Incidental Mutation 'R1712:Usp32'
| ID |
190693 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp32
|
| Ensembl Gene |
ENSMUSG00000000804 |
| Gene Name |
ubiquitin specific peptidase 32 |
| Synonyms |
6430526O11Rik, 2900074J03Rik |
| MMRRC Submission |
039745-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R1712 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
84984442-85140161 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to T
at 85042580 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Isoleucine to Asparagine
at position 34
(I34N)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000133781
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108075]
[ENSMUST00000172515]
|
| AlphaFold |
F8VPZ3 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000108075
AA Change: I447N
PolyPhen 2
Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
|
| SMART Domains |
Protein: ENSMUSP00000103710
Gene: ENSMUSG00000000804
AA Change: I447N
| Domain | Start | End | E-Value | Type |
|---|
|
EFh
|
232 |
260 |
4.66e0 |
SMART |
|
EFh
|
268 |
296 |
5.8e-1 |
SMART |
|
Blast:EFh
|
318 |
346 |
5e-7 |
BLAST |
|
DUSP
|
389 |
588 |
2.32e-16 |
SMART |
|
Pfam:Ubiquitin_3
|
628 |
711 |
2.4e-9 |
PFAM |
|
Pfam:UCH
|
733 |
1564 |
2.4e-83 |
PFAM |
|
Pfam:UCH_1
|
1202 |
1547 |
2.9e-12 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000172515
AA Change: I34N
PolyPhen 2
Score 0.122 (Sensitivity: 0.93; Specificity: 0.86)
|
| SMART Domains |
Protein: ENSMUSP00000133781
Gene: ENSMUSG00000000804
AA Change: I34N
| Domain | Start | End | E-Value | Type |
|---|
|
Blast:DUSP
|
1 |
52 |
7e-30 |
BLAST |
|
low complexity region
|
53 |
65 |
N/A |
INTRINSIC |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000174602
|
| SMART Domains |
Protein: ENSMUSP00000134476
Gene: ENSMUSG00000000804
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:DUSP
|
1 |
65 |
6.5e-17 |
PFAM |
|
Pfam:Ubiquitin_3
|
122 |
216 |
8e-10 |
PFAM |
|
Pfam:UCH
|
238 |
257 |
1.2e-7 |
PFAM |
|
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.4%
- 10x: 96.5%
- 20x: 93.2%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 83 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Accs |
T |
A |
2: 93,848,103 (GRCm38) |
E12D |
probably damaging |
Het |
| Ahnak2 |
C |
A |
12: 112,785,378 (GRCm38) |
R283L |
probably benign |
Het |
| BC005624 |
T |
C |
2: 30,974,008 (GRCm38) |
E191G |
probably damaging |
Het |
| C1galt1 |
A |
G |
6: 7,871,217 (GRCm38) |
N351S |
probably benign |
Het |
| Ccdc162 |
T |
C |
10: 41,539,431 (GRCm38) |
R2179G |
probably benign |
Het |
| Ccdc88c |
G |
A |
12: 100,939,025 (GRCm38) |
T1108M |
probably benign |
Het |
| Cd47 |
T |
C |
16: 49,894,180 (GRCm38) |
L184P |
probably damaging |
Het |
| Cdc40 |
T |
C |
10: 40,841,376 (GRCm38) |
K440E |
probably damaging |
Het |
| Cenpe |
G |
A |
3: 135,265,933 (GRCm38) |
V2262I |
probably damaging |
Het |
| Cep290 |
A |
G |
10: 100,554,499 (GRCm38) |
K2035E |
probably benign |
Het |
| Cks1brt |
G |
T |
8: 85,171,543 (GRCm38) |
L8F |
probably benign |
Het |
| Col17a1 |
T |
C |
19: 47,649,003 (GRCm38) |
|
probably benign |
Het |
| Coro6 |
A |
T |
11: 77,469,467 (GRCm38) |
N421I |
probably benign |
Het |
| Cps1 |
T |
C |
1: 67,230,281 (GRCm38) |
S1480P |
probably damaging |
Het |
| Csrnp3 |
G |
T |
2: 66,002,482 (GRCm38) |
A110S |
probably damaging |
Het |
| Cyp2d10 |
G |
T |
15: 82,403,039 (GRCm38) |
T461K |
probably damaging |
Het |
| Dmxl2 |
A |
G |
9: 54,401,485 (GRCm38) |
V1994A |
probably benign |
Het |
| Dnah11 |
T |
A |
12: 118,196,644 (GRCm38) |
N117I |
probably benign |
Het |
| Dnajc3 |
A |
G |
14: 118,957,895 (GRCm38) |
Y74C |
probably damaging |
Het |
| Fam13c |
T |
A |
10: 70,554,573 (GRCm38) |
F555I |
possibly damaging |
Het |
| Fbn1 |
T |
A |
2: 125,346,434 (GRCm38) |
D1495V |
probably damaging |
Het |
| Fbrsl1 |
T |
C |
5: 110,447,996 (GRCm38) |
T58A |
probably benign |
Het |
| Gjc1 |
A |
G |
11: 102,800,880 (GRCm38) |
I99T |
possibly damaging |
Het |
| Glce |
T |
C |
9: 62,070,575 (GRCm38) |
N9S |
probably damaging |
Het |
| Gosr1 |
T |
C |
11: 76,750,878 (GRCm38) |
T125A |
possibly damaging |
Het |
| Ifi27 |
T |
A |
12: 103,439,943 (GRCm38) |
|
probably null |
Het |
| Jph1 |
C |
T |
1: 17,097,232 (GRCm38) |
D125N |
possibly damaging |
Het |
| Kbtbd12 |
A |
T |
6: 88,618,694 (GRCm38) |
S51R |
probably damaging |
Het |
| Klra9 |
A |
T |
6: 130,189,696 (GRCm38) |
|
probably null |
Het |
| Kmo |
A |
T |
1: 175,656,723 (GRCm38) |
M340L |
probably benign |
Het |
| Lama1 |
T |
C |
17: 67,717,186 (GRCm38) |
I93T |
possibly damaging |
Het |
| Limk2 |
A |
T |
11: 3,358,104 (GRCm38) |
|
probably null |
Het |
| Mgat5 |
C |
A |
1: 127,320,638 (GRCm38) |
N92K |
probably benign |
Het |
| Mib2 |
T |
A |
4: 155,654,799 (GRCm38) |
I908F |
probably damaging |
Het |
| Mical1 |
T |
G |
10: 41,480,363 (GRCm38) |
L304R |
probably damaging |
Het |
| Mtbp |
G |
T |
15: 55,571,294 (GRCm38) |
|
probably null |
Het |
| Myo3a |
T |
C |
2: 22,564,992 (GRCm38) |
Y70H |
probably damaging |
Het |
| Neb |
T |
C |
2: 52,243,389 (GRCm38) |
Y3379C |
probably damaging |
Het |
| Neurod2 |
G |
T |
11: 98,327,203 (GRCm38) |
N378K |
probably damaging |
Het |
| Olfr1051 |
T |
A |
2: 86,275,993 (GRCm38) |
T165S |
probably damaging |
Het |
| Olfr117 |
A |
G |
17: 37,659,908 (GRCm38) |
S142P |
probably benign |
Het |
| Olfr1286 |
T |
A |
2: 111,420,658 (GRCm38) |
M98L |
probably benign |
Het |
| Olfr986 |
A |
G |
9: 40,187,865 (GRCm38) |
Y250C |
probably damaging |
Het |
| Oog4 |
G |
A |
4: 143,439,914 (GRCm38) |
L107F |
probably damaging |
Het |
| Pfdn6 |
T |
C |
17: 33,939,554 (GRCm38) |
Y82C |
probably damaging |
Het |
| Pla2g4d |
C |
A |
2: 120,277,490 (GRCm38) |
A313S |
possibly damaging |
Het |
| Ptcd3 |
C |
A |
6: 71,908,653 (GRCm38) |
E30* |
probably null |
Het |
| Rai1 |
A |
G |
11: 60,187,602 (GRCm38) |
T831A |
probably benign |
Het |
| Rims1 |
G |
A |
1: 22,296,948 (GRCm38) |
T1176M |
probably damaging |
Het |
| Rin1 |
A |
C |
19: 5,055,143 (GRCm38) |
I744L |
probably benign |
Het |
| Rora |
T |
A |
9: 69,375,489 (GRCm38) |
S430T |
probably benign |
Het |
| Rsph10b |
T |
A |
5: 143,937,149 (GRCm38) |
S23T |
probably damaging |
Het |
| Ryr1 |
T |
C |
7: 29,047,503 (GRCm38) |
N3773S |
probably benign |
Het |
| Scn4a |
C |
A |
11: 106,345,547 (GRCm38) |
G296C |
probably benign |
Het |
| Scn4a |
A |
G |
11: 106,339,354 (GRCm38) |
Y543H |
probably damaging |
Het |
| Scn7a |
T |
C |
2: 66,705,103 (GRCm38) |
T435A |
probably benign |
Het |
| Shank2 |
G |
T |
7: 144,411,153 (GRCm38) |
D833Y |
probably damaging |
Het |
| Slc9a2 |
T |
C |
1: 40,763,610 (GRCm38) |
S607P |
possibly damaging |
Het |
| Slx4 |
G |
A |
16: 3,991,594 (GRCm38) |
R346W |
probably damaging |
Het |
| Spata20 |
A |
T |
11: 94,480,514 (GRCm38) |
C675S |
probably benign |
Het |
| Suclg2 |
A |
T |
6: 95,587,016 (GRCm38) |
I196N |
probably damaging |
Het |
| Sv2b |
G |
A |
7: 75,149,059 (GRCm38) |
H272Y |
possibly damaging |
Het |
| Svep1 |
T |
C |
4: 58,070,629 (GRCm38) |
I2386V |
probably benign |
Het |
| Taf13 |
A |
T |
3: 108,581,129 (GRCm38) |
E109D |
possibly damaging |
Het |
| Tanc2 |
A |
G |
11: 105,899,780 (GRCm38) |
T976A |
probably benign |
Het |
| Tax1bp1 |
A |
G |
6: 52,729,326 (GRCm38) |
Y104C |
probably damaging |
Het |
| Tfeb |
T |
C |
17: 47,788,986 (GRCm38) |
|
probably null |
Het |
| Tlr9 |
T |
C |
9: 106,224,049 (GRCm38) |
Y180H |
probably damaging |
Het |
| Trappc9 |
G |
A |
15: 73,025,967 (GRCm38) |
R377W |
probably damaging |
Het |
| Ttc12 |
T |
A |
9: 49,445,199 (GRCm38) |
T510S |
probably benign |
Het |
| Ubqln1 |
T |
C |
13: 58,192,081 (GRCm38) |
E280G |
probably damaging |
Het |
| Urm1 |
T |
C |
2: 29,841,425 (GRCm38) |
W44R |
probably damaging |
Het |
| Vars |
T |
C |
17: 35,014,752 (GRCm38) |
L1018P |
probably damaging |
Het |
| Vcan |
A |
T |
13: 89,721,775 (GRCm38) |
V206D |
probably damaging |
Het |
| Vim |
T |
C |
2: 13,578,459 (GRCm38) |
V224A |
probably damaging |
Het |
| Vmn2r106 |
G |
T |
17: 20,278,735 (GRCm38) |
H305N |
probably benign |
Het |
| Vmn2r78 |
A |
G |
7: 86,954,924 (GRCm38) |
N770S |
probably damaging |
Het |
| Wdr33 |
T |
A |
18: 31,896,631 (GRCm38) |
L961Q |
unknown |
Het |
| Xylt2 |
A |
G |
11: 94,668,749 (GRCm38) |
S356P |
possibly damaging |
Het |
| Zbtb14 |
A |
G |
17: 69,387,580 (GRCm38) |
N91S |
probably damaging |
Het |
| Zc3h6 |
T |
C |
2: 129,016,734 (GRCm38) |
L895S |
probably damaging |
Het |
| Zc3h7b |
C |
T |
15: 81,777,088 (GRCm38) |
P376L |
probably benign |
Het |
| Zfp131 |
T |
C |
13: 119,766,543 (GRCm38) |
T523A |
probably benign |
Het |
|
| Other mutations in Usp32 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00529:Usp32
|
APN |
11 |
84,994,426 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL00701:Usp32
|
APN |
11 |
85,059,125 (GRCm38) |
splice site |
probably null |
|
|
IGL00848:Usp32
|
APN |
11 |
85,051,181 (GRCm38) |
splice site |
probably benign |
|
|
IGL00934:Usp32
|
APN |
11 |
85,007,076 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01019:Usp32
|
APN |
11 |
85,039,265 (GRCm38) |
missense |
probably damaging |
0.97 |
|
IGL01302:Usp32
|
APN |
11 |
84,988,482 (GRCm38) |
missense |
probably benign |
0.05 |
|
IGL01444:Usp32
|
APN |
11 |
85,059,164 (GRCm38) |
missense |
probably damaging |
0.97 |
|
IGL01575:Usp32
|
APN |
11 |
85,022,802 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL01981:Usp32
|
APN |
11 |
85,036,524 (GRCm38) |
missense |
probably benign |
0.02 |
|
IGL02118:Usp32
|
APN |
11 |
85,032,177 (GRCm38) |
nonsense |
probably null |
|
|
IGL02159:Usp32
|
APN |
11 |
85,005,802 (GRCm38) |
splice site |
probably null |
|
|
IGL02227:Usp32
|
APN |
11 |
84,986,481 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02363:Usp32
|
APN |
11 |
85,044,787 (GRCm38) |
missense |
probably benign |
0.01 |
|
IGL02524:Usp32
|
APN |
11 |
85,010,011 (GRCm38) |
nonsense |
probably null |
|
|
IGL02613:Usp32
|
APN |
11 |
85,040,070 (GRCm38) |
missense |
probably damaging |
0.99 |
|
IGL02720:Usp32
|
APN |
11 |
85,006,991 (GRCm38) |
critical splice donor site |
probably null |
|
|
IGL02738:Usp32
|
APN |
11 |
85,083,806 (GRCm38) |
missense |
probably damaging |
1.00 |
|
IGL02929:Usp32
|
APN |
11 |
84,988,372 (GRCm38) |
missense |
probably benign |
0.01 |
|
IGL03303:Usp32
|
APN |
11 |
85,022,832 (GRCm38) |
missense |
probably damaging |
1.00 |
|
BB010:Usp32
|
UTSW |
11 |
85,007,059 (GRCm38) |
missense |
probably damaging |
1.00 |
|
BB020:Usp32
|
UTSW |
11 |
85,007,059 (GRCm38) |
missense |
probably damaging |
1.00 |
|
PIT4812001:Usp32
|
UTSW |
11 |
85,010,074 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R0026:Usp32
|
UTSW |
11 |
85,032,074 (GRCm38) |
missense |
possibly damaging |
0.48 |
|
R0295:Usp32
|
UTSW |
11 |
85,053,692 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R1320:Usp32
|
UTSW |
11 |
85,017,793 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R1922:Usp32
|
UTSW |
11 |
85,007,004 (GRCm38) |
nonsense |
probably null |
|
|
R1973:Usp32
|
UTSW |
11 |
85,103,931 (GRCm38) |
missense |
probably benign |
0.09 |
|
R2010:Usp32
|
UTSW |
11 |
85,040,004 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R2082:Usp32
|
UTSW |
11 |
85,030,512 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R2355:Usp32
|
UTSW |
11 |
85,005,909 (GRCm38) |
missense |
probably benign |
0.34 |
|
R3147:Usp32
|
UTSW |
11 |
85,029,087 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3160:Usp32
|
UTSW |
11 |
85,025,536 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R3162:Usp32
|
UTSW |
11 |
85,025,536 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R3716:Usp32
|
UTSW |
11 |
85,042,563 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R3816:Usp32
|
UTSW |
11 |
84,994,384 (GRCm38) |
critical splice donor site |
probably null |
|
|
R3870:Usp32
|
UTSW |
11 |
85,007,055 (GRCm38) |
nonsense |
probably null |
|
|
R3871:Usp32
|
UTSW |
11 |
85,081,156 (GRCm38) |
missense |
probably null |
0.81 |
|
R4041:Usp32
|
UTSW |
11 |
85,017,739 (GRCm38) |
missense |
probably benign |
0.40 |
|
R4079:Usp32
|
UTSW |
11 |
85,039,229 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R4332:Usp32
|
UTSW |
11 |
85,103,978 (GRCm38) |
missense |
possibly damaging |
0.79 |
|
R4396:Usp32
|
UTSW |
11 |
85,053,975 (GRCm38) |
missense |
probably benign |
|
|
R4580:Usp32
|
UTSW |
11 |
85,059,127 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4620:Usp32
|
UTSW |
11 |
85,059,127 (GRCm38) |
critical splice donor site |
probably null |
|
|
R4744:Usp32
|
UTSW |
11 |
84,994,393 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R4909:Usp32
|
UTSW |
11 |
85,055,772 (GRCm38) |
nonsense |
probably null |
|
|
R5056:Usp32
|
UTSW |
11 |
85,026,795 (GRCm38) |
missense |
probably benign |
0.07 |
|
R5111:Usp32
|
UTSW |
11 |
85,077,331 (GRCm38) |
missense |
possibly damaging |
0.95 |
|
R5213:Usp32
|
UTSW |
11 |
85,022,259 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R5308:Usp32
|
UTSW |
11 |
85,017,718 (GRCm38) |
missense |
probably benign |
0.12 |
|
R5381:Usp32
|
UTSW |
11 |
85,059,127 (GRCm38) |
critical splice donor site |
probably benign |
|
|
R5538:Usp32
|
UTSW |
11 |
85,017,786 (GRCm38) |
missense |
possibly damaging |
0.65 |
|
R5659:Usp32
|
UTSW |
11 |
85,077,414 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R6006:Usp32
|
UTSW |
11 |
84,992,451 (GRCm38) |
critical splice donor site |
probably null |
|
|
R6011:Usp32
|
UTSW |
11 |
85,032,097 (GRCm38) |
missense |
possibly damaging |
0.70 |
|
R6029:Usp32
|
UTSW |
11 |
85,025,582 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R6074:Usp32
|
UTSW |
11 |
84,994,573 (GRCm38) |
missense |
probably benign |
0.00 |
|
R6331:Usp32
|
UTSW |
11 |
84,986,576 (GRCm38) |
missense |
possibly damaging |
0.92 |
|
R6353:Usp32
|
UTSW |
11 |
85,022,281 (GRCm38) |
missense |
probably benign |
|
|
R6714:Usp32
|
UTSW |
11 |
85,026,870 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R6778:Usp32
|
UTSW |
11 |
85,025,686 (GRCm38) |
missense |
probably benign |
0.00 |
|
R6988:Usp32
|
UTSW |
11 |
85,010,143 (GRCm38) |
missense |
probably benign |
0.35 |
|
R6992:Usp32
|
UTSW |
11 |
85,032,088 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7182:Usp32
|
UTSW |
11 |
85,040,170 (GRCm38) |
missense |
probably benign |
0.34 |
|
R7186:Usp32
|
UTSW |
11 |
85,051,234 (GRCm38) |
missense |
probably benign |
0.45 |
|
R7198:Usp32
|
UTSW |
11 |
85,022,855 (GRCm38) |
frame shift |
probably null |
|
|
R7201:Usp32
|
UTSW |
11 |
85,022,855 (GRCm38) |
frame shift |
probably null |
|
|
R7469:Usp32
|
UTSW |
11 |
84,988,553 (GRCm38) |
missense |
possibly damaging |
0.94 |
|
R7502:Usp32
|
UTSW |
11 |
85,022,898 (GRCm38) |
missense |
possibly damaging |
0.48 |
|
R7513:Usp32
|
UTSW |
11 |
85,027,112 (GRCm38) |
nonsense |
probably null |
|
|
R7629:Usp32
|
UTSW |
11 |
85,019,855 (GRCm38) |
frame shift |
probably null |
|
|
R7703:Usp32
|
UTSW |
11 |
85,077,327 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7741:Usp32
|
UTSW |
11 |
84,987,281 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7765:Usp32
|
UTSW |
11 |
84,994,408 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7933:Usp32
|
UTSW |
11 |
85,007,059 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R7973:Usp32
|
UTSW |
11 |
85,022,808 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R7989:Usp32
|
UTSW |
11 |
85,034,300 (GRCm38) |
missense |
|
|
|
R7998:Usp32
|
UTSW |
11 |
84,994,426 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R8292:Usp32
|
UTSW |
11 |
85,077,401 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R8305:Usp32
|
UTSW |
11 |
85,032,185 (GRCm38) |
missense |
possibly damaging |
0.83 |
|
R8548:Usp32
|
UTSW |
11 |
85,017,827 (GRCm38) |
missense |
possibly damaging |
0.52 |
|
R8924:Usp32
|
UTSW |
11 |
85,025,544 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R9002:Usp32
|
UTSW |
11 |
85,053,951 (GRCm38) |
missense |
probably damaging |
0.96 |
|
R9145:Usp32
|
UTSW |
11 |
85,022,292 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9209:Usp32
|
UTSW |
11 |
85,040,012 (GRCm38) |
missense |
probably damaging |
0.98 |
|
R9211:Usp32
|
UTSW |
11 |
85,022,733 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9296:Usp32
|
UTSW |
11 |
85,017,652 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9310:Usp32
|
UTSW |
11 |
85,051,202 (GRCm38) |
missense |
probably benign |
0.29 |
|
R9417:Usp32
|
UTSW |
11 |
84,994,543 (GRCm38) |
missense |
probably damaging |
1.00 |
|
R9514:Usp32
|
UTSW |
11 |
85,022,734 (GRCm38) |
missense |
probably damaging |
0.99 |
|
R9652:Usp32
|
UTSW |
11 |
85,030,491 (GRCm38) |
missense |
probably damaging |
0.97 |
|
R9723:Usp32
|
UTSW |
11 |
85,044,710 (GRCm38) |
nonsense |
probably null |
|
|
R9757:Usp32
|
UTSW |
11 |
85,077,329 (GRCm38) |
nonsense |
probably null |
|
|
X0028:Usp32
|
UTSW |
11 |
84,992,606 (GRCm38) |
missense |
probably benign |
0.05 |
|
Z1177:Usp32
|
UTSW |
11 |
84,988,612 (GRCm38) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- gctgtTGAGCCAGTCTGATGCAAA -3'
(R):5'- GGTCTTTTCTCAGTGCCCTGATGAGT -3'
Sequencing Primer
(F):5'- ccccaggaccacaggac -3'
(R):5'- tcaacagccttctctaacctac -3'
|
| Posted On |
2014-05-14 |
Incidental Mutation