Incidental Mutation 'R8924:Usp32'
| ID |
679483 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp32
|
| Ensembl Gene |
ENSMUSG00000000804 |
| Gene Name |
ubiquitin specific peptidase 32 |
| Synonyms |
6430526O11Rik, 2900074J03Rik |
| 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 |
84984442-85140161 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
C to T
at 85025544 bp (GRCm38)
|
| 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: 109,947,177 (GRCm38) |
V1145A |
probably benign |
Het |
| Ank1 |
T |
C |
8: 23,098,995 (GRCm38) |
M562T |
probably benign |
Het |
| Atn1 |
A |
T |
6: 124,745,248 (GRCm38) |
S881T |
probably benign |
Het |
| B3galt1 |
C |
T |
2: 68,118,715 (GRCm38) |
T258I |
probably benign |
Het |
| Bahcc1 |
C |
T |
11: 120,276,765 (GRCm38) |
L1331F |
probably benign |
Het |
| Capn12 |
G |
A |
7: 28,883,203 (GRCm38) |
V168M |
probably damaging |
Het |
| Card14 |
T |
C |
11: 119,326,104 (GRCm38) |
V338A |
possibly damaging |
Het |
| Cd27 |
T |
C |
6: 125,236,469 (GRCm38) |
|
probably benign |
Het |
| Cd37 |
A |
G |
7: 45,238,685 (GRCm38) |
L37P |
probably damaging |
Het |
| Cd96 |
A |
G |
16: 46,099,022 (GRCm38) |
L212P |
probably damaging |
Het |
| Celsr1 |
T |
C |
15: 86,032,470 (GRCm38) |
E434G |
possibly damaging |
Het |
| Cep152 |
A |
G |
2: 125,602,858 (GRCm38) |
M456T |
possibly damaging |
Het |
| Ces3b |
G |
A |
8: 105,084,987 (GRCm38) |
R45H |
probably benign |
Het |
| Cfap54 |
T |
G |
10: 93,001,823 (GRCm38) |
T1072P |
probably damaging |
Het |
| Chodl |
A |
T |
16: 78,941,771 (GRCm38) |
M172L |
possibly damaging |
Het |
| Cilp2 |
A |
G |
8: 69,886,458 (GRCm38) |
S47P |
probably damaging |
Het |
| Clasrp |
T |
C |
7: 19,584,307 (GRCm38) |
I596V |
unknown |
Het |
| Clcn2 |
C |
T |
16: 20,712,180 (GRCm38) |
V267I |
probably damaging |
Het |
| Cntln |
T |
A |
4: 84,888,699 (GRCm38) |
D139E |
probably damaging |
Het |
| Cyp2j12 |
A |
C |
4: 96,106,448 (GRCm38) |
N379K |
probably damaging |
Het |
| Defb21 |
T |
C |
2: 152,574,784 (GRCm38) |
V60A |
possibly damaging |
Het |
| Dnajc16 |
G |
T |
4: 141,766,707 (GRCm38) |
S543* |
probably null |
Het |
| Efcab12 |
G |
T |
6: 115,823,703 (GRCm38) |
H120N |
probably benign |
Het |
| Efl1 |
G |
A |
7: 82,762,953 (GRCm38) |
G850D |
probably benign |
Het |
| Efna1 |
T |
C |
3: 89,276,328 (GRCm38) |
M64V |
probably benign |
Het |
| Eif2ak3 |
T |
C |
6: 70,893,019 (GRCm38) |
W897R |
probably damaging |
Het |
| Eif2ak4 |
T |
A |
2: 118,428,032 (GRCm38) |
F621Y |
probably damaging |
Het |
| Erbin |
C |
A |
13: 103,839,458 (GRCm38) |
E643* |
probably null |
Het |
| Esr1 |
G |
A |
10: 4,857,176 (GRCm38) |
W364* |
probably null |
Het |
| Fam171a2 |
T |
C |
11: 102,440,035 (GRCm38) |
E206G |
possibly damaging |
Het |
| Fam90a1a |
T |
C |
8: 21,961,413 (GRCm38) |
F97L |
probably benign |
Het |
| Fap |
A |
T |
2: 62,547,821 (GRCm38) |
F181I |
probably benign |
Het |
| Fem1b |
T |
C |
9: 62,797,634 (GRCm38) |
N115D |
probably damaging |
Het |
| Gal3st2b |
G |
T |
1: 93,940,931 (GRCm38) |
A295S |
probably benign |
Het |
| Galnt10 |
G |
A |
11: 57,783,855 (GRCm38) |
|
probably benign |
Het |
| Gcfc2 |
T |
C |
6: 81,932,898 (GRCm38) |
V224A |
probably damaging |
Het |
| Gh |
T |
C |
11: 106,300,808 (GRCm38) |
E136G |
probably damaging |
Het |
| Gjd3 |
C |
T |
11: 98,982,499 (GRCm38) |
C173Y |
probably damaging |
Het |
| Gm11639 |
AACTCTA |
AA |
11: 104,915,427 (GRCm38) |
|
probably null |
Het |
| Gm12695 |
T |
A |
4: 96,762,809 (GRCm38) |
M136L |
probably benign |
Het |
| Gnas |
A |
G |
2: 174,299,484 (GRCm38) |
E482G |
unknown |
Het |
| Gpa33 |
T |
C |
1: 166,152,782 (GRCm38) |
L138P |
probably damaging |
Het |
| Hlf |
T |
C |
11: 90,345,888 (GRCm38) |
D181G |
probably damaging |
Het |
| Irgm1 |
A |
G |
11: 48,865,871 (GRCm38) |
L387S |
probably benign |
Het |
| Kctd1 |
T |
C |
18: 14,969,688 (GRCm38) |
E812G |
possibly damaging |
Het |
| Klra2 |
T |
C |
6: 131,228,251 (GRCm38) |
E209G |
probably benign |
Het |
| Klra3 |
C |
T |
6: 130,335,769 (GRCm38) |
V11M |
probably benign |
Het |
| Klrh1 |
G |
T |
6: 129,768,121 (GRCm38) |
H171N |
probably benign |
Het |
| Kmt2c |
T |
C |
5: 25,298,887 (GRCm38) |
S3808G |
probably benign |
Het |
| Krtap24-1 |
A |
C |
16: 88,612,000 (GRCm38) |
S79R |
probably benign |
Het |
| Limch1 |
T |
A |
5: 67,033,132 (GRCm38) |
H759Q |
probably benign |
Het |
| Map3k4 |
A |
G |
17: 12,271,546 (GRCm38) |
Y333H |
probably benign |
Het |
| Mmel1 |
A |
G |
4: 154,889,634 (GRCm38) |
Y377C |
probably damaging |
Het |
| Ms4a14 |
A |
T |
19: 11,303,749 (GRCm38) |
Y482N |
possibly damaging |
Het |
| Myo9b |
A |
G |
8: 71,349,031 (GRCm38) |
S1277G |
probably benign |
Het |
| Nab1 |
T |
C |
1: 52,490,508 (GRCm38) |
T77A |
possibly damaging |
Het |
| Obsl1 |
T |
C |
1: 75,506,197 (GRCm38) |
S10G |
probably benign |
Het |
| Odc1 |
A |
G |
12: 17,548,328 (GRCm38) |
T157A |
possibly damaging |
Het |
| Or2a5 |
T |
G |
6: 42,897,030 (GRCm38) |
L193R |
probably damaging |
Het |
| Or8b52 |
T |
C |
9: 38,665,484 (GRCm38) |
D120G |
probably damaging |
Het |
| Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm38) |
|
probably benign |
Het |
| Plpp1 |
T |
A |
13: 112,806,523 (GRCm38) |
|
probably benign |
Het |
| Prdm13 |
G |
A |
4: 21,679,125 (GRCm38) |
A455V |
possibly damaging |
Het |
| Ptpn13 |
A |
T |
5: 103,591,235 (GRCm38) |
Y2289F |
probably damaging |
Het |
| Ptpn18 |
G |
T |
1: 34,459,885 (GRCm38) |
R21L |
probably benign |
Het |
| Ptprd |
A |
G |
4: 75,998,499 (GRCm38) |
|
probably null |
Het |
| Rcn3 |
G |
T |
7: 45,083,671 (GRCm38) |
D258E |
probably damaging |
Het |
| Ro60 |
C |
T |
1: 143,765,432 (GRCm38) |
|
probably null |
Het |
| Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,579,907 (GRCm38) |
|
probably benign |
Het |
| Sacs |
T |
A |
14: 61,192,446 (GRCm38) |
H651Q |
probably benign |
Het |
| Sacs |
T |
C |
14: 61,211,253 (GRCm38) |
S3583P |
probably damaging |
Het |
| Scel |
A |
G |
14: 103,592,371 (GRCm38) |
N463S |
possibly damaging |
Het |
| Serpinb2 |
A |
T |
1: 107,515,554 (GRCm38) |
I28F |
possibly damaging |
Het |
| Sin3b |
A |
G |
8: 72,746,503 (GRCm38) |
K484E |
probably benign |
Het |
| Snrnp48 |
T |
A |
13: 38,216,421 (GRCm38) |
V168D |
probably damaging |
Het |
| Snx18 |
T |
G |
13: 113,618,395 (GRCm38) |
M1L |
probably benign |
Het |
| Spata31h1 |
T |
C |
10: 82,295,461 (GRCm38) |
N572D |
probably benign |
Het |
| Srcap |
T |
A |
7: 127,559,032 (GRCm38) |
N2693K |
unknown |
Het |
| Stim1 |
A |
G |
7: 102,428,807 (GRCm38) |
D172G |
|
Het |
| Stip1 |
A |
T |
19: 7,025,319 (GRCm38) |
L414H |
probably damaging |
Het |
| Sun1 |
A |
G |
5: 139,223,635 (GRCm38) |
H40R |
probably damaging |
Het |
| Sva |
T |
A |
6: 42,042,248 (GRCm38) |
D117E |
possibly damaging |
Het |
| Syne2 |
A |
G |
12: 75,896,670 (GRCm38) |
D321G |
probably damaging |
Het |
| Trim45 |
A |
G |
3: 100,928,078 (GRCm38) |
D459G |
probably damaging |
Het |
| Ttc6 |
G |
A |
12: 57,651,004 (GRCm38) |
W43* |
probably null |
Het |
| Ugt2b35 |
A |
G |
5: 87,004,921 (GRCm38) |
T317A |
possibly damaging |
Het |
| Vmn2r53 |
G |
T |
7: 12,600,825 (GRCm38) |
Q303K |
probably benign |
Het |
| Yeats2 |
T |
C |
16: 20,150,562 (GRCm38) |
|
probably null |
Het |
| Zfp804a |
A |
G |
2: 82,258,403 (GRCm38) |
N859D |
probably benign |
Het |
| Zscan10 |
A |
T |
17: 23,605,606 (GRCm38) |
Q12L |
possibly damaging |
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 |
|
R1712:Usp32
|
UTSW |
11 |
85,042,580 (GRCm38) |
missense |
probably benign |
0.12 |
|
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 |
|
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'- GCTTACCCACCAAAAGGCAT -3'
(R):5'- TTATCTGTGATTGAATTGTGGAACATG -3'
Sequencing Primer
(F):5'- TTGCCCAGCTAAGTAGGT -3'
(R):5'- GAATTGTGGAACATGCTCATTCC -3'
|
| Posted On |
2021-08-02 |
Incidental Mutation