Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam22 |
A |
G |
5: 8,167,583 (GRCm39) |
|
probably null |
Het |
Adamts9 |
A |
T |
6: 92,837,170 (GRCm39) |
S1164T |
probably benign |
Het |
Bcat1 |
A |
T |
6: 144,985,222 (GRCm39) |
I140N |
probably damaging |
Het |
Bod1l |
T |
C |
5: 41,957,129 (GRCm39) |
T2832A |
probably benign |
Het |
Brca2 |
A |
T |
5: 150,459,977 (GRCm39) |
E417D |
possibly damaging |
Het |
Ccdc88b |
T |
C |
19: 6,831,268 (GRCm39) |
D558G |
possibly damaging |
Het |
Ccdc88b |
T |
C |
19: 6,833,213 (GRCm39) |
E278G |
probably damaging |
Het |
Celsr1 |
G |
T |
15: 85,917,286 (GRCm39) |
S229* |
probably null |
Het |
Cenpf |
G |
T |
1: 189,388,987 (GRCm39) |
T1615K |
probably damaging |
Het |
Cep250 |
T |
C |
2: 155,830,354 (GRCm39) |
|
probably null |
Het |
Clec4d |
T |
C |
6: 123,251,757 (GRCm39) |
F213S |
probably damaging |
Het |
Clip4 |
G |
A |
17: 72,117,884 (GRCm39) |
G310R |
probably damaging |
Het |
Csmd1 |
G |
A |
8: 15,962,430 (GRCm39) |
R3255W |
probably damaging |
Het |
Ctsm |
T |
C |
13: 61,687,612 (GRCm39) |
D82G |
probably damaging |
Het |
Cyp26a1 |
A |
G |
19: 37,686,790 (GRCm39) |
T81A |
probably damaging |
Het |
Dld |
A |
G |
12: 31,390,885 (GRCm39) |
V187A |
probably benign |
Het |
Dmrt2 |
T |
A |
19: 25,655,477 (GRCm39) |
Y359N |
probably benign |
Het |
Dnah9 |
T |
C |
11: 65,846,570 (GRCm39) |
N2914S |
probably benign |
Het |
Dpyd |
A |
T |
3: 118,553,303 (GRCm39) |
|
probably null |
Het |
Fgl2 |
A |
C |
5: 21,577,920 (GRCm39) |
Q69P |
probably damaging |
Het |
Gadd45gip1 |
A |
T |
8: 85,560,780 (GRCm39) |
I132F |
probably damaging |
Het |
Gm15446 |
T |
C |
5: 110,090,743 (GRCm39) |
C332R |
probably damaging |
Het |
Gm15737 |
A |
T |
6: 92,856,640 (GRCm39) |
E23V |
unknown |
Het |
Gm5111 |
A |
G |
6: 48,567,037 (GRCm39) |
H84R |
unknown |
Het |
Golga3 |
G |
A |
5: 110,355,619 (GRCm39) |
S991N |
probably benign |
Het |
H2-M10.3 |
A |
G |
17: 36,678,919 (GRCm39) |
Y50H |
probably damaging |
Het |
Hivep2 |
C |
T |
10: 14,005,621 (GRCm39) |
H740Y |
probably benign |
Het |
Il18rap |
C |
T |
1: 40,582,177 (GRCm39) |
T366M |
probably benign |
Het |
Ints7 |
T |
A |
1: 191,351,872 (GRCm39) |
S860R |
probably benign |
Het |
Lipi |
T |
A |
16: 75,362,461 (GRCm39) |
T217S |
possibly damaging |
Het |
Lrrc2 |
G |
T |
9: 110,791,722 (GRCm39) |
C158F |
probably benign |
Het |
Lrrc30 |
T |
C |
17: 67,938,854 (GRCm39) |
D242G |
probably benign |
Het |
Map1a |
A |
T |
2: 121,133,854 (GRCm39) |
M1557L |
probably benign |
Het |
Matn2 |
A |
G |
15: 34,423,924 (GRCm39) |
E594G |
probably damaging |
Het |
Mfsd12 |
T |
C |
10: 81,198,544 (GRCm39) |
L345P |
probably damaging |
Het |
Mmp24 |
A |
G |
2: 155,640,041 (GRCm39) |
R124G |
probably benign |
Het |
Ngef |
T |
A |
1: 87,406,797 (GRCm39) |
H240L |
unknown |
Het |
Nmur1 |
T |
G |
1: 86,315,256 (GRCm39) |
D203A |
probably benign |
Het |
Nt5c3 |
T |
C |
6: 56,859,955 (GRCm39) |
Q328R |
probably benign |
Het |
Ogfr |
T |
C |
2: 180,232,850 (GRCm39) |
|
probably null |
Het |
Or4k1 |
A |
T |
14: 50,377,990 (GRCm39) |
Y35* |
probably null |
Het |
Or52ac1 |
T |
A |
7: 104,245,635 (GRCm39) |
Y251F |
probably damaging |
Het |
Or5h19 |
A |
G |
16: 58,856,263 (GRCm39) |
V279A |
probably benign |
Het |
Osbpl10 |
G |
A |
9: 115,061,211 (GRCm39) |
W588* |
probably null |
Het |
Pask |
A |
T |
1: 93,265,205 (GRCm39) |
S17T |
possibly damaging |
Het |
Pfkfb3 |
C |
T |
2: 11,491,084 (GRCm39) |
R170K |
probably damaging |
Het |
Plec |
A |
G |
15: 76,069,937 (GRCm39) |
C960R |
unknown |
Het |
Pramel11 |
T |
A |
4: 143,623,646 (GRCm39) |
N176I |
probably benign |
Het |
R3hdm2 |
T |
G |
10: 127,293,521 (GRCm39) |
S142A |
probably damaging |
Het |
Rfx7 |
T |
C |
9: 72,524,163 (GRCm39) |
L451P |
probably damaging |
Het |
Rimbp2 |
T |
A |
5: 128,883,552 (GRCm39) |
E76V |
probably damaging |
Het |
Rock2 |
A |
G |
12: 17,015,557 (GRCm39) |
N818S |
probably benign |
Het |
Ryk |
A |
T |
9: 102,758,854 (GRCm39) |
I248F |
possibly damaging |
Het |
Setd2 |
A |
G |
9: 110,378,168 (GRCm39) |
Q661R |
possibly damaging |
Het |
Siae |
T |
C |
9: 37,539,105 (GRCm39) |
V172A |
probably benign |
Het |
Slc35f4 |
A |
G |
14: 49,556,377 (GRCm39) |
S9P |
unknown |
Het |
Smg1 |
T |
C |
7: 117,795,179 (GRCm39) |
E456G |
unknown |
Het |
Srgap3 |
C |
T |
6: 112,743,865 (GRCm39) |
A458T |
probably damaging |
Het |
Tgfbrap1 |
T |
A |
1: 43,093,799 (GRCm39) |
R564S |
probably damaging |
Het |
Usp15 |
A |
G |
10: 123,004,143 (GRCm39) |
Y204H |
probably damaging |
Het |
Usp8 |
T |
A |
2: 126,600,524 (GRCm39) |
*1092K |
probably null |
Het |
Vmn2r73 |
A |
T |
7: 85,518,987 (GRCm39) |
M545K |
probably benign |
Het |
Ylpm1 |
A |
T |
12: 85,080,689 (GRCm39) |
|
probably null |
Het |
Zscan22 |
G |
T |
7: 12,641,130 (GRCm39) |
R458L |
probably damaging |
Het |
|
Other mutations in Usp35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03239:Usp35
|
APN |
7 |
96,970,799 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0046:Usp35
|
UTSW |
7 |
96,962,804 (GRCm39) |
splice site |
probably null |
|
R0046:Usp35
|
UTSW |
7 |
96,962,804 (GRCm39) |
splice site |
probably null |
|
R0739:Usp35
|
UTSW |
7 |
96,960,874 (GRCm39) |
nonsense |
probably null |
|
R2655:Usp35
|
UTSW |
7 |
96,961,354 (GRCm39) |
missense |
probably benign |
|
R3623:Usp35
|
UTSW |
7 |
96,961,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R4750:Usp35
|
UTSW |
7 |
96,959,546 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4967:Usp35
|
UTSW |
7 |
96,962,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R5317:Usp35
|
UTSW |
7 |
96,960,846 (GRCm39) |
missense |
probably damaging |
0.99 |
R5341:Usp35
|
UTSW |
7 |
96,975,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5761:Usp35
|
UTSW |
7 |
96,961,558 (GRCm39) |
missense |
probably benign |
0.00 |
R5894:Usp35
|
UTSW |
7 |
96,962,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R6113:Usp35
|
UTSW |
7 |
96,973,533 (GRCm39) |
missense |
probably damaging |
1.00 |
R6282:Usp35
|
UTSW |
7 |
96,975,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6454:Usp35
|
UTSW |
7 |
96,960,851 (GRCm39) |
nonsense |
probably null |
|
R6454:Usp35
|
UTSW |
7 |
96,960,767 (GRCm39) |
missense |
probably damaging |
0.98 |
R7142:Usp35
|
UTSW |
7 |
96,960,754 (GRCm39) |
missense |
probably damaging |
0.97 |
R7158:Usp35
|
UTSW |
7 |
96,975,171 (GRCm39) |
start codon destroyed |
probably null |
0.89 |
R7260:Usp35
|
UTSW |
7 |
96,969,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R8270:Usp35
|
UTSW |
7 |
96,961,551 (GRCm39) |
missense |
probably benign |
|
R8275:Usp35
|
UTSW |
7 |
96,964,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Usp35
|
UTSW |
7 |
96,961,270 (GRCm39) |
missense |
probably benign |
|
R8795:Usp35
|
UTSW |
7 |
96,961,167 (GRCm39) |
missense |
possibly damaging |
0.92 |
RF003:Usp35
|
UTSW |
7 |
96,971,303 (GRCm39) |
missense |
possibly damaging |
0.88 |
|