Incidental Mutation 'R5213:Usp32'
| ID |
403283 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp32
|
| Ensembl Gene |
ENSMUSG00000000804 |
| Gene Name |
ubiquitin specific peptidase 32 |
| Synonyms |
6430526O11Rik, 2900074J03Rik |
| MMRRC Submission |
042854-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R5213 (G1)
|
| Quality Score |
225 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
84984442-85140161 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 85022259 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Asparagine to Isoleucine
at position 941
(N941I)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000103710
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000108075]
|
| AlphaFold |
F8VPZ3 |
| Predicted Effect |
unknown
Transcript: ENSMUST00000000821
AA Change: N239I
|
| SMART Domains |
Protein: ENSMUSP00000000821
Gene: ENSMUSG00000000804
AA Change: N239I
| 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: N941I
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000103710
Gene: ENSMUSG00000000804
AA Change: N941I
| 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: 99.3%
- 3x: 98.7%
- 10x: 97.3%
- 20x: 95.4%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 82 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 2810474O19Rik |
C |
A |
6: 149,326,053 (GRCm38) |
P199Q |
possibly damaging |
Het |
| 4430402I18Rik |
A |
T |
19: 28,963,564 (GRCm38) |
V50E |
probably benign |
Het |
| Adamtsl1 |
C |
A |
4: 86,385,628 (GRCm38) |
H1342N |
possibly damaging |
Het |
| Adcy2 |
G |
T |
13: 68,620,823 (GRCm38) |
T1062K |
possibly damaging |
Het |
| Aqr |
T |
C |
2: 114,113,327 (GRCm38) |
N1110S |
probably damaging |
Het |
| Atp10a |
C |
T |
7: 58,773,983 (GRCm38) |
T232I |
probably damaging |
Het |
| Atp5f1 |
T |
A |
3: 105,955,911 (GRCm38) |
K70* |
probably null |
Het |
| Atp8b4 |
A |
C |
2: 126,389,409 (GRCm38) |
|
probably null |
Het |
| Atraid |
A |
C |
5: 31,052,208 (GRCm38) |
Q72P |
probably damaging |
Het |
| Atxn2 |
G |
T |
5: 121,814,480 (GRCm38) |
|
probably null |
Het |
| Best3 |
A |
T |
10: 117,024,472 (GRCm38) |
T546S |
probably benign |
Het |
| Brd3 |
T |
C |
2: 27,463,948 (GRCm38) |
K51E |
possibly damaging |
Het |
| Brip1 |
A |
G |
11: 86,143,321 (GRCm38) |
S525P |
possibly damaging |
Het |
| Cenpf |
A |
G |
1: 189,654,980 (GRCm38) |
I1701T |
probably benign |
Het |
| Chrna9 |
A |
T |
5: 65,971,084 (GRCm38) |
K208* |
probably null |
Het |
| Clec2l |
T |
A |
6: 38,680,192 (GRCm38) |
C197S |
probably damaging |
Het |
| Crp |
A |
G |
1: 172,698,519 (GRCm38) |
H57R |
probably benign |
Het |
| Cyp27b1 |
C |
A |
10: 127,052,095 (GRCm38) |
T492N |
probably damaging |
Het |
| Dock4 |
A |
T |
12: 40,676,742 (GRCm38) |
I340F |
probably damaging |
Het |
| Dsg1b |
A |
T |
18: 20,395,930 (GRCm38) |
D241V |
probably damaging |
Het |
| Epg5 |
G |
T |
18: 78,014,834 (GRCm38) |
V1865L |
probably benign |
Het |
| Erap1 |
A |
G |
13: 74,671,495 (GRCm38) |
|
probably null |
Het |
| Fat2 |
C |
T |
11: 55,253,832 (GRCm38) |
C4072Y |
probably benign |
Het |
| Fat4 |
T |
A |
3: 38,980,191 (GRCm38) |
I2664N |
possibly damaging |
Het |
| Gabrp |
A |
G |
11: 33,567,211 (GRCm38) |
|
probably null |
Het |
| Glis2 |
G |
T |
16: 4,614,082 (GRCm38) |
|
probably benign |
Het |
| Gm11487 |
G |
T |
4: 73,401,334 (GRCm38) |
Q302K |
probably damaging |
Het |
| Gm17654 |
A |
G |
14: 43,579,102 (GRCm38) |
S15P |
probably damaging |
Het |
| Gm21836 |
A |
G |
9: 124,493,753 (GRCm38) |
V14A |
unknown |
Het |
| Gon7 |
G |
A |
12: 102,754,121 (GRCm38) |
T84I |
possibly damaging |
Het |
| Greb1 |
G |
T |
12: 16,714,790 (GRCm38) |
Y447* |
probably null |
Het |
| Grip2 |
A |
T |
6: 91,779,831 (GRCm38) |
D546E |
probably benign |
Het |
| Hectd1 |
A |
G |
12: 51,802,533 (GRCm38) |
|
probably null |
Het |
| Il1f6 |
T |
A |
2: 24,224,474 (GRCm38) |
F120L |
probably damaging |
Het |
| Itga4 |
T |
C |
2: 79,320,576 (GRCm38) |
V842A |
probably benign |
Het |
| Khsrp |
G |
A |
17: 57,024,366 (GRCm38) |
A404V |
probably benign |
Het |
| Map3k11 |
T |
C |
19: 5,690,641 (GRCm38) |
V132A |
probably damaging |
Het |
| Mcub |
A |
C |
3: 129,916,997 (GRCm38) |
F262C |
probably benign |
Het |
| Mysm1 |
A |
T |
4: 94,948,377 (GRCm38) |
V732E |
probably damaging |
Het |
| Npr2 |
T |
A |
4: 43,640,673 (GRCm38) |
|
probably null |
Het |
| Olfr101 |
T |
C |
17: 37,300,051 (GRCm38) |
I124V |
probably damaging |
Het |
| Olfr172 |
T |
C |
16: 58,760,621 (GRCm38) |
Y185C |
probably damaging |
Het |
| Olfr975 |
A |
C |
9: 39,950,093 (GRCm38) |
I226S |
probably damaging |
Het |
| Oxgr1 |
G |
T |
14: 120,022,140 (GRCm38) |
Y218* |
probably null |
Het |
| Paf1 |
A |
G |
7: 28,395,972 (GRCm38) |
Q161R |
possibly damaging |
Het |
| Pck1 |
A |
T |
2: 173,156,085 (GRCm38) |
K316* |
probably null |
Het |
| Plac8 |
T |
A |
5: 100,556,505 (GRCm38) |
M109L |
probably benign |
Het |
| Plagl2 |
A |
T |
2: 153,232,319 (GRCm38) |
C221S |
probably damaging |
Het |
| Polg |
T |
C |
7: 79,454,098 (GRCm38) |
D870G |
probably damaging |
Het |
| Polr2k |
T |
A |
15: 36,174,997 (GRCm38) |
M1K |
probably null |
Het |
| Prdm9 |
T |
C |
17: 15,555,154 (GRCm38) |
H276R |
probably damaging |
Het |
| Rgs12 |
T |
A |
5: 34,965,320 (GRCm38) |
I149N |
probably damaging |
Het |
| Serpina3i |
A |
G |
12: 104,265,655 (GRCm38) |
I184V |
probably benign |
Het |
| Shank3 |
A |
G |
15: 89,533,278 (GRCm38) |
E26G |
possibly damaging |
Het |
| Skil |
T |
C |
3: 31,117,451 (GRCm38) |
S575P |
probably damaging |
Het |
| Slc13a1 |
A |
G |
6: 24,108,159 (GRCm38) |
L306P |
probably damaging |
Het |
| Slc20a1 |
G |
T |
2: 129,200,509 (GRCm38) |
W166L |
probably damaging |
Het |
| Slc45a2 |
C |
T |
15: 11,027,785 (GRCm38) |
T480I |
probably damaging |
Het |
| Snrnp200 |
G |
T |
2: 127,231,741 (GRCm38) |
G1353V |
probably damaging |
Het |
| Sphkap |
A |
G |
1: 83,280,503 (GRCm38) |
I173T |
probably damaging |
Het |
| Stab2 |
A |
T |
10: 86,907,197 (GRCm38) |
F1183I |
probably damaging |
Het |
| Stard9 |
A |
G |
2: 120,699,226 (GRCm38) |
D1988G |
probably damaging |
Het |
| Tank |
T |
A |
2: 61,649,948 (GRCm38) |
I276N |
probably benign |
Het |
| Tcaf3 |
A |
G |
6: 42,591,467 (GRCm38) |
W652R |
probably damaging |
Het |
| Tgm2 |
G |
A |
2: 158,143,060 (GRCm38) |
T42I |
possibly damaging |
Het |
| Tnni2 |
G |
T |
7: 142,443,302 (GRCm38) |
|
probably null |
Het |
| Tns1 |
A |
G |
1: 73,953,612 (GRCm38) |
S9P |
probably damaging |
Het |
| Tram1 |
T |
C |
1: 13,579,742 (GRCm38) |
Y86C |
probably damaging |
Het |
| Trdv2-1 |
T |
C |
14: 53,946,406 (GRCm38) |
S32P |
probably benign |
Het |
| Trim24 |
T |
C |
6: 37,957,075 (GRCm38) |
I651T |
probably damaging |
Het |
| Trpm3 |
T |
G |
19: 22,697,454 (GRCm38) |
Y72* |
probably null |
Het |
| Ube2o |
G |
A |
11: 116,541,459 (GRCm38) |
P894S |
possibly damaging |
Het |
| Ubr4 |
C |
T |
4: 139,402,566 (GRCm38) |
R666* |
probably null |
Het |
| Ugt1a8 |
T |
A |
1: 88,088,123 (GRCm38) |
L86* |
probably null |
Het |
| Utrn |
C |
T |
10: 12,636,760 (GRCm38) |
V2322M |
probably damaging |
Het |
| Vmn1r184 |
A |
T |
7: 26,267,711 (GRCm38) |
Y294F |
probably damaging |
Het |
| Vmn2r108 |
T |
C |
17: 20,471,493 (GRCm38) |
N256S |
probably benign |
Het |
| Wdr7 |
T |
C |
18: 63,755,126 (GRCm38) |
S557P |
probably damaging |
Het |
| Xrra1 |
C |
A |
7: 99,898,483 (GRCm38) |
P293Q |
possibly damaging |
Het |
| Zc3h18 |
A |
G |
8: 122,383,649 (GRCm38) |
D79G |
probably damaging |
Het |
| Zfp74 |
A |
T |
7: 29,935,243 (GRCm38) |
Y347N |
probably damaging |
Het |
| Zfp740 |
T |
C |
15: 102,212,647 (GRCm38) |
C169R |
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 |
|
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'- TCTTTTCTGGTAGACAACATTTTCA -3'
(R):5'- CCAATCAGAAGTCTTTATCAGATAGAC -3'
Sequencing Primer
(F):5'- GAAGTACATAGTGAGCCTCTGACTC -3'
(R):5'- GCTATTTGCAAGTCAGGTA -3'
|
| Posted On |
2016-07-22 |
Incidental Mutation