.82e-11 |
SMART |
|
HECTc
|
582 |
918 |
4.83e-177 |
SMART |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108250
|
| SMART Domains |
Protein: ENSMUSP00000103885
Gene: ENSMUSG00000078772
| Domain | Start | End | E-Value | Type |
|---|
|
low complexity region
|
31 |
48 |
N/A |
INTRINSIC |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] WW domain-containing proteins are found in all eukaryotes and play an important role in the regulation of a wide variety of cellular functions such as protein degradation, transcription, and RNA splicing. This gene encodes a protein which contains 4 tandem WW domains and a HECT (homologous to the E6-associated protein carboxyl terminus) domain. The encoded protein belongs to a family of NEDD4-like proteins, which are E3 ubiquitin-ligase molecules and regulate key trafficking decisions, including targeting of proteins to proteosomes or lysosomes. Alternative splicing of this gene generates at least 6 transcript variants; however, the full length nature of these transcripts has not been defined. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased osteoblast differentiation of bone marrow-derived stromal cells. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 48 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110004E09Rik |
T |
C |
16: 90,926,048 (GRCm38) |
N266S |
possibly damaging |
Het |
| Adam23 |
A |
G |
1: 63,551,855 (GRCm38) |
T494A |
possibly damaging |
Het |
| Adamts16 |
C |
T |
13: 70,836,115 (GRCm38) |
C143Y |
probably damaging |
Het |
| Cacna1i |
A |
G |
15: 80,348,380 (GRCm38) |
I195V |
probably damaging |
Het |
| Casp7 |
T |
C |
19: 56,404,464 (GRCm38) |
S17P |
probably benign |
Het |
| Cox6a1 |
C |
A |
5: 115,345,839 (GRCm38) |
|
probably benign |
Het |
| Cpvl |
T |
A |
6: 53,974,655 (GRCm38) |
S48C |
possibly damaging |
Het |
| Cyp2b19 |
G |
T |
7: 26,759,417 (GRCm38) |
M138I |
probably benign |
Het |
| Dennd5a |
T |
C |
7: 109,919,404 (GRCm38) |
Y510C |
possibly damaging |
Het |
| Derl2 |
A |
G |
11: 71,010,355 (GRCm38) |
F229S |
possibly damaging |
Het |
| Dlec1 |
A |
G |
9: 119,120,911 (GRCm38) |
E452G |
probably damaging |
Het |
| Dsc2 |
T |
C |
18: 20,047,157 (GRCm38) |
K180E |
probably benign |
Het |
| Dus1l |
G |
A |
11: 120,793,092 (GRCm38) |
R177C |
possibly damaging |
Het |
| Egfr |
A |
G |
11: 16,863,020 (GRCm38) |
I167V |
probably damaging |
Het |
| Fam219b |
A |
T |
9: 57,538,022 (GRCm38) |
|
probably null |
Het |
| Fn1 |
T |
C |
1: 71,626,210 (GRCm38) |
E916G |
probably damaging |
Het |
| Gm2058 |
C |
T |
7: 39,589,156 (GRCm38) |
|
noncoding transcript |
Het |
| Gpd1 |
T |
A |
15: 99,718,175 (GRCm38) |
V22E |
probably damaging |
Het |
| Hsf2 |
T |
C |
10: 57,501,379 (GRCm38) |
F124L |
probably damaging |
Het |
| I0C0044D17Rik |
A |
G |
4: 98,820,099 (GRCm38) |
|
probably benign |
Het |
| Igfbp3 |
A |
T |
11: 7,208,478 (GRCm38) |
F262I |
possibly damaging |
Het |
| Klhl18 |
A |
G |
9: 110,455,433 (GRCm38) |
Y62H |
probably damaging |
Het |
| Lama2 |
C |
T |
10: 27,188,272 (GRCm38) |
E1238K |
probably benign |
Het |
| Man1b1 |
A |
G |
2: 25,338,227 (GRCm38) |
K170E |
probably benign |
Het |
| Mcrs1 |
A |
T |
15: 99,249,501 (GRCm38) |
I39N |
probably damaging |
Het |
| Mug2 |
T |
C |
6: 122,049,628 (GRCm38) |
|
probably benign |
Het |
| Neu3 |
C |
A |
7: 99,813,422 (GRCm38) |
G365W |
probably damaging |
Het |
| Nipal3 |
A |
C |
4: 135,471,883 (GRCm38) |
|
probably null |
Het |
| Nrxn3 |
A |
G |
12: 89,255,034 (GRCm38) |
I528V |
possibly damaging |
Het |
| Olfr122 |
A |
T |
17: 37,771,839 (GRCm38) |
H71L |
possibly damaging |
Het |
| Osbpl8 |
A |
G |
10: 111,267,747 (GRCm38) |
K204R |
probably damaging |
Het |
| Pax8 |
A |
G |
2: 24,435,919 (GRCm38) |
S318P |
possibly damaging |
Het |
| Pcdh18 |
T |
A |
3: 49,756,141 (GRCm38) |
N242Y |
probably damaging |
Het |
| Pkd1l2 |
T |
A |
8: 117,059,520 (GRCm38) |
K649* |
probably null |
Het |
| Ppm1n |
A |
T |
7: 19,279,254 (GRCm38) |
D257E |
probably benign |
Het |
| Pxdn |
A |
G |
12: 30,002,797 (GRCm38) |
E811G |
probably damaging |
Het |
| Relb |
T |
C |
7: 19,616,373 (GRCm38) |
I218V |
probably benign |
Het |
| Rreb1 |
T |
C |
13: 37,931,034 (GRCm38) |
C790R |
probably damaging |
Het |
| Rtkn2 |
G |
T |
10: 68,025,519 (GRCm38) |
C258F |
possibly damaging |
Het |
| Scn11a |
G |
A |
9: 119,784,161 (GRCm38) |
|
probably benign |
Het |
| Snx8 |
G |
A |
5: 140,358,096 (GRCm38) |
R96C |
probably damaging |
Het |
| Syne2 |
A |
T |
12: 76,060,226 (GRCm38) |
T5649S |
possibly damaging |
Het |
| Tm2d3 |
T |
A |
7: 65,695,222 (GRCm38) |
C82* |
probably null |
Het |
| Tnpo2 |
T |
C |
8: 85,040,526 (GRCm38) |
L55P |
probably damaging |
Het |
| Tsc22d2 |
T |
C |
3: 58,417,415 (GRCm38) |
|
probably benign |
Het |
| Ttll3 |
T |
G |
6: 113,394,729 (GRCm38) |
V19G |
probably damaging |
Het |
| Ube2r2 |
A |
G |
4: 41,174,119 (GRCm38) |
I86V |
probably benign |
Het |
| Vps13d |
G |
A |
4: 145,088,322 (GRCm38) |
T3153I |
probably damaging |
Het |
|
| Other mutations in Wwp1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00156:Wwp1
|
APN |
4 |
19,650,360 (GRCm38) |
missense |
probably benign |
|
|
IGL00945:Wwp1
|
APN |
4 |
19,640,193 (GRCm38) |
critical splice donor site |
probably null |
|
|
IGL01960:Wwp1
|
APN |
4 |
19,662,115 (GRCm38) |
splice site |
probably benign |
|
|
IGL02969:Wwp1
|
APN |
4 |
19,623,200 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL03137:Wwp1
|
APN |
4 |
19,678,408 (GRCm38) |
missense |
probably damaging |
0.97 |
|
BB008:Wwp1
|
UTSW |
4 |
19,650,114 (GRCm38) |
critical splice donor site |
probably null |
|
|
BB018:Wwp1
|
UTSW |
4 |
19,650,114 (GRCm38) |
critical splice donor site |
probably null |
|
|
PIT4243001:Wwp1
|
UTSW |
4 |
19,638,631 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R0035:Wwp1
|
UTSW |
4 |
19,631,116 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0109:Wwp1
|
UTSW |
4 |
19,641,725 (GRCm38) |
intron |
probably benign |
|
|
R0240:Wwp1
|
UTSW |
4 |
19,641,734 (GRCm38) |
splice site |
probably null |
|
|
R0240:Wwp1
|
UTSW |
4 |
19,641,734 (GRCm38) |
splice site |
probably null |
|
|
R0391:Wwp1
|
UTSW |
4 |
19,627,911 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0464:Wwp1
|
UTSW |
4 |
19,638,763 (GRCm38) |
intron |
probably benign |
|
|
R1604:Wwp1
|
UTSW |
4 |
19,659,709 (GRCm38) |
missense |
probably benign |
|
|
R1716:Wwp1
|
UTSW |
4 |
19,659,698 (GRCm38) |
missense |
probably benign |
0.00 |
|
R1778:Wwp1
|
UTSW |
4 |
19,627,892 (GRCm38) |
nonsense |
probably null |
|
|
R1832:Wwp1
|
UTSW |
4 |
19,650,197 (GRCm38) |
missense |
probably benign |
0.33 |
|
R2073:Wwp1
|
UTSW |
4 |
19,662,181 (GRCm38) |
missense |
possibly damaging |
0.89 |
|
R2094:Wwp1
|
UTSW |
4 |
19,650,390 (GRCm38) |
missense |
probably benign |
0.00 |
|
R2228:Wwp1
|
UTSW |
4 |
19,641,745 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2229:Wwp1
|
UTSW |
4 |
19,641,745 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2267:Wwp1
|
UTSW |
4 |
19,638,618 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R2334:Wwp1
|
UTSW |
4 |
19,662,032 (GRCm38) |
missense |
probably benign |
0.07 |
|
R2349:Wwp1
|
UTSW |
4 |
19,638,644 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R3761:Wwp1
|
UTSW |
4 |
19,631,085 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4062:Wwp1
|
UTSW |
4 |
19,638,644 (GRCm38) |
missense |
possibly damaging |
0.72 |
|
R4731:Wwp1
|
UTSW |
4 |
19,661,990 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4732:Wwp1
|
UTSW |
4 |
19,661,990 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4733:Wwp1
|
UTSW |
4 |
19,661,990 (GRCm38) |
missense |
probably benign |
0.00 |
|
R4838:Wwp1
|
UTSW |
4 |
19,662,143 (GRCm38) |
missense |
probably benign |
0.31 |
|
R4936:Wwp1
|
UTSW |
4 |
19,638,804 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R5262:Wwp1
|
UTSW |
4 |
19,631,057 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5340:Wwp1
|
UTSW |
4 |
19,638,773 (GRCm38) |
critical splice donor site |
probably null |
|
|
R5847:Wwp1
|
UTSW |
4 |
19,662,174 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R6492:Wwp1
|
UTSW |
4 |
19,650,299 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R6602:Wwp1
|
UTSW |
4 |
19,641,816 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R6628:Wwp1
|
UTSW |
4 |
19,661,963 (GRCm38) |
splice site |
probably null |
|
|
R7017:Wwp1
|
UTSW |
4 |
19,623,124 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7195:Wwp1
|
UTSW |
4 |
19,627,908 (GRCm38) |
missense |
possibly damaging |
0.84 |
|
R7276:Wwp1
|
UTSW |
4 |
19,611,782 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7450:Wwp1
|
UTSW |
4 |
19,640,016 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7488:Wwp1
|
UTSW |
4 |
19,627,660 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7617:Wwp1
|
UTSW |
4 |
19,662,188 (GRCm38) |
missense |
probably benign |
0.00 |
|
R7707:Wwp1
|
UTSW |
4 |
19,627,645 (GRCm38) |
missense |
probably benign |
0.31 |
|
R7812:Wwp1
|
UTSW |
4 |
19,639,991 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7864:Wwp1
|
UTSW |
4 |
19,635,328 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7931:Wwp1
|
UTSW |
4 |
19,650,114 (GRCm38) |
critical splice donor site |
probably null |
|
|
R8006:Wwp1
|
UTSW |
4 |
19,650,174 (GRCm38) |
missense |
probably benign |
|
|
R8851:Wwp1
|
UTSW |
4 |
19,643,437 (GRCm38) |
missense |
probably null |
1.00 |
|
R8910:Wwp1
|
UTSW |
4 |
19,627,741 (GRCm38) |
missense |
possibly damaging |
0.70 |
|
R9020:Wwp1
|
UTSW |
4 |
19,650,282 (GRCm38) |
missense |
probably benign |
|
|
R9417:Wwp1
|
UTSW |
4 |
19,662,215 (GRCm38) |
missense |
possibly damaging |
0.67 |
|
R9736:Wwp1
|
UTSW |
4 |
19,631,202 (GRCm38) |
missense |
probably damaging |
0.99 |
|
X0018:Wwp1
|
UTSW |
4 |
19,640,261 (GRCm38) |
missense |
probably benign |
0.41 |
|
X0062:Wwp1
|
UTSW |
4 |
19,638,794 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
| Posted On |
2013-10-07 |
Incidental Mutation