Incidental Mutation 'R7502:Usp32'
| ID |
581571 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp32
|
| Ensembl Gene |
ENSMUSG00000000804 |
| Gene Name |
ubiquitin specific peptidase 32 |
| Synonyms |
6430526O11Rik, 2900074J03Rik |
| MMRRC Submission |
045575-MU
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R7502 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
11 |
| Chromosomal Location |
84984442-85140161 bp(-) (GRCm38) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 85022898 bp (GRCm38)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Aspartic acid to Glycine
at position 869
(D869G)
|
| 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: D167G
| 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 |
possibly damaging
Transcript: ENSMUST00000108075
AA Change: D869G
PolyPhen 2
Score 0.484 (Sensitivity: 0.89; Specificity: 0.90)
|
| SMART Domains |
Protein: ENSMUSP00000103710
Gene: ENSMUSG00000000804
AA Change: D869G
| 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: 100.0%
- 10x: 99.7%
- 20x: 99.1%
|
| Validation Efficiency |
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 87 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 1110008L16Rik |
T |
C |
12: 55,304,421 (GRCm38) |
Y172H |
probably damaging |
Het |
| Acan |
A |
G |
7: 79,094,203 (GRCm38) |
T661A |
probably damaging |
Het |
| Actrt2 |
T |
C |
4: 154,666,926 (GRCm38) |
Y251C |
probably benign |
Het |
| Adat3 |
T |
A |
10: 80,606,421 (GRCm38) |
V31D |
probably damaging |
Het |
| Adgrf4 |
T |
C |
17: 42,669,657 (GRCm38) |
H179R |
possibly damaging |
Het |
| Ahcyl1 |
A |
T |
3: 107,671,197 (GRCm38) |
Y241* |
probably null |
Het |
| Anks1 |
C |
A |
17: 28,008,140 (GRCm38) |
T589K |
possibly damaging |
Het |
| Arhgap15 |
A |
G |
2: 43,780,618 (GRCm38) |
T5A |
probably benign |
Het |
| Cacna1e |
A |
T |
1: 154,468,988 (GRCm38) |
M1130K |
probably null |
Het |
| Ccdc121 |
G |
A |
1: 181,510,878 (GRCm38) |
Q170* |
probably null |
Het |
| Ccdc173 |
A |
T |
2: 69,776,144 (GRCm38) |
D309E |
probably benign |
Het |
| Ceacam18 |
A |
T |
7: 43,636,874 (GRCm38) |
D57V |
probably damaging |
Het |
| Celf1 |
C |
T |
2: 91,004,755 (GRCm38) |
Q194* |
probably null |
Het |
| Celsr2 |
T |
A |
3: 108,398,902 (GRCm38) |
T2029S |
probably benign |
Het |
| Cep170 |
T |
C |
1: 176,756,029 (GRCm38) |
D163G |
probably damaging |
Het |
| Cftr |
T |
C |
6: 18,214,296 (GRCm38) |
F157S |
probably damaging |
Het |
| Chchd3 |
T |
C |
6: 32,968,229 (GRCm38) |
E114G |
probably damaging |
Het |
| Cntnap2 |
T |
A |
6: 46,484,029 (GRCm38) |
S666R |
possibly damaging |
Het |
| Col6a5 |
C |
T |
9: 105,875,876 (GRCm38) |
V2266I |
probably benign |
Het |
| Ctr9 |
A |
G |
7: 111,033,926 (GRCm38) |
D127G |
probably benign |
Het |
| Ctsl |
A |
T |
13: 64,367,068 (GRCm38) |
F141I |
probably damaging |
Het |
| Dcpp1 |
T |
A |
17: 23,882,641 (GRCm38) |
Y121* |
probably null |
Het |
| Ddx42 |
T |
C |
11: 106,247,739 (GRCm38) |
V788A |
probably benign |
Het |
| Ehd4 |
T |
C |
2: 120,091,393 (GRCm38) |
I461V |
probably benign |
Het |
| Elp6 |
C |
A |
9: 110,305,308 (GRCm38) |
L5I |
possibly damaging |
Het |
| Faap20 |
T |
C |
4: 155,250,336 (GRCm38) |
S2P |
|
Het |
| Fam98b |
A |
C |
2: 117,263,863 (GRCm38) |
Y218S |
probably damaging |
Het |
| Fbxl4 |
T |
A |
4: 22,376,655 (GRCm38) |
D30E |
probably benign |
Het |
| Fcrlb |
T |
C |
1: 170,908,641 (GRCm38) |
T189A |
probably damaging |
Het |
| Gfpt1 |
A |
G |
6: 87,066,689 (GRCm38) |
D302G |
probably benign |
Het |
| Gzmg |
T |
G |
14: 56,156,827 (GRCm38) |
E203D |
not run |
Het |
| Hrasls |
T |
C |
16: 29,228,167 (GRCm38) |
V146A |
probably benign |
Het |
| Hsph1 |
A |
C |
5: 149,630,373 (GRCm38) |
V210G |
probably damaging |
Het |
| Il20rb |
A |
T |
9: 100,468,426 (GRCm38) |
M138K |
probably damaging |
Het |
| Itpr1 |
A |
T |
6: 108,383,678 (GRCm38) |
E688D |
probably benign |
Het |
| Jmjd1c |
T |
G |
10: 67,232,015 (GRCm38) |
S1585A |
probably damaging |
Het |
| Kcnk3 |
A |
T |
5: 30,622,718 (GRCm38) |
T371S |
possibly damaging |
Het |
| Kif11 |
T |
A |
19: 37,409,807 (GRCm38) |
S694T |
possibly damaging |
Het |
| Kpna7 |
T |
A |
5: 145,005,921 (GRCm38) |
H85L |
probably benign |
Het |
| Lipf |
A |
T |
19: 33,976,606 (GRCm38) |
I366F |
probably damaging |
Het |
| Lrrc27 |
A |
G |
7: 139,214,832 (GRCm38) |
H37R |
probably benign |
Het |
| Mfsd7a |
G |
A |
5: 108,443,780 (GRCm38) |
|
probably null |
Het |
| Mki67 |
T |
C |
7: 135,700,783 (GRCm38) |
T841A |
possibly damaging |
Het |
| Mtss1 |
A |
G |
15: 58,948,361 (GRCm38) |
S120P |
probably damaging |
Het |
| Nav1 |
A |
G |
1: 135,469,666 (GRCm38) |
W922R |
probably damaging |
Het |
| Nwd1 |
A |
G |
8: 72,707,393 (GRCm38) |
E1206G |
probably damaging |
Het |
| Obscn |
T |
C |
11: 58,994,809 (GRCm38) |
S7933G |
unknown |
Het |
| Olfr117 |
T |
A |
17: 37,660,231 (GRCm38) |
Y34F |
probably damaging |
Het |
| Olfr1263 |
T |
C |
2: 90,015,011 (GRCm38) |
L27S |
probably benign |
Het |
| Olfr267 |
T |
C |
4: 58,785,648 (GRCm38) |
I25V |
probably benign |
Het |
| Olfr409-ps1 |
T |
C |
11: 74,317,184 (GRCm38) |
V53A |
probably benign |
Het |
| Olfr71 |
T |
C |
4: 43,706,316 (GRCm38) |
H84R |
probably damaging |
Het |
| Otog |
A |
T |
7: 46,298,615 (GRCm38) |
I162F |
probably damaging |
Het |
| Paf1 |
G |
A |
7: 28,395,868 (GRCm38) |
V153I |
possibly damaging |
Het |
| Pcdhga11 |
T |
A |
18: 37,756,501 (GRCm38) |
D187E |
probably benign |
Het |
| Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm38) |
|
probably benign |
Het |
| Pitrm1 |
G |
T |
13: 6,560,622 (GRCm38) |
R424L |
probably damaging |
Het |
| Pla2g4e |
T |
A |
2: 120,174,338 (GRCm38) |
|
probably null |
Het |
| Prrc2a |
T |
C |
17: 35,162,310 (GRCm38) |
N61S |
unknown |
Het |
| Ror1 |
T |
A |
4: 100,333,630 (GRCm38) |
D61E |
probably benign |
Het |
| Ryr3 |
G |
A |
2: 112,712,361 (GRCm38) |
P3168S |
probably benign |
Het |
| Serinc4 |
T |
A |
2: 121,453,769 (GRCm38) |
I289F |
probably damaging |
Het |
| Sez6l |
A |
T |
5: 112,475,481 (GRCm38) |
L68H |
possibly damaging |
Het |
| Sez6l2 |
A |
G |
7: 126,961,743 (GRCm38) |
E460G |
probably benign |
Het |
| Sh3tc1 |
C |
T |
5: 35,706,062 (GRCm38) |
G927D |
probably damaging |
Het |
| Slc22a27 |
G |
C |
19: 7,926,382 (GRCm38) |
T130S |
probably damaging |
Het |
| Slc38a8 |
C |
A |
8: 119,501,081 (GRCm38) |
A37S |
possibly damaging |
Het |
| Slc40a1 |
T |
C |
1: 45,918,974 (GRCm38) |
N100D |
probably damaging |
Het |
| Snx30 |
T |
C |
4: 59,894,567 (GRCm38) |
F382L |
possibly damaging |
Het |
| Sox1 |
A |
G |
8: 12,396,913 (GRCm38) |
N185D |
possibly damaging |
Het |
| Spsb1 |
C |
T |
4: 149,906,928 (GRCm38) |
R61H |
possibly damaging |
Het |
| Sptbn2 |
T |
C |
19: 4,748,082 (GRCm38) |
V1945A |
probably benign |
Het |
| St18 |
T |
A |
1: 6,827,970 (GRCm38) |
N665K |
probably benign |
Het |
| Syne1 |
A |
G |
10: 5,333,446 (GRCm38) |
S1540P |
probably damaging |
Het |
| Syne2 |
G |
A |
12: 76,094,326 (GRCm38) |
V1331M |
probably damaging |
Het |
| Tfap2c |
T |
C |
2: 172,551,719 (GRCm38) |
S185P |
probably benign |
Het |
| Tnfsf8 |
T |
A |
4: 63,851,161 (GRCm38) |
D71V |
probably damaging |
Het |
| Tnn |
T |
C |
1: 160,110,359 (GRCm38) |
D1196G |
probably benign |
Het |
| Ttll8 |
A |
G |
15: 88,933,436 (GRCm38) |
|
probably null |
Het |
| Tubgcp3 |
A |
G |
8: 12,641,207 (GRCm38) |
F444L |
probably damaging |
Het |
| Txndc11 |
G |
A |
16: 11,087,878 (GRCm38) |
P596L |
probably benign |
Het |
| Ubr4 |
C |
T |
4: 139,412,672 (GRCm38) |
P1189S |
possibly damaging |
Het |
| Vmn1r202 |
G |
T |
13: 22,502,018 (GRCm38) |
N76K |
probably damaging |
Het |
| Wfdc6a |
C |
T |
2: 164,579,841 (GRCm38) |
M132I |
probably benign |
Het |
| Wnk2 |
A |
T |
13: 49,147,244 (GRCm38) |
|
probably null |
Het |
| Xbp1 |
A |
G |
11: 5,524,683 (GRCm38) |
|
probably null |
Het |
| Zfp551 |
A |
T |
7: 12,415,798 (GRCm38) |
Y561* |
probably null |
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 |
|
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'- TTTTCAGAACTCTGTGACCTACCTG -3'
(R):5'- CTTGATAGGCCTGGGACAAC -3'
Sequencing Primer
(F):5'- GTGACCTACCTGTTATTTCTAAATGC -3'
(R):5'- AGGAGAAATAGATCAATTGTTGTACC -3'
|
| Posted On |
2019-10-17 |
Incidental Mutation