Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
4933409G03Rik |
G |
A |
2: 68,436,559 (GRCm39) |
E168K |
unknown |
Het |
Ahnak2 |
T |
G |
12: 112,741,271 (GRCm39) |
S128R |
possibly damaging |
Het |
Ankrd26 |
T |
C |
6: 118,492,787 (GRCm39) |
D1319G |
probably benign |
Het |
Ankrd35 |
T |
C |
3: 96,591,343 (GRCm39) |
V543A |
probably benign |
Het |
Ano10 |
A |
T |
9: 122,090,181 (GRCm39) |
Y377* |
probably null |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Atp10b |
G |
A |
11: 43,085,472 (GRCm39) |
G284S |
probably damaging |
Het |
Atp5f1c |
A |
G |
2: 10,068,287 (GRCm39) |
F180S |
probably damaging |
Het |
Btnl4 |
A |
G |
17: 34,691,602 (GRCm39) |
S296P |
probably benign |
Het |
Cast |
A |
G |
13: 74,894,133 (GRCm39) |
S171P |
probably benign |
Het |
Catsperb |
G |
A |
12: 101,507,771 (GRCm39) |
A513T |
probably benign |
Het |
Ccnf |
C |
A |
17: 24,450,760 (GRCm39) |
R406L |
probably damaging |
Het |
Ceacam12 |
A |
G |
7: 17,801,359 (GRCm39) |
T113A |
probably damaging |
Het |
Cipc |
T |
C |
12: 87,008,864 (GRCm39) |
V241A |
probably benign |
Het |
Col12a1 |
A |
T |
9: 79,520,228 (GRCm39) |
D2815E |
probably damaging |
Het |
Cpox |
G |
T |
16: 58,491,050 (GRCm39) |
R87L |
possibly damaging |
Het |
Cttnbp2 |
A |
G |
6: 18,434,037 (GRCm39) |
I607T |
possibly damaging |
Het |
Cux1 |
A |
T |
5: 136,596,083 (GRCm39) |
N4K |
probably damaging |
Het |
Cyp3a25 |
T |
C |
5: 145,931,701 (GRCm39) |
T136A |
probably benign |
Het |
Dhx58 |
T |
A |
11: 100,592,185 (GRCm39) |
N288Y |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,806,207 (GRCm39) |
Y127H |
probably benign |
Het |
Dnd1 |
G |
A |
18: 36,898,114 (GRCm39) |
|
probably benign |
Het |
Ehmt2 |
C |
A |
17: 35,132,790 (GRCm39) |
N1171K |
probably damaging |
Het |
Fanci |
T |
A |
7: 79,085,004 (GRCm39) |
M838K |
possibly damaging |
Het |
Flot1 |
T |
C |
17: 36,143,436 (GRCm39) |
|
probably benign |
Het |
Gad2 |
A |
T |
2: 22,558,374 (GRCm39) |
D364V |
probably damaging |
Het |
Gm10375 |
C |
A |
14: 43,844,326 (GRCm39) |
|
probably null |
Het |
Gm9996 |
T |
A |
10: 29,019,754 (GRCm39) |
|
probably benign |
Het |
Gnat3 |
T |
A |
5: 18,220,568 (GRCm39) |
L247H |
probably damaging |
Het |
Ip6k3 |
C |
T |
17: 27,364,265 (GRCm39) |
C261Y |
probably damaging |
Het |
Irgc |
C |
A |
7: 24,132,238 (GRCm39) |
R193L |
probably damaging |
Het |
Kalrn |
G |
T |
16: 33,996,761 (GRCm39) |
P1477Q |
probably damaging |
Het |
Kyat1 |
G |
T |
2: 30,084,076 (GRCm39) |
H15N |
probably benign |
Het |
Lamc1 |
T |
G |
1: 153,104,523 (GRCm39) |
S59R |
probably damaging |
Het |
Llgl1 |
A |
G |
11: 60,599,477 (GRCm39) |
D486G |
possibly damaging |
Het |
Lrrc9 |
T |
C |
12: 72,524,160 (GRCm39) |
W790R |
probably damaging |
Het |
Lsm2 |
T |
A |
17: 35,204,571 (GRCm39) |
|
probably benign |
Het |
Med8 |
A |
T |
4: 118,268,089 (GRCm39) |
E5V |
probably damaging |
Het |
Mefv |
A |
G |
16: 3,535,682 (GRCm39) |
L82P |
probably damaging |
Het |
Mettl25b |
T |
C |
3: 87,834,979 (GRCm39) |
H107R |
probably benign |
Het |
Mettl3 |
T |
A |
14: 52,532,549 (GRCm39) |
I545F |
probably damaging |
Het |
Naa20 |
CTCTAGA |
C |
2: 145,753,752 (GRCm39) |
|
probably benign |
Het |
Ncapg2 |
T |
A |
12: 116,389,407 (GRCm39) |
N342K |
probably damaging |
Het |
Ndufaf6 |
T |
A |
4: 11,062,070 (GRCm39) |
Y187F |
probably damaging |
Het |
Nomo1 |
T |
A |
7: 45,717,866 (GRCm39) |
I799N |
probably damaging |
Het |
Obscn |
G |
A |
11: 58,929,703 (GRCm39) |
R5824C |
probably damaging |
Het |
Or4f6 |
G |
T |
2: 111,838,595 (GRCm39) |
S312Y |
probably damaging |
Het |
Or6c214 |
T |
C |
10: 129,591,287 (GRCm39) |
I11V |
probably benign |
Het |
Or6n2 |
A |
G |
1: 173,897,394 (GRCm39) |
I177V |
possibly damaging |
Het |
Or7g30 |
T |
A |
9: 19,352,591 (GRCm39) |
C127* |
probably null |
Het |
Pgm3 |
T |
A |
9: 86,440,523 (GRCm39) |
R389S |
probably benign |
Het |
Pkd2l2 |
A |
T |
18: 34,542,889 (GRCm39) |
R20* |
probably null |
Het |
Pkhd1 |
T |
A |
1: 20,451,747 (GRCm39) |
I2183F |
probably damaging |
Het |
Ppp4r3a |
T |
A |
12: 101,049,170 (GRCm39) |
|
probably benign |
Het |
Prpf38b |
G |
A |
3: 108,811,408 (GRCm39) |
|
probably benign |
Het |
Prps2 |
T |
C |
X: 166,135,288 (GRCm39) |
D183G |
probably damaging |
Het |
Prrc2c |
A |
T |
1: 162,550,843 (GRCm39) |
H40Q |
probably damaging |
Het |
Ptprk |
T |
C |
10: 28,139,686 (GRCm39) |
I137T |
probably damaging |
Het |
Sdr42e1 |
T |
C |
8: 118,390,360 (GRCm39) |
T94A |
probably benign |
Het |
Setd2 |
A |
G |
9: 110,423,200 (GRCm39) |
D2085G |
possibly damaging |
Het |
Sgce |
T |
C |
6: 4,689,560 (GRCm39) |
|
probably benign |
Het |
Shisa3 |
A |
G |
5: 67,765,992 (GRCm39) |
D81G |
probably damaging |
Het |
Sipa1l1 |
T |
A |
12: 82,469,245 (GRCm39) |
L1248* |
probably null |
Het |
Skint7 |
T |
G |
4: 111,839,309 (GRCm39) |
M201R |
probably damaging |
Het |
Slc5a3 |
T |
A |
16: 91,874,090 (GRCm39) |
V49E |
probably benign |
Het |
Slc9c1 |
A |
T |
16: 45,367,756 (GRCm39) |
*163L |
probably null |
Het |
Smyd3 |
A |
G |
1: 178,871,306 (GRCm39) |
Y358H |
probably benign |
Het |
Srp68 |
A |
T |
11: 116,164,840 (GRCm39) |
S31R |
probably benign |
Het |
Stag1 |
T |
A |
9: 100,678,769 (GRCm39) |
M230K |
probably damaging |
Het |
Strc |
A |
T |
2: 121,204,829 (GRCm39) |
D985E |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,036,013 (GRCm39) |
T3767A |
probably damaging |
Het |
Sytl2 |
C |
A |
7: 90,024,633 (GRCm39) |
P207Q |
probably damaging |
Het |
Tbc1d2b |
A |
G |
9: 90,089,940 (GRCm39) |
F863S |
probably damaging |
Het |
Tek |
T |
C |
4: 94,669,121 (GRCm39) |
S41P |
probably damaging |
Het |
Top1 |
T |
C |
2: 160,554,637 (GRCm39) |
Y463H |
probably damaging |
Het |
Trim24 |
T |
G |
6: 37,934,774 (GRCm39) |
|
probably null |
Het |
Trim38 |
A |
T |
13: 23,966,952 (GRCm39) |
D133V |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,576,979 (GRCm39) |
V24638A |
possibly damaging |
Het |
Ttn |
A |
G |
2: 76,701,213 (GRCm39) |
|
probably benign |
Het |
Tyro3 |
G |
C |
2: 119,647,349 (GRCm39) |
G826A |
probably benign |
Het |
Ube2b |
A |
G |
11: 51,886,199 (GRCm39) |
|
probably null |
Het |
Ubxn4 |
T |
A |
1: 128,202,587 (GRCm39) |
W410R |
probably benign |
Het |
Unc45a |
T |
C |
7: 79,982,777 (GRCm39) |
K383E |
possibly damaging |
Het |
Usp7 |
A |
C |
16: 8,516,278 (GRCm39) |
|
probably benign |
Het |
Vmn1r193 |
C |
T |
13: 22,403,695 (GRCm39) |
G99D |
probably damaging |
Het |
Vrk2 |
T |
C |
11: 26,439,803 (GRCm39) |
D256G |
probably damaging |
Het |
Wdr81 |
A |
G |
11: 75,342,066 (GRCm39) |
V1067A |
probably damaging |
Het |
Wiz |
C |
T |
17: 32,576,655 (GRCm39) |
R624Q |
probably damaging |
Het |
Zcwpw2 |
A |
G |
9: 117,843,119 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Prpf4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Prpf4b
|
APN |
13 |
35,067,890 (GRCm39) |
missense |
probably benign |
0.23 |
IGL00639:Prpf4b
|
APN |
13 |
35,083,156 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL00901:Prpf4b
|
APN |
13 |
35,078,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01301:Prpf4b
|
APN |
13 |
35,068,274 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02027:Prpf4b
|
APN |
13 |
35,073,554 (GRCm39) |
missense |
probably benign |
0.35 |
IGL02111:Prpf4b
|
APN |
13 |
35,067,944 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02256:Prpf4b
|
APN |
13 |
35,083,861 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02590:Prpf4b
|
APN |
13 |
35,072,129 (GRCm39) |
unclassified |
probably benign |
|
IGL03389:Prpf4b
|
APN |
13 |
35,084,439 (GRCm39) |
splice site |
probably benign |
|
IGL03411:Prpf4b
|
APN |
13 |
35,079,342 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU18:Prpf4b
|
UTSW |
13 |
35,068,274 (GRCm39) |
missense |
probably benign |
0.23 |
PIT4260001:Prpf4b
|
UTSW |
13 |
35,068,274 (GRCm39) |
missense |
probably benign |
0.23 |
PIT4696001:Prpf4b
|
UTSW |
13 |
35,083,825 (GRCm39) |
missense |
probably benign |
0.01 |
R0114:Prpf4b
|
UTSW |
13 |
35,074,471 (GRCm39) |
splice site |
probably benign |
|
R0157:Prpf4b
|
UTSW |
13 |
35,068,014 (GRCm39) |
unclassified |
probably benign |
|
R1551:Prpf4b
|
UTSW |
13 |
35,078,426 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1587:Prpf4b
|
UTSW |
13 |
35,076,133 (GRCm39) |
missense |
probably benign |
0.09 |
R2105:Prpf4b
|
UTSW |
13 |
35,068,214 (GRCm39) |
unclassified |
probably benign |
|
R2152:Prpf4b
|
UTSW |
13 |
35,084,402 (GRCm39) |
missense |
probably benign |
0.04 |
R2432:Prpf4b
|
UTSW |
13 |
35,067,324 (GRCm39) |
unclassified |
probably benign |
|
R3802:Prpf4b
|
UTSW |
13 |
35,067,665 (GRCm39) |
unclassified |
probably benign |
|
R3803:Prpf4b
|
UTSW |
13 |
35,067,665 (GRCm39) |
unclassified |
probably benign |
|
R3804:Prpf4b
|
UTSW |
13 |
35,067,665 (GRCm39) |
unclassified |
probably benign |
|
R3982:Prpf4b
|
UTSW |
13 |
35,068,196 (GRCm39) |
unclassified |
probably benign |
|
R4603:Prpf4b
|
UTSW |
13 |
35,072,147 (GRCm39) |
unclassified |
probably benign |
|
R4633:Prpf4b
|
UTSW |
13 |
35,084,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Prpf4b
|
UTSW |
13 |
35,083,954 (GRCm39) |
missense |
probably benign |
0.06 |
R4653:Prpf4b
|
UTSW |
13 |
35,083,954 (GRCm39) |
missense |
probably benign |
0.06 |
R5022:Prpf4b
|
UTSW |
13 |
35,067,582 (GRCm39) |
unclassified |
probably benign |
|
R5028:Prpf4b
|
UTSW |
13 |
35,083,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R5232:Prpf4b
|
UTSW |
13 |
35,067,573 (GRCm39) |
unclassified |
probably benign |
|
R5313:Prpf4b
|
UTSW |
13 |
35,078,532 (GRCm39) |
missense |
probably damaging |
1.00 |
R5440:Prpf4b
|
UTSW |
13 |
35,068,076 (GRCm39) |
unclassified |
probably benign |
|
R5511:Prpf4b
|
UTSW |
13 |
35,068,037 (GRCm39) |
unclassified |
probably benign |
|
R5863:Prpf4b
|
UTSW |
13 |
35,083,111 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5981:Prpf4b
|
UTSW |
13 |
35,070,693 (GRCm39) |
missense |
probably benign |
0.23 |
R6360:Prpf4b
|
UTSW |
13 |
35,085,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R6398:Prpf4b
|
UTSW |
13 |
35,084,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R6556:Prpf4b
|
UTSW |
13 |
35,080,015 (GRCm39) |
missense |
probably damaging |
0.98 |
R6880:Prpf4b
|
UTSW |
13 |
35,078,436 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7133:Prpf4b
|
UTSW |
13 |
35,085,477 (GRCm39) |
missense |
probably benign |
0.02 |
R7148:Prpf4b
|
UTSW |
13 |
35,078,455 (GRCm39) |
missense |
probably benign |
0.04 |
R7208:Prpf4b
|
UTSW |
13 |
35,067,994 (GRCm39) |
missense |
unknown |
|
R7966:Prpf4b
|
UTSW |
13 |
35,085,428 (GRCm39) |
missense |
probably damaging |
0.96 |
R8241:Prpf4b
|
UTSW |
13 |
35,079,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R8298:Prpf4b
|
UTSW |
13 |
35,072,166 (GRCm39) |
missense |
unknown |
|
R9609:Prpf4b
|
UTSW |
13 |
35,068,032 (GRCm39) |
missense |
unknown |
|
R9710:Prpf4b
|
UTSW |
13 |
35,083,870 (GRCm39) |
missense |
probably damaging |
1.00 |
RF002:Prpf4b
|
UTSW |
13 |
35,068,219 (GRCm39) |
missense |
unknown |
|
|