Incidental Mutation 'R4909:Usp32'
| ID |
379314 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp32
|
| Ensembl Gene |
ENSMUSG00000000804 |
| Gene Name |
ubiquitin specific peptidase 32 |
| Synonyms |
2900074J03Rik, 6430526O11Rik |
| MMRRC Submission |
042511-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R4909 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
84875268-85030987 bp(-) (GRCm39) |
| Type of Mutation |
nonsense |
| DNA Base Change (assembly) |
G to A
at 84946598 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Glutamine to Stop codon
at position 269
(Q269*)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000103710
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108075]
|
| AlphaFold |
F8VPZ3 |
| Predicted Effect |
probably null
Transcript: ENSMUST00000108075
AA Change: Q269*
|
| SMART Domains |
Protein: ENSMUSP00000103710
Gene: ENSMUSG00000000804
AA Change: Q269*
| 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 |
noncoding transcript
Transcript: ENSMUST00000172950
|
| Meta Mutation Damage Score |
0.9755 |
| Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.3%
- 10x: 96.1%
- 20x: 91.7%
|
| Validation Efficiency |
97% (101/104) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 92 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1700030C10Rik |
A |
T |
12: 20,865,089 (GRCm39) |
|
noncoding transcript |
Het |
| Aars1 |
G |
A |
8: 111,781,715 (GRCm39) |
G929D |
probably damaging |
Het |
| Ablim2 |
C |
T |
5: 35,959,766 (GRCm39) |
R73C |
possibly damaging |
Het |
| Actn4 |
A |
T |
7: 28,598,082 (GRCm39) |
L506Q |
probably damaging |
Het |
| Adam26a |
A |
T |
8: 44,023,475 (GRCm39) |
F5Y |
probably benign |
Het |
| Adamts5 |
G |
A |
16: 85,696,954 (GRCm39) |
Q68* |
probably null |
Het |
| Adcy9 |
A |
G |
16: 4,116,618 (GRCm39) |
I871T |
probably benign |
Het |
| Ak5 |
A |
T |
3: 152,361,514 (GRCm39) |
L136H |
probably damaging |
Het |
| Ap1g2 |
A |
G |
14: 55,342,483 (GRCm39) |
|
probably null |
Het |
| Ap2a1 |
G |
A |
7: 44,555,805 (GRCm39) |
T355M |
probably damaging |
Het |
| Ap3s2 |
T |
C |
7: 79,564,989 (GRCm39) |
D60G |
possibly damaging |
Het |
| Apold1 |
G |
A |
6: 134,960,558 (GRCm39) |
R4Q |
probably benign |
Het |
| Atp13a5 |
G |
T |
16: 29,152,846 (GRCm39) |
Q207K |
possibly damaging |
Het |
| BC035947 |
A |
C |
1: 78,474,666 (GRCm39) |
I622S |
probably damaging |
Het |
| Bmper |
G |
T |
9: 23,289,021 (GRCm39) |
V339F |
probably benign |
Het |
| Btbd8 |
C |
T |
5: 107,655,176 (GRCm39) |
Q992* |
probably null |
Het |
| C1ra |
A |
G |
6: 124,499,293 (GRCm39) |
D493G |
probably damaging |
Het |
| C3 |
C |
T |
17: 57,533,830 (GRCm39) |
|
probably null |
Het |
| Cabp4 |
T |
A |
19: 4,187,120 (GRCm39) |
I209F |
possibly damaging |
Het |
| Cacna1s |
A |
T |
1: 136,007,342 (GRCm39) |
H453L |
probably damaging |
Het |
| Camk2g |
A |
G |
14: 20,842,652 (GRCm39) |
V32A |
probably benign |
Het |
| Ccdc175 |
G |
A |
12: 72,206,527 (GRCm39) |
R240C |
probably damaging |
Het |
| Cdk13 |
C |
T |
13: 17,946,988 (GRCm39) |
S590N |
possibly damaging |
Het |
| Cfap45 |
A |
T |
1: 172,357,443 (GRCm39) |
T24S |
probably benign |
Het |
| Clca3a1 |
T |
G |
3: 144,730,324 (GRCm39) |
K174Q |
probably damaging |
Het |
| Col1a2 |
G |
A |
6: 4,529,058 (GRCm39) |
|
probably benign |
Het |
| Colgalt1 |
A |
T |
8: 72,073,277 (GRCm39) |
I323F |
possibly damaging |
Het |
| Cpeb3 |
A |
T |
19: 37,152,059 (GRCm39) |
S106T |
probably damaging |
Het |
| Cpeb3 |
T |
C |
19: 37,151,633 (GRCm39) |
S248G |
possibly damaging |
Het |
| Ctcfl |
C |
T |
2: 172,937,191 (GRCm39) |
A576T |
probably benign |
Het |
| Cyp4f16 |
T |
G |
17: 32,769,295 (GRCm39) |
V395G |
possibly damaging |
Het |
| Dchs1 |
C |
T |
7: 105,415,462 (GRCm39) |
G605S |
probably damaging |
Het |
| Egflam |
A |
T |
15: 7,249,110 (GRCm39) |
F903I |
probably damaging |
Het |
| Eif5a |
G |
A |
11: 69,808,311 (GRCm39) |
A62V |
possibly damaging |
Het |
| Fam217a |
A |
G |
13: 35,094,389 (GRCm39) |
S609P |
probably damaging |
Het |
| Fhad1 |
T |
A |
4: 141,712,822 (GRCm39) |
I206F |
probably benign |
Het |
| Flt1 |
C |
A |
5: 147,620,749 (GRCm39) |
A132S |
probably benign |
Het |
| Fras1 |
T |
A |
5: 96,856,617 (GRCm39) |
M2000K |
probably benign |
Het |
| Frmd5 |
C |
T |
2: 121,422,134 (GRCm39) |
|
probably null |
Het |
| Gle1 |
T |
C |
2: 29,826,092 (GRCm39) |
L57P |
probably benign |
Het |
| Glrx3 |
C |
A |
7: 137,046,765 (GRCm39) |
N52K |
probably damaging |
Het |
| Grin3b |
A |
G |
10: 79,812,938 (GRCm39) |
*1004W |
probably null |
Het |
| Hectd4 |
T |
A |
5: 121,401,954 (GRCm39) |
F347L |
probably benign |
Het |
| Htra1 |
G |
A |
7: 130,586,802 (GRCm39) |
V462I |
probably benign |
Het |
| Itga11 |
A |
G |
9: 62,662,581 (GRCm39) |
Y518C |
probably damaging |
Het |
| Krtap15-1 |
T |
C |
16: 88,626,253 (GRCm39) |
F88L |
probably benign |
Het |
| Ktn1 |
A |
T |
14: 47,943,917 (GRCm39) |
R866W |
probably damaging |
Het |
| Lamb1 |
G |
A |
12: 31,338,280 (GRCm39) |
R483H |
probably damaging |
Het |
| Megf6 |
C |
T |
4: 154,349,848 (GRCm39) |
R983C |
probably damaging |
Het |
| Mybpc3 |
T |
A |
2: 90,965,157 (GRCm39) |
D1075E |
probably benign |
Het |
| Myo7b |
A |
T |
18: 32,097,489 (GRCm39) |
N1792K |
probably benign |
Het |
| Nabp2 |
A |
T |
10: 128,237,556 (GRCm39) |
|
probably benign |
Het |
| Neil3 |
A |
G |
8: 54,091,928 (GRCm39) |
C7R |
probably damaging |
Het |
| Nxpe2 |
T |
A |
9: 48,230,897 (GRCm39) |
I491F |
possibly damaging |
Het |
| Obscn |
A |
G |
11: 58,952,291 (GRCm39) |
V4292A |
possibly damaging |
Het |
| Ogfod3 |
A |
G |
11: 121,088,318 (GRCm39) |
S139P |
probably damaging |
Het |
| Oog2 |
T |
C |
4: 143,921,669 (GRCm39) |
I211T |
possibly damaging |
Het |
| Oosp1 |
T |
C |
19: 11,666,080 (GRCm39) |
D70G |
probably benign |
Het |
| Or10j2 |
A |
T |
1: 173,098,546 (GRCm39) |
D268V |
probably damaging |
Het |
| Or1ab2 |
A |
G |
8: 72,863,425 (GRCm39) |
N5S |
probably damaging |
Het |
| Or56a42-ps1 |
C |
A |
7: 104,777,435 (GRCm39) |
V70L |
probably benign |
Het |
| Or6c210 |
A |
G |
10: 129,496,589 (GRCm39) |
I305V |
probably benign |
Het |
| Padi3 |
T |
C |
4: 140,522,937 (GRCm39) |
D345G |
probably damaging |
Het |
| Pcyt2 |
A |
G |
11: 120,506,246 (GRCm39) |
F71L |
probably benign |
Het |
| Pi4k2b |
T |
C |
5: 52,911,971 (GRCm39) |
|
probably benign |
Het |
| Pigr |
A |
C |
1: 130,776,195 (GRCm39) |
T577P |
possibly damaging |
Het |
| Pirb |
G |
A |
7: 3,722,361 (GRCm39) |
Q161* |
probably null |
Het |
| Pnlip |
A |
G |
19: 58,664,672 (GRCm39) |
E204G |
possibly damaging |
Het |
| Pop7 |
G |
T |
5: 137,500,161 (GRCm39) |
D57E |
probably benign |
Het |
| Ppfia4 |
A |
T |
1: 134,260,239 (GRCm39) |
I8N |
probably damaging |
Het |
| Pprc1 |
A |
G |
19: 46,052,758 (GRCm39) |
T759A |
probably damaging |
Het |
| Prom1 |
T |
C |
5: 44,202,894 (GRCm39) |
N213S |
probably benign |
Het |
| Prop1 |
GCTTCACT |
GCTTCACTTCACT |
11: 50,842,863 (GRCm39) |
|
probably null |
Het |
| Prop1 |
A |
T |
11: 50,842,872 (GRCm39) |
L105H |
probably damaging |
Het |
| Pwp2 |
A |
T |
10: 78,018,328 (GRCm39) |
M121K |
possibly damaging |
Het |
| Rap1gds1 |
A |
T |
3: 138,689,509 (GRCm39) |
M161K |
possibly damaging |
Het |
| Rps6kb2 |
T |
A |
19: 4,207,002 (GRCm39) |
|
probably benign |
Het |
| Rxfp1 |
A |
G |
3: 79,552,109 (GRCm39) |
S731P |
probably benign |
Het |
| Scfd1 |
T |
C |
12: 51,437,195 (GRCm39) |
V137A |
probably benign |
Het |
| Slc6a15 |
G |
A |
10: 103,240,275 (GRCm39) |
D333N |
probably damaging |
Het |
| Sqor |
T |
C |
2: 122,627,101 (GRCm39) |
V74A |
possibly damaging |
Het |
| Stil |
T |
A |
4: 114,881,422 (GRCm39) |
Y655* |
probably null |
Het |
| Syt14 |
A |
T |
1: 192,581,167 (GRCm39) |
I468K |
probably damaging |
Het |
| Tbc1d31 |
T |
C |
15: 57,825,661 (GRCm39) |
|
probably null |
Het |
| Tspyl5 |
A |
T |
15: 33,686,995 (GRCm39) |
S317T |
probably damaging |
Het |
| Ttf1 |
C |
T |
2: 28,954,668 (GRCm39) |
H11Y |
possibly damaging |
Het |
| Ttf2 |
T |
C |
3: 100,861,631 (GRCm39) |
T620A |
probably damaging |
Het |
| Vsig10 |
T |
A |
5: 117,476,308 (GRCm39) |
V254E |
probably benign |
Het |
| Wdr6 |
C |
T |
9: 108,450,187 (GRCm39) |
A1114T |
probably benign |
Het |
| Zfp280d |
A |
G |
9: 72,238,714 (GRCm39) |
S63G |
probably damaging |
Het |
| Zfp607b |
A |
G |
7: 27,403,221 (GRCm39) |
D559G |
probably benign |
Het |
| Zfp934 |
T |
C |
13: 62,665,768 (GRCm39) |
H291R |
probably damaging |
Het |
|
| Other mutations in Usp32 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00529:Usp32
|
APN |
11 |
84,885,252 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL00701:Usp32
|
APN |
11 |
84,949,951 (GRCm39) |
splice site |
probably null |
|
|
IGL00848:Usp32
|
APN |
11 |
84,942,007 (GRCm39) |
splice site |
probably benign |
|
|
IGL00934:Usp32
|
APN |
11 |
84,897,902 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01019:Usp32
|
APN |
11 |
84,930,091 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL01302:Usp32
|
APN |
11 |
84,879,308 (GRCm39) |
missense |
probably benign |
0.05 |
|
IGL01444:Usp32
|
APN |
11 |
84,949,990 (GRCm39) |
missense |
probably damaging |
0.97 |
|
IGL01575:Usp32
|
APN |
11 |
84,913,628 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01981:Usp32
|
APN |
11 |
84,927,350 (GRCm39) |
missense |
probably benign |
0.02 |
|
IGL02118:Usp32
|
APN |
11 |
84,923,003 (GRCm39) |
nonsense |
probably null |
|
|
IGL02159:Usp32
|
APN |
11 |
84,896,628 (GRCm39) |
splice site |
probably null |
|
|
IGL02227:Usp32
|
APN |
11 |
84,877,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02363:Usp32
|
APN |
11 |
84,935,613 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL02524:Usp32
|
APN |
11 |
84,900,837 (GRCm39) |
nonsense |
probably null |
|
|
IGL02613:Usp32
|
APN |
11 |
84,930,896 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL02720:Usp32
|
APN |
11 |
84,897,817 (GRCm39) |
critical splice donor site |
probably null |
|
|
IGL02738:Usp32
|
APN |
11 |
84,974,632 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02929:Usp32
|
APN |
11 |
84,879,198 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03303:Usp32
|
APN |
11 |
84,913,658 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB010:Usp32
|
UTSW |
11 |
84,897,885 (GRCm39) |
missense |
probably damaging |
1.00 |
|
BB020:Usp32
|
UTSW |
11 |
84,897,885 (GRCm39) |
missense |
probably damaging |
1.00 |
|
PIT4812001:Usp32
|
UTSW |
11 |
84,900,900 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0026:Usp32
|
UTSW |
11 |
84,922,900 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R0295:Usp32
|
UTSW |
11 |
84,944,518 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1320:Usp32
|
UTSW |
11 |
84,908,619 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1712:Usp32
|
UTSW |
11 |
84,933,406 (GRCm39) |
missense |
probably benign |
0.12 |
|
R1922:Usp32
|
UTSW |
11 |
84,897,830 (GRCm39) |
nonsense |
probably null |
|
|
R1973:Usp32
|
UTSW |
11 |
84,994,757 (GRCm39) |
missense |
probably benign |
0.09 |
|
R2010:Usp32
|
UTSW |
11 |
84,930,830 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2082:Usp32
|
UTSW |
11 |
84,921,338 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R2355:Usp32
|
UTSW |
11 |
84,896,735 (GRCm39) |
missense |
probably benign |
0.34 |
|
R3147:Usp32
|
UTSW |
11 |
84,919,913 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3160:Usp32
|
UTSW |
11 |
84,916,362 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R3162:Usp32
|
UTSW |
11 |
84,916,362 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R3716:Usp32
|
UTSW |
11 |
84,933,389 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3816:Usp32
|
UTSW |
11 |
84,885,210 (GRCm39) |
critical splice donor site |
probably null |
|
|
R3870:Usp32
|
UTSW |
11 |
84,897,881 (GRCm39) |
nonsense |
probably null |
|
|
R3871:Usp32
|
UTSW |
11 |
84,971,982 (GRCm39) |
missense |
probably null |
0.81 |
|
R4041:Usp32
|
UTSW |
11 |
84,908,565 (GRCm39) |
missense |
probably benign |
0.40 |
|
R4079:Usp32
|
UTSW |
11 |
84,930,055 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R4332:Usp32
|
UTSW |
11 |
84,994,804 (GRCm39) |
missense |
possibly damaging |
0.79 |
|
R4396:Usp32
|
UTSW |
11 |
84,944,801 (GRCm39) |
missense |
probably benign |
|
|
R4580:Usp32
|
UTSW |
11 |
84,949,953 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4620:Usp32
|
UTSW |
11 |
84,949,953 (GRCm39) |
critical splice donor site |
probably null |
|
|
R4744:Usp32
|
UTSW |
11 |
84,885,219 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5056:Usp32
|
UTSW |
11 |
84,917,621 (GRCm39) |
missense |
probably benign |
0.07 |
|
R5111:Usp32
|
UTSW |
11 |
84,968,157 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
R5213:Usp32
|
UTSW |
11 |
84,913,085 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5308:Usp32
|
UTSW |
11 |
84,908,544 (GRCm39) |
missense |
probably benign |
0.12 |
|
R5381:Usp32
|
UTSW |
11 |
84,949,953 (GRCm39) |
critical splice donor site |
probably benign |
|
|
R5538:Usp32
|
UTSW |
11 |
84,908,612 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R5659:Usp32
|
UTSW |
11 |
84,968,240 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6006:Usp32
|
UTSW |
11 |
84,883,277 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6011:Usp32
|
UTSW |
11 |
84,922,923 (GRCm39) |
missense |
possibly damaging |
0.70 |
|
R6029:Usp32
|
UTSW |
11 |
84,916,408 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6074:Usp32
|
UTSW |
11 |
84,885,399 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6331:Usp32
|
UTSW |
11 |
84,877,402 (GRCm39) |
missense |
possibly damaging |
0.92 |
|
R6353:Usp32
|
UTSW |
11 |
84,913,107 (GRCm39) |
missense |
probably benign |
|
|
R6714:Usp32
|
UTSW |
11 |
84,917,696 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R6778:Usp32
|
UTSW |
11 |
84,916,512 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6988:Usp32
|
UTSW |
11 |
84,900,969 (GRCm39) |
missense |
probably benign |
0.35 |
|
R6992:Usp32
|
UTSW |
11 |
84,922,914 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7182:Usp32
|
UTSW |
11 |
84,930,996 (GRCm39) |
missense |
probably benign |
0.34 |
|
R7186:Usp32
|
UTSW |
11 |
84,942,060 (GRCm39) |
missense |
probably benign |
0.45 |
|
R7198:Usp32
|
UTSW |
11 |
84,913,681 (GRCm39) |
frame shift |
probably null |
|
|
R7201:Usp32
|
UTSW |
11 |
84,913,681 (GRCm39) |
frame shift |
probably null |
|
|
R7469:Usp32
|
UTSW |
11 |
84,879,379 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7502:Usp32
|
UTSW |
11 |
84,913,724 (GRCm39) |
missense |
possibly damaging |
0.48 |
|
R7513:Usp32
|
UTSW |
11 |
84,917,938 (GRCm39) |
nonsense |
probably null |
|
|
R7629:Usp32
|
UTSW |
11 |
84,910,681 (GRCm39) |
frame shift |
probably null |
|
|
R7703:Usp32
|
UTSW |
11 |
84,968,153 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7741:Usp32
|
UTSW |
11 |
84,878,107 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7765:Usp32
|
UTSW |
11 |
84,885,234 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7933:Usp32
|
UTSW |
11 |
84,897,885 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7973:Usp32
|
UTSW |
11 |
84,913,634 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R7989:Usp32
|
UTSW |
11 |
84,925,126 (GRCm39) |
missense |
|
|
|
R7998:Usp32
|
UTSW |
11 |
84,885,252 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8292:Usp32
|
UTSW |
11 |
84,968,227 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R8305:Usp32
|
UTSW |
11 |
84,923,011 (GRCm39) |
missense |
possibly damaging |
0.83 |
|
R8548:Usp32
|
UTSW |
11 |
84,908,653 (GRCm39) |
missense |
possibly damaging |
0.52 |
|
R8924:Usp32
|
UTSW |
11 |
84,916,370 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9002:Usp32
|
UTSW |
11 |
84,944,777 (GRCm39) |
missense |
probably damaging |
0.96 |
|
R9145:Usp32
|
UTSW |
11 |
84,913,118 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9209:Usp32
|
UTSW |
11 |
84,930,838 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R9211:Usp32
|
UTSW |
11 |
84,913,559 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9296:Usp32
|
UTSW |
11 |
84,908,478 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9310:Usp32
|
UTSW |
11 |
84,942,028 (GRCm39) |
missense |
probably benign |
0.29 |
|
R9417:Usp32
|
UTSW |
11 |
84,885,369 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9514:Usp32
|
UTSW |
11 |
84,913,560 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R9652:Usp32
|
UTSW |
11 |
84,921,317 (GRCm39) |
missense |
probably damaging |
0.97 |
|
R9723:Usp32
|
UTSW |
11 |
84,935,536 (GRCm39) |
nonsense |
probably null |
|
|
R9757:Usp32
|
UTSW |
11 |
84,968,155 (GRCm39) |
nonsense |
probably null |
|
|
X0028:Usp32
|
UTSW |
11 |
84,883,432 (GRCm39) |
missense |
probably benign |
0.05 |
|
Z1177:Usp32
|
UTSW |
11 |
84,879,438 (GRCm39) |
nonsense |
probably null |
|
|
| Predicted Primers |
PCR Primer
(F):5'- CTTAAAAGAATCCAAACTAGGTTGATG -3'
(R):5'- AGAGACATTCTTGACTTCATAAACGT -3'
Sequencing Primer
(F):5'- GAATCCAAACTAGGTTGATGCTTCC -3'
(R):5'- GCTTTTGATGAAAATCGTGA -3'
|
| Posted On |
2016-04-15 |
Incidental Mutation