Incidental Mutation 'R8924:Usp32'
| ID |
679483 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp32
|
| Ensembl Gene |
ENSMUSG00000000804 |
| Gene Name |
ubiquitin specific peptidase 32 |
| Synonyms |
2900074J03Rik, 6430526O11Rik |
| MMRRC Submission |
068769-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R8924 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
84875268-85030987 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 84916370 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Arginine to Glutamine
at position 858
(R858Q)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000103710
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108075]
|
| AlphaFold |
F8VPZ3 |
| Predicted Effect |
|
| SMART Domains |
Protein: ENSMUSP00000000821
Gene: ENSMUSG00000000804
AA Change: R156Q
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:UCH
|
32 |
260 |
4.1e-51 |
PFAM |
|
Pfam:UCH_1
|
33 |
228 |
1.7e-7 |
PFAM |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000108075
AA Change: R858Q
PolyPhen 2
Score 0.976 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000103710
Gene: ENSMUSG00000000804
AA Change: R858Q
| 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: 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: 100.0%
- 3x: 99.9%
- 10x: 99.7%
- 20x: 99.0%
|
| Validation Efficiency |
98% (88/90) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 90 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Abca8b |
A |
G |
11: 109,838,003 (GRCm39) |
V1145A |
probably benign |
Het |
| Ank1 |
T |
C |
8: 23,589,011 (GRCm39) |
M562T |
probably benign |
Het |
| Atn1 |
A |
T |
6: 124,722,211 (GRCm39) |
S881T |
probably benign |
Het |
| B3galt1 |
C |
T |
2: 67,949,059 (GRCm39) |
T258I |
probably benign |
Het |
| Bahcc1 |
C |
T |
11: 120,167,591 (GRCm39) |
L1331F |
probably benign |
Het |
| Capn12 |
G |
A |
7: 28,582,628 (GRCm39) |
V168M |
probably damaging |
Het |
| Card14 |
T |
C |
11: 119,216,930 (GRCm39) |
V338A |
possibly damaging |
Het |
| Cd27 |
T |
C |
6: 125,213,432 (GRCm39) |
|
probably benign |
Het |
| Cd37 |
A |
G |
7: 44,888,109 (GRCm39) |
L37P |
probably damaging |
Het |
| Cd96 |
A |
G |
16: 45,919,385 (GRCm39) |
L212P |
probably damaging |
Het |
| Celsr1 |
T |
C |
15: 85,916,671 (GRCm39) |
E434G |
possibly damaging |
Het |
| Cep152 |
A |
G |
2: 125,444,778 (GRCm39) |
M456T |
possibly damaging |
Het |
| Ces3b |
G |
A |
8: 105,811,619 (GRCm39) |
R45H |
probably benign |
Het |
| Cfap54 |
T |
G |
10: 92,837,685 (GRCm39) |
T1072P |
probably damaging |
Het |
| Chodl |
A |
T |
16: 78,738,659 (GRCm39) |
M172L |
possibly damaging |
Het |
| Cilp2 |
A |
G |
8: 70,339,108 (GRCm39) |
S47P |
probably damaging |
Het |
| Clasrp |
T |
C |
7: 19,318,232 (GRCm39) |
I596V |
unknown |
Het |
| Clcn2 |
C |
T |
16: 20,530,930 (GRCm39) |
V267I |
probably damaging |
Het |
| Cntln |
T |
A |
4: 84,806,936 (GRCm39) |
D139E |
probably damaging |
Het |
| Cyp2j12 |
A |
C |
4: 95,994,685 (GRCm39) |
N379K |
probably damaging |
Het |
| Defb21 |
T |
C |
2: 152,416,704 (GRCm39) |
V60A |
possibly damaging |
Het |
| Dnajc16 |
G |
T |
4: 141,494,018 (GRCm39) |
S543* |
probably null |
Het |
| Efcab12 |
G |
T |
6: 115,800,664 (GRCm39) |
H120N |
probably benign |
Het |
| Efcab3 |
AACTCTA |
AA |
11: 104,806,253 (GRCm39) |
|
probably null |
Het |
| Efl1 |
G |
A |
7: 82,412,161 (GRCm39) |
G850D |
probably benign |
Het |
| Efna1 |
T |
C |
3: 89,183,635 (GRCm39) |
M64V |
probably benign |
Het |
| Eif2ak3 |
T |
C |
6: 70,870,003 (GRCm39) |
W897R |
probably damaging |
Het |
| Eif2ak4 |
T |
A |
2: 118,258,513 (GRCm39) |
F621Y |
probably damaging |
Het |
| Erbin |
C |
A |
13: 103,975,966 (GRCm39) |
E643* |
probably null |
Het |
| Esr1 |
G |
A |
10: 4,807,176 (GRCm39) |
W364* |
probably null |
Het |
| Fam171a2 |
T |
C |
11: 102,330,861 (GRCm39) |
E206G |
possibly damaging |
Het |
| Fam90a1a |
T |
C |
8: 22,451,429 (GRCm39) |
F97L |
probably benign |
Het |
| Fap |
A |
T |
2: 62,378,165 (GRCm39) |
F181I |
probably benign |
Het |
| Fem1b |
T |
C |
9: 62,704,916 (GRCm39) |
N115D |
probably damaging |
Het |
| Gal3st2b |
G |
T |
1: 93,868,653 (GRCm39) |
A295S |
probably benign |
Het |
| Galnt10 |
G |
A |
11: 57,674,681 (GRCm39) |
|
probably benign |
Het |
| Gcfc2 |
T |
C |
6: 81,909,879 (GRCm39) |
V224A |
probably damaging |
Het |
| Gh |
T |
C |
11: 106,191,634 (GRCm39) |
E136G |
probably damaging |
Het |
| Gjd3 |
C |
T |
11: 98,873,325 (GRCm39) |
C173Y |
probably damaging |
Het |
| Gm12695 |
T |
A |
4: 96,651,046 (GRCm39) |
M136L |
probably benign |
Het |
| Gnas |
A |
G |
2: 174,141,277 (GRCm39) |
E482G |
unknown |
Het |
| Gpa33 |
T |
C |
1: 165,980,351 (GRCm39) |
L138P |
probably damaging |
Het |
| Hlf |
T |
C |
11: 90,236,714 (GRCm39) |
D181G |
probably damaging |
Het |
| Irgm1 |
A |
G |
11: 48,756,698 (GRCm39) |
L387S |
probably benign |
Het |
| Kctd1 |
T |
C |
18: 15,102,745 (GRCm39) |
E812G |
possibly damaging |
Het |
| Klra2 |
T |
C |
6: 131,205,214 (GRCm39) |
E209G |
probably benign |
Het |
| Klra3 |
C |
T |
6: 130,312,732 (GRCm39) |
V11M |
probably benign |
Het |
| Klrh1 |
G |
T |
6: 129,745,084 (GRCm39) |
H171N |
probably benign |
Het |
| Kmt2c |
T |
C |
5: 25,503,885 (GRCm39) |
S3808G |
probably benign |
Het |
| Krtap24-1 |
A |
C |
16: 88,408,888 (GRCm39) |
S79R |
probably benign |
Het |
| Limch1 |
T |
A |
5: 67,190,475 (GRCm39) |
H759Q |
probably benign |
Het |
| Map3k4 |
A |
G |
17: 12,490,433 (GRCm39) |
Y333H |
probably benign |
Het |
| Mmel1 |
A |
G |
4: 154,974,091 (GRCm39) |
Y377C |
probably damaging |
Het |
| Ms4a14 |
A |
T |
19: 11,281,113 (GRCm39) |
Y482N |
possibly damaging |
Het |
| Myo9b |
A |
G |
8: 71,801,675 (GRCm39) |
S1277G |
probably benign |
Het |
| Nab1 |
T |
C |
1: 52,529,667 (GRCm39) |
T77A |
possibly damaging |
Het |
| Obsl1 |
T |
C |
1: 75,482,841 (GRCm39) |
S10G |
probably benign |
Het |
| Odc1 |
A |
G |
12: 17,598,329 (GRCm39) |
T157A |
possibly damaging |
Het |
| Or2a5 |
T |
G |
6: 42,873,964 (GRCm39) |
L193R |
probably damaging |
Het |
| Or8b52 |
T |
C |
9: 38,576,780 (GRCm39) |
D120G |
probably damaging |
Het |
| Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
| Plpp1 |
T |
A |
13: 112,943,057 (GRCm39) |
|
probably benign |
Het |
| Prdm13 |
G |
A |
4: 21,679,125 (GRCm39) |
A455V |
possibly damaging |
Het |
| Ptpn13 |
A |
T |
5: 103,739,101 (GRCm39) |
Y2289F |
probably damaging |
Het |
| Ptpn18 |
G |
T |
1: 34,498,966 (GRCm39) |
R21L |
probably benign |
Het |
| Ptprd |
A |
G |
4: 75,916,736 (GRCm39) |
|
probably null |
Het |
| Rcn3 |
G |
T |
7: 44,733,095 (GRCm39) |
D258E |
probably damaging |
Het |
| Ro60 |
C |
T |
1: 143,641,170 (GRCm39) |
|
probably null |
Het |
| Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
| Sacs |
T |
A |
14: 61,429,895 (GRCm39) |
H651Q |
probably benign |
Het |
| Sacs |
T |
C |
14: 61,448,702 (GRCm39) |
S3583P |
probably damaging |
Het |
| Scel |
A |
G |
14: 103,829,807 (GRCm39) |
N463S |
possibly damaging |
Het |
| Serpinb2 |
A |
T |
1: 107,443,284 (GRCm39) |
I28F |
possibly damaging |
Het |
| Sin3b |
A |
G |
8: 73,473,131 (GRCm39) |
K484E |
probably benign |
Het |
| Snrnp48 |
T |
A |
13: 38,400,397 (GRCm39) |
V168D |
probably damaging |
Het |
| Snx18 |
T |
G |
13: 113,754,931 (GRCm39) |
M1L |
probably benign |
Het |
| Spata31h1 |
T |
C |
10: 82,131,295 (GRCm39) |
N572D |
probably benign |
Het |
| Srcap |
T |
A |
7: 127,158,204 (GRCm39) |
N2693K |
unknown |
Het |
| Stim1 |
A |
G |
7: 102,078,014 (GRCm39) |
D172G |
|
Het |
| Stip1 |
A |
T |
19: 7,002,687 (GRCm39) |
L414H |
probably damaging |
Het |
| Sun1 |
A |
G |
5: 139,209,390 (GRCm39) |
H40R |
probably damaging |
Het |
| Sva |
T |
A |
6: 42,019,182 (GRCm39) |
D117E |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 75,943,444 (GRCm39) |
D321G |
probably damaging |
Het |
| Trim45 |
A |
G |
3: 100,835,394 (GRCm39) |
D459G |
probably damaging |
Het |
| Ttc6 |
G |
A |
12: 57,697,790 (GRCm39) |
W43* |
probably null |
Het |
| Ugt2b35 |
A |
G |
5: 87,152,780 (GRCm39) |
T317A |
possibly damaging |
Het |
| Vmn2r53 |
G |
T |
7: 12,334,752 (GRCm39) |
Q303K |
probably benign |
Het |
| Yeats2 |
T |
C |
16: 19,969,312 (GRCm39) |
|
probably null |
Het |
| Zfp804a |
A |
G |
2: 82,088,747 (GRCm39) |
N859D |
probably benign |
Het |
| Zscan10 |
A |
T |
17: 23,824,580 (GRCm39) |
Q12L |
possibly 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 |
|
R4909:Usp32
|
UTSW |
11 |
84,946,598 (GRCm39) |
nonsense |
probably null |
|
|
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 |
|
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'- GCTTACCCACCAAAAGGCAT -3'
(R):5'- TTATCTGTGATTGAATTGTGGAACATG -3'
Sequencing Primer
(F):5'- TTGCCCAGCTAAGTAGGT -3'
(R):5'- GAATTGTGGAACATGCTCATTCC -3'
|
| Posted On |
2021-08-02 |
Incidental Mutation