Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
C |
11: 9,401,333 (GRCm39) |
|
probably benign |
Het |
Adamts6 |
A |
T |
13: 104,563,485 (GRCm39) |
Y659F |
probably benign |
Het |
Adamts9 |
C |
A |
6: 92,834,881 (GRCm39) |
G750W |
probably damaging |
Het |
Adgrv1 |
GA |
GAA |
13: 81,688,251 (GRCm39) |
|
probably null |
Het |
Aspscr1 |
A |
G |
11: 120,593,392 (GRCm39) |
|
probably benign |
Het |
Calr3 |
A |
G |
8: 73,192,270 (GRCm39) |
|
probably benign |
Het |
Cpt2 |
A |
T |
4: 107,761,723 (GRCm39) |
Y126* |
probably null |
Het |
Cyp2d34 |
A |
G |
15: 82,503,212 (GRCm39) |
L94P |
probably damaging |
Het |
Def6 |
A |
T |
17: 28,447,043 (GRCm39) |
D558V |
probably benign |
Het |
Dnase1l2 |
G |
A |
17: 24,661,699 (GRCm39) |
T20I |
possibly damaging |
Het |
Eif5b |
A |
G |
1: 38,058,423 (GRCm39) |
K242E |
unknown |
Het |
Golim4 |
T |
C |
3: 75,799,249 (GRCm39) |
N478S |
possibly damaging |
Het |
Helb |
A |
T |
10: 119,941,442 (GRCm39) |
D415E |
probably benign |
Het |
Ifna12 |
T |
A |
4: 88,521,590 (GRCm39) |
|
probably benign |
Het |
Jhy |
T |
A |
9: 40,872,182 (GRCm39) |
H109L |
probably benign |
Het |
Krt87 |
A |
T |
15: 101,386,037 (GRCm39) |
Y241* |
probably null |
Het |
Macf1 |
G |
T |
4: 123,577,789 (GRCm39) |
A65E |
probably damaging |
Het |
Mug2 |
C |
A |
6: 122,061,335 (GRCm39) |
N1418K |
possibly damaging |
Het |
Myo1f |
A |
G |
17: 33,794,823 (GRCm39) |
D21G |
probably damaging |
Het |
Myo5a |
T |
A |
9: 75,120,155 (GRCm39) |
I1651N |
possibly damaging |
Het |
Notch3 |
A |
T |
17: 32,372,778 (GRCm39) |
C598S |
probably damaging |
Het |
Npat |
A |
T |
9: 53,469,435 (GRCm39) |
H307L |
probably damaging |
Het |
Nr1h2 |
T |
C |
7: 44,200,791 (GRCm39) |
Q279R |
possibly damaging |
Het |
Or4k52 |
T |
C |
2: 111,611,016 (GRCm39) |
V117A |
probably benign |
Het |
Or6c6c |
A |
G |
10: 129,540,794 (GRCm39) |
T16A |
possibly damaging |
Het |
Pcdhb16 |
A |
T |
18: 37,612,983 (GRCm39) |
N648Y |
probably damaging |
Het |
Pdzrn3 |
G |
T |
6: 101,127,752 (GRCm39) |
S971R |
probably damaging |
Het |
Plch2 |
A |
G |
4: 155,070,621 (GRCm39) |
*494Q |
probably null |
Het |
Plekhg4 |
T |
A |
8: 106,108,468 (GRCm39) |
D1170E |
probably benign |
Het |
Plekhm3 |
A |
G |
1: 64,977,015 (GRCm39) |
S152P |
probably damaging |
Het |
Ppargc1b |
G |
A |
18: 61,440,870 (GRCm39) |
P683S |
possibly damaging |
Het |
Prdm12 |
T |
G |
2: 31,541,864 (GRCm39) |
M191R |
probably benign |
Het |
Prdm14 |
T |
C |
1: 13,195,857 (GRCm39) |
D68G |
probably benign |
Het |
Prpf4b |
A |
G |
13: 35,067,324 (GRCm39) |
|
probably benign |
Het |
Ptprk |
T |
A |
10: 28,468,840 (GRCm39) |
V1408E |
probably damaging |
Het |
Rap1gds1 |
A |
G |
3: 138,662,011 (GRCm39) |
M415T |
probably damaging |
Het |
Rps6ka5 |
A |
G |
12: 100,520,664 (GRCm39) |
F621S |
probably damaging |
Het |
Rrm1 |
T |
A |
7: 102,092,279 (GRCm39) |
D35E |
probably benign |
Het |
Rxfp3 |
T |
C |
15: 11,036,226 (GRCm39) |
H382R |
probably damaging |
Het |
Slc11a1 |
A |
G |
1: 74,422,910 (GRCm39) |
|
probably benign |
Het |
Slc25a13 |
A |
T |
6: 6,114,017 (GRCm39) |
M285K |
probably benign |
Het |
Slc30a3 |
T |
C |
5: 31,246,038 (GRCm39) |
S231G |
probably damaging |
Het |
Slc44a2 |
A |
T |
9: 21,256,130 (GRCm39) |
I274F |
probably damaging |
Het |
Tas2r119 |
A |
G |
15: 32,178,165 (GRCm39) |
I244V |
possibly damaging |
Het |
Tenm2 |
C |
A |
11: 35,918,018 (GRCm39) |
R1914L |
probably damaging |
Het |
Tfdp2 |
T |
C |
9: 96,192,643 (GRCm39) |
M242T |
probably damaging |
Het |
Tmprss6 |
A |
G |
15: 78,349,304 (GRCm39) |
|
probably benign |
Het |
Ttc6 |
C |
T |
12: 57,668,821 (GRCm39) |
P421L |
possibly damaging |
Het |
Usp16 |
T |
A |
16: 87,263,246 (GRCm39) |
|
probably null |
Het |
Usp40 |
T |
C |
1: 87,909,804 (GRCm39) |
E550G |
probably benign |
Het |
Vmn2r28 |
T |
C |
7: 5,491,701 (GRCm39) |
Y182C |
probably damaging |
Het |
Zfp382 |
A |
G |
7: 29,833,174 (GRCm39) |
D275G |
probably benign |
Het |
|
Other mutations in Prp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01383:Prp2
|
APN |
6 |
132,576,841 (GRCm39) |
missense |
unknown |
|
IGL02951:Prp2
|
APN |
6 |
132,576,788 (GRCm39) |
missense |
unknown |
|
PIT4458001:Prp2
|
UTSW |
6 |
132,577,510 (GRCm39) |
missense |
unknown |
|
R2034:Prp2
|
UTSW |
6 |
132,572,947 (GRCm39) |
splice site |
probably null |
|
R5283:Prp2
|
UTSW |
6 |
132,577,606 (GRCm39) |
missense |
unknown |
|
R7761:Prp2
|
UTSW |
6 |
132,577,306 (GRCm39) |
nonsense |
probably null |
|
R7877:Prp2
|
UTSW |
6 |
132,572,928 (GRCm39) |
missense |
unknown |
|
R8033:Prp2
|
UTSW |
6 |
132,577,391 (GRCm39) |
missense |
unknown |
|
R8062:Prp2
|
UTSW |
6 |
132,577,651 (GRCm39) |
missense |
unknown |
|
R8695:Prp2
|
UTSW |
6 |
132,576,932 (GRCm39) |
missense |
unknown |
|
R8696:Prp2
|
UTSW |
6 |
132,577,322 (GRCm39) |
missense |
unknown |
|
R8938:Prp2
|
UTSW |
6 |
132,577,581 (GRCm39) |
missense |
unknown |
|
RF005:Prp2
|
UTSW |
6 |
132,577,464 (GRCm39) |
small deletion |
probably benign |
|
RF016:Prp2
|
UTSW |
6 |
132,577,475 (GRCm39) |
small deletion |
probably benign |
|
RF039:Prp2
|
UTSW |
6 |
132,577,464 (GRCm39) |
small deletion |
probably benign |
|
RF052:Prp2
|
UTSW |
6 |
132,577,475 (GRCm39) |
small deletion |
probably benign |
|
RF054:Prp2
|
UTSW |
6 |
132,577,484 (GRCm39) |
frame shift |
probably null |
|
RF057:Prp2
|
UTSW |
6 |
132,577,493 (GRCm39) |
frame shift |
probably null |
|
X0053:Prp2
|
UTSW |
6 |
132,577,559 (GRCm39) |
missense |
unknown |
|
Z1176:Prp2
|
UTSW |
6 |
132,577,200 (GRCm39) |
missense |
unknown |
|
Z1177:Prp2
|
UTSW |
6 |
132,572,933 (GRCm39) |
missense |
unknown |
|
|