Incidental Mutation 'R9211:Usp32'
| ID |
698886 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Usp32
|
| Ensembl Gene |
ENSMUSG00000000804 |
| Gene Name |
ubiquitin specific peptidase 32 |
| Synonyms |
2900074J03Rik, 6430526O11Rik |
| MMRRC Submission |
|
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
R9211 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Validated
|
| Chromosome |
11 |
| Chromosomal Location |
84875268-85030987 bp(-) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
G to T
at 84913559 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Threonine to Lysine
at position 924
(T924K)
|
| 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: T222K
| 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: T924K
PolyPhen 2
Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
|
| SMART Domains |
Protein: ENSMUSP00000103710
Gene: ENSMUSG00000000804
AA Change: T924K
| 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: 99.8%
- 20x: 99.2%
|
| Validation Efficiency |
99% (86/87) |
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 86 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| 3110009E18Rik |
G |
T |
1: 120,099,161 (GRCm39) |
D85Y |
possibly damaging |
Het |
| Accs |
T |
C |
2: 93,668,614 (GRCm39) |
R315G |
probably damaging |
Het |
| Adam3 |
A |
C |
8: 25,177,910 (GRCm39) |
W668G |
probably benign |
Het |
| Adgrb2 |
T |
A |
4: 129,886,199 (GRCm39) |
V113E |
probably benign |
Het |
| Anapc4 |
C |
T |
5: 53,007,994 (GRCm39) |
T391I |
possibly damaging |
Het |
| Angpt2 |
C |
T |
8: 18,748,078 (GRCm39) |
G394D |
probably benign |
Het |
| Ankrd31 |
C |
G |
13: 97,029,551 (GRCm39) |
L1662V |
possibly damaging |
Het |
| Ankrd36 |
A |
G |
11: 5,612,370 (GRCm39) |
D1234G |
possibly damaging |
Het |
| Ankrd6 |
C |
T |
4: 32,806,580 (GRCm39) |
V558M |
probably damaging |
Het |
| Ankrd61 |
T |
A |
5: 143,828,358 (GRCm39) |
M206L |
probably benign |
Het |
| Arhgap33 |
C |
T |
7: 30,223,023 (GRCm39) |
G970R |
possibly damaging |
Het |
| Atf7 |
A |
G |
15: 102,437,117 (GRCm39) |
V115A |
unknown |
Het |
| Atp2c2 |
A |
T |
8: 120,446,032 (GRCm39) |
R65S |
probably benign |
Het |
| Atp8b5 |
T |
A |
4: 43,367,960 (GRCm39) |
M861K |
probably damaging |
Het |
| Bmi1 |
T |
C |
2: 18,689,152 (GRCm39) |
S279P |
probably benign |
Het |
| Bptf |
T |
G |
11: 106,946,124 (GRCm39) |
S2372R |
probably damaging |
Het |
| Cacnb2 |
A |
T |
2: 14,879,308 (GRCm39) |
I15L |
unknown |
Het |
| Card11 |
A |
G |
5: 140,869,375 (GRCm39) |
M807T |
probably benign |
Het |
| Ccdc175 |
A |
T |
12: 72,153,458 (GRCm39) |
D704E |
probably damaging |
Het |
| Cd300ld |
T |
A |
11: 114,878,386 (GRCm39) |
Y42F |
probably damaging |
Het |
| Cdh1 |
A |
T |
8: 107,390,962 (GRCm39) |
T693S |
probably benign |
Het |
| Clca4b |
T |
C |
3: 144,638,214 (GRCm39) |
Y16C |
possibly damaging |
Het |
| Col4a4 |
A |
G |
1: 82,506,501 (GRCm39) |
I273T |
unknown |
Het |
| Coro2b |
C |
A |
9: 62,427,662 (GRCm39) |
V9L |
probably benign |
Het |
| Crnkl1 |
T |
C |
2: 145,774,773 (GRCm39) |
D55G |
probably damaging |
Het |
| Dcps |
T |
A |
9: 35,035,872 (GRCm39) |
N338I |
probably damaging |
Het |
| Dusp2 |
A |
T |
2: 127,179,311 (GRCm39) |
H222L |
probably benign |
Het |
| Dync1li1 |
C |
A |
9: 114,518,012 (GRCm39) |
Y21* |
probably null |
Het |
| Efhb |
T |
G |
17: 53,756,507 (GRCm39) |
Q381H |
probably damaging |
Het |
| Elac2 |
A |
T |
11: 64,869,864 (GRCm39) |
|
probably benign |
Het |
| Etaa1 |
A |
G |
11: 17,896,053 (GRCm39) |
V688A |
possibly damaging |
Het |
| Fam120c |
C |
T |
X: 150,127,495 (GRCm39) |
H84Y |
probably benign |
Het |
| Fbxl7 |
T |
A |
15: 26,789,616 (GRCm39) |
N37I |
probably damaging |
Het |
| Fndc3b |
A |
T |
3: 27,523,086 (GRCm39) |
W498R |
probably damaging |
Het |
| Galc |
G |
A |
12: 98,173,699 (GRCm39) |
A621V |
probably benign |
Het |
| Gch1 |
A |
T |
14: 47,426,519 (GRCm39) |
I69N |
probably damaging |
Het |
| Gdpd4 |
T |
C |
7: 97,615,466 (GRCm39) |
V97A |
possibly damaging |
Het |
| Hirip3 |
C |
T |
7: 126,463,567 (GRCm39) |
R485* |
probably null |
Het |
| Hmgcs2 |
C |
T |
3: 98,204,748 (GRCm39) |
T302I |
possibly damaging |
Het |
| Ing5 |
A |
T |
1: 93,740,409 (GRCm39) |
K137I |
possibly damaging |
Het |
| Kcnh8 |
T |
A |
17: 53,146,236 (GRCm39) |
Y375N |
probably damaging |
Het |
| Kdm3a |
C |
A |
6: 71,573,674 (GRCm39) |
W963L |
probably benign |
Het |
| Klra17 |
T |
G |
6: 129,842,651 (GRCm39) |
I216L |
possibly damaging |
Het |
| Kmt2e |
A |
G |
5: 23,669,770 (GRCm39) |
K86E |
possibly damaging |
Het |
| Krt42 |
T |
C |
11: 100,155,867 (GRCm39) |
N293S |
possibly damaging |
Het |
| Lrrc8d |
T |
A |
5: 105,960,216 (GRCm39) |
W209R |
probably damaging |
Het |
| Mettl23 |
C |
T |
11: 116,734,469 (GRCm39) |
P13S |
unknown |
Het |
| Ncln |
T |
C |
10: 81,323,527 (GRCm39) |
Y540C |
probably damaging |
Het |
| Neb |
C |
G |
2: 52,135,360 (GRCm39) |
G3250A |
probably damaging |
Het |
| Nebl |
A |
G |
2: 17,393,501 (GRCm39) |
|
probably null |
Het |
| Nqo2 |
A |
T |
13: 34,156,399 (GRCm39) |
T38S |
probably benign |
Het |
| Obscn |
A |
T |
11: 59,026,693 (GRCm39) |
I170N |
probably benign |
Het |
| Or2bd2 |
G |
T |
7: 6,443,417 (GRCm39) |
G173W |
probably damaging |
Het |
| Or4c100 |
A |
G |
2: 88,356,170 (GRCm39) |
D81G |
probably benign |
Het |
| Or5af2 |
A |
T |
11: 58,708,709 (GRCm39) |
N292Y |
probably damaging |
Het |
| Or5p6 |
C |
T |
7: 107,630,798 (GRCm39) |
V251I |
probably damaging |
Het |
| Or7g28 |
T |
A |
9: 19,271,824 (GRCm39) |
I276F |
possibly damaging |
Het |
| Or8k38 |
A |
T |
2: 86,488,024 (GRCm39) |
Y259* |
probably null |
Het |
| Pacs1 |
A |
T |
19: 5,189,057 (GRCm39) |
V775E |
probably damaging |
Het |
| Pheta2 |
A |
T |
15: 82,225,227 (GRCm39) |
|
probably benign |
Het |
| Pmfbp1 |
T |
C |
8: 110,262,445 (GRCm39) |
I713T |
probably benign |
Het |
| Pnma8b |
A |
G |
7: 16,679,589 (GRCm39) |
D191G |
unknown |
Het |
| Polr1a |
T |
C |
6: 71,943,521 (GRCm39) |
I1252T |
probably damaging |
Het |
| Prss16 |
A |
T |
13: 22,192,754 (GRCm39) |
M110K |
probably benign |
Het |
| Pygo2 |
T |
C |
3: 89,338,038 (GRCm39) |
|
probably null |
Het |
| Rab5b |
C |
A |
10: 128,519,063 (GRCm39) |
|
probably null |
Het |
| Reln |
G |
T |
5: 22,549,200 (GRCm39) |
Y69* |
probably null |
Het |
| Rgs12 |
T |
A |
5: 35,123,165 (GRCm39) |
M316K |
probably damaging |
Het |
| Rmi2 |
T |
C |
16: 10,657,743 (GRCm39) |
C118R |
possibly damaging |
Het |
| Rnf223 |
T |
A |
4: 156,216,834 (GRCm39) |
C70S |
probably damaging |
Het |
| Rxrb |
T |
A |
17: 34,255,626 (GRCm39) |
F371Y |
probably damaging |
Het |
| Smurf2 |
T |
A |
11: 106,759,463 (GRCm39) |
S78C |
probably damaging |
Het |
| Sorbs1 |
A |
T |
19: 40,332,798 (GRCm39) |
|
probably null |
Het |
| Spag17 |
C |
T |
3: 100,032,614 (GRCm39) |
|
probably benign |
Het |
| Spidr |
T |
C |
16: 15,871,319 (GRCm39) |
H217R |
probably benign |
Het |
| Tiam2 |
T |
G |
17: 3,498,729 (GRCm39) |
V835G |
possibly damaging |
Het |
| Tm2d2 |
C |
T |
8: 25,510,548 (GRCm39) |
R136* |
probably null |
Het |
| Tnks |
C |
T |
8: 35,316,489 (GRCm39) |
D877N |
probably damaging |
Het |
| Tns1 |
A |
G |
1: 73,956,948 (GRCm39) |
L491P |
possibly damaging |
Het |
| Trps1 |
A |
G |
15: 50,694,840 (GRCm39) |
I485T |
probably damaging |
Het |
| Tubgcp5 |
A |
G |
7: 55,456,331 (GRCm39) |
S308G |
probably benign |
Het |
| Ugt8a |
T |
C |
3: 125,661,130 (GRCm39) |
H454R |
probably damaging |
Het |
| Vmn2r91 |
A |
T |
17: 18,356,819 (GRCm39) |
K829* |
probably null |
Het |
| Zfc3h1 |
T |
C |
10: 115,248,328 (GRCm39) |
F1146L |
possibly damaging |
Het |
| Zfp729a |
G |
T |
13: 67,767,820 (GRCm39) |
A803E |
probably benign |
Het |
| Zfp990 |
A |
G |
4: 145,264,171 (GRCm39) |
T390A |
probably 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 |
|
R8924:Usp32
|
UTSW |
11 |
84,916,370 (GRCm39) |
missense |
probably damaging |
0.98 |
|
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 |
|
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'- TGAAGTTTCTTCCACGTCTGG -3'
(R):5'- TTCCTTGATAGGCCTGGGAC -3'
Sequencing Primer
(F):5'- TCCACGTCTGGAATTTAAGAAACGC -3'
(R):5'- GACAACCATCTAAGGAGAAATAGATC -3'
|
| Posted On |
2022-02-07 |
Incidental Mutation