Incidental Mutation 'R3162:Usp32'
| ID |
271691 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp32
|
| Ensembl Gene |
ENSMUSG00000000804 |
| Gene Name |
ubiquitin specific peptidase 32 |
| Synonyms |
6430526O11Rik, 2900074J03Rik |
| MMRRC Submission |
040613-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R3162 (G1)
|
| Quality Score |
225 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
84984442-85140161 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
A to G
at 85025536 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Tryptophan to Arginine
at position 861
(W861R)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000103710
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108075]
|
| AlphaFold |
F8VPZ3 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000000821
AA Change: W159R
|
| SMART Domains |
Protein: ENSMUSP00000000821
Gene: ENSMUSG00000000804
AA Change: W159R
| 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: W861R
PolyPhen 2
Score 0.974 (Sensitivity: 0.76; Specificity: 0.96)
|
| SMART Domains |
Protein: ENSMUSP00000103710
Gene: ENSMUSG00000000804
AA Change: W861R
| 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 |
|
| Meta Mutation Damage Score |
0.1212 |
| Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.0%
|
| Validation Efficiency |
98% (49/50) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 89 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 0610040J01Rik |
T |
C |
5: 63,896,490 (GRCm38) |
|
probably benign |
Het |
| 1700074P13Rik |
A |
G |
6: 40,926,069 (GRCm38) |
M123T |
probably benign |
Het |
| 4933412E24Rik |
T |
A |
15: 60,016,285 (GRCm38) |
E102V |
probably damaging |
Het |
| Adcy9 |
A |
G |
16: 4,311,588 (GRCm38) |
L715P |
probably damaging |
Het |
| Adgre4 |
T |
C |
17: 55,802,218 (GRCm38) |
|
probably benign |
Het |
| Amer2 |
A |
G |
14: 60,378,551 (GRCm38) |
D65G |
probably damaging |
Het |
| Atad2b |
C |
A |
12: 4,939,689 (GRCm38) |
N133K |
possibly damaging |
Het |
| AW551984 |
C |
A |
9: 39,593,029 (GRCm38) |
R547L |
probably damaging |
Het |
| B3galt6 |
A |
G |
4: 155,992,007 (GRCm38) |
Y204H |
probably benign |
Het |
| Btnl2 |
T |
C |
17: 34,358,065 (GRCm38) |
W65R |
probably damaging |
Het |
| Camk1g |
T |
C |
1: 193,359,807 (GRCm38) |
T45A |
possibly damaging |
Het |
| Caps2 |
C |
A |
10: 112,182,486 (GRCm38) |
Y180* |
probably null |
Het |
| Ccdc181 |
T |
A |
1: 164,280,296 (GRCm38) |
S183T |
probably damaging |
Het |
| Cdc14b |
A |
G |
13: 64,246,608 (GRCm38) |
|
probably benign |
Het |
| Cep350 |
T |
C |
1: 155,863,164 (GRCm38) |
H2311R |
probably benign |
Het |
| Cfap54 |
T |
A |
10: 93,045,278 (GRCm38) |
K349N |
probably damaging |
Het |
| Copa |
T |
A |
1: 172,091,233 (GRCm38) |
C127S |
probably damaging |
Het |
| Crbn |
T |
C |
6: 106,790,866 (GRCm38) |
Q221R |
probably benign |
Het |
| Dapk2 |
T |
G |
9: 66,254,611 (GRCm38) |
V267G |
probably damaging |
Het |
| Ddb1 |
T |
C |
19: 10,625,971 (GRCm38) |
L881P |
probably damaging |
Het |
| Decr1 |
T |
A |
4: 15,930,972 (GRCm38) |
D120V |
probably damaging |
Het |
| Dennd1c |
C |
T |
17: 57,066,562 (GRCm38) |
G637D |
possibly damaging |
Het |
| Dhrs3 |
A |
G |
4: 144,919,446 (GRCm38) |
D108G |
possibly damaging |
Het |
| Disp1 |
T |
C |
1: 183,087,242 (GRCm38) |
K1205E |
probably benign |
Het |
| Dnajc13 |
G |
T |
9: 104,219,898 (GRCm38) |
N510K |
possibly damaging |
Het |
| Dusp6 |
T |
C |
10: 99,264,082 (GRCm38) |
Y131H |
probably damaging |
Het |
| Eif2b2 |
A |
T |
12: 85,219,661 (GRCm38) |
M34L |
probably benign |
Het |
| Epsti1 |
A |
T |
14: 77,974,513 (GRCm38) |
|
probably benign |
Het |
| Errfi1 |
G |
A |
4: 150,867,359 (GRCm38) |
E415K |
probably damaging |
Het |
| Ext1 |
T |
C |
15: 53,344,604 (GRCm38) |
N254D |
possibly damaging |
Het |
| Fam84b |
A |
T |
15: 60,823,447 (GRCm38) |
V150E |
probably damaging |
Het |
| Gm7337 |
A |
C |
5: 87,851,557 (GRCm38) |
|
noncoding transcript |
Het |
| Hnrnpu |
T |
C |
1: 178,331,125 (GRCm38) |
|
probably benign |
Het |
| Hyal3 |
T |
A |
9: 107,586,806 (GRCm38) |
C407S |
probably damaging |
Het |
| Insr |
T |
G |
8: 3,161,416 (GRCm38) |
N1141T |
possibly damaging |
Het |
| Ipo9 |
T |
C |
1: 135,409,476 (GRCm38) |
T174A |
probably benign |
Het |
| Iqgap1 |
G |
A |
7: 80,752,338 (GRCm38) |
A393V |
probably benign |
Het |
| Irak2 |
G |
T |
6: 113,672,760 (GRCm38) |
A119S |
probably benign |
Het |
| Itgb2l |
A |
G |
16: 96,437,389 (GRCm38) |
L70P |
probably damaging |
Het |
| Itsn1 |
C |
A |
16: 91,853,044 (GRCm38) |
S202* |
probably null |
Het |
| Ivd |
T |
C |
2: 118,862,169 (GRCm38) |
|
probably null |
Het |
| Leprot |
C |
T |
4: 101,657,893 (GRCm38) |
T89I |
probably damaging |
Het |
| Mill2 |
A |
C |
7: 18,856,174 (GRCm38) |
E127A |
probably benign |
Het |
| Msh6 |
T |
C |
17: 87,985,481 (GRCm38) |
Y555H |
probably damaging |
Het |
| Myo18b |
A |
C |
5: 112,692,728 (GRCm38) |
S2400A |
probably damaging |
Het |
| Naa25 |
A |
G |
5: 121,435,072 (GRCm38) |
|
probably null |
Het |
| Nop2 |
A |
G |
6: 125,134,592 (GRCm38) |
N96S |
probably benign |
Het |
| Nup155 |
G |
T |
15: 8,148,383 (GRCm38) |
R1083S |
possibly damaging |
Het |
| Nusap1 |
A |
T |
2: 119,630,404 (GRCm38) |
Q126L |
possibly damaging |
Het |
| Olfr1042 |
T |
C |
2: 86,160,095 (GRCm38) |
I92V |
probably benign |
Het |
| Olfr1263 |
T |
G |
2: 90,015,021 (GRCm38) |
Y30* |
probably null |
Het |
| Olfr1351 |
C |
A |
10: 79,017,604 (GRCm38) |
T94N |
probably benign |
Het |
| Olfr156 |
T |
A |
4: 43,820,544 (GRCm38) |
K272N |
probably benign |
Het |
| Olfr30 |
T |
C |
11: 58,455,227 (GRCm38) |
T241A |
probably damaging |
Het |
| Olfr739 |
T |
A |
14: 50,425,031 (GRCm38) |
C171S |
probably damaging |
Het |
| Olfr986 |
G |
T |
9: 40,187,605 (GRCm38) |
Q163H |
probably benign |
Het |
| Pde5a |
T |
A |
3: 122,781,628 (GRCm38) |
L356* |
probably null |
Het |
| Pdik1l |
A |
G |
4: 134,284,250 (GRCm38) |
L94S |
probably damaging |
Het |
| Pkdrej |
T |
A |
15: 85,816,617 (GRCm38) |
D1706V |
probably damaging |
Het |
| Pkhd1l1 |
A |
G |
15: 44,505,528 (GRCm38) |
I856M |
probably damaging |
Het |
| Prkcz |
A |
T |
4: 155,290,524 (GRCm38) |
D114E |
probably benign |
Het |
| Psap |
T |
C |
10: 60,277,753 (GRCm38) |
L4P |
possibly damaging |
Het |
| Ptprk |
T |
C |
10: 28,592,826 (GRCm38) |
V1402A |
probably benign |
Het |
| Rai14 |
T |
C |
15: 10,633,164 (GRCm38) |
T47A |
possibly damaging |
Het |
| Ralgapa1 |
A |
T |
12: 55,709,586 (GRCm38) |
N1075K |
probably damaging |
Het |
| Rlf |
A |
G |
4: 121,148,847 (GRCm38) |
S979P |
probably damaging |
Het |
| Rps2 |
G |
T |
17: 24,720,978 (GRCm38) |
A129S |
probably benign |
Het |
| Serinc2 |
A |
G |
4: 130,260,735 (GRCm38) |
S175P |
probably benign |
Het |
| Skiv2l |
C |
T |
17: 34,847,813 (GRCm38) |
W88* |
probably null |
Het |
| Socs5 |
A |
T |
17: 87,134,718 (GRCm38) |
Q362L |
probably damaging |
Het |
| Srbd1 |
A |
T |
17: 86,130,215 (GRCm38) |
D233E |
probably benign |
Het |
| Srgap3 |
A |
G |
6: 112,729,658 (GRCm38) |
V826A |
probably benign |
Het |
| Tacr2 |
A |
G |
10: 62,265,245 (GRCm38) |
D378G |
probably benign |
Het |
| Taok2 |
A |
G |
7: 126,875,175 (GRCm38) |
I294T |
possibly damaging |
Het |
| Tert |
A |
G |
13: 73,627,409 (GRCm38) |
E93G |
possibly damaging |
Het |
| Tns2 |
A |
G |
15: 102,113,336 (GRCm38) |
E1118G |
possibly damaging |
Het |
| Topaz1 |
T |
C |
9: 122,749,381 (GRCm38) |
I452T |
probably benign |
Het |
| Trak1 |
C |
T |
9: 121,451,734 (GRCm38) |
|
probably benign |
Het |
| Ttc22 |
A |
T |
4: 106,623,079 (GRCm38) |
I177F |
probably damaging |
Het |
| Tuba8 |
A |
G |
6: 121,222,738 (GRCm38) |
D127G |
possibly damaging |
Het |
| Tulp4 |
A |
G |
17: 6,198,708 (GRCm38) |
M1V |
probably null |
Het |
| Urb1 |
A |
G |
16: 90,797,903 (GRCm38) |
L247P |
probably damaging |
Het |
| Vmn1r48 |
G |
A |
6: 90,036,378 (GRCm38) |
T155I |
probably benign |
Het |
| Vmn2r117 |
A |
G |
17: 23,460,378 (GRCm38) |
L624P |
probably damaging |
Het |
| Vmn2r86 |
T |
C |
10: 130,455,804 (GRCm38) |
R31G |
probably damaging |
Het |
| Vstm5 |
T |
G |
9: 15,257,298 (GRCm38) |
S53A |
probably benign |
Het |
| Wnt5a |
T |
C |
14: 28,522,488 (GRCm38) |
Y231H |
probably benign |
Het |
| Yeats2 |
T |
C |
16: 20,193,645 (GRCm38) |
V531A |
probably damaging |
Het |
| Zw10 |
T |
C |
9: 49,077,560 (GRCm38) |
Y709H |
probably 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 |
|
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'- TGTACATATACACTGCCCAGC -3'
(R):5'- AATTGTGGAACATGCTCATTCC -3'
Sequencing Primer
(F):5'- TGTACATATACACTGCCCAGCTTACC -3'
(R):5'- CCCAAGAACTTCTGGCTT -3'
|
| Posted On |
2015-03-25 |
Incidental Mutation