Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,770,934 (GRCm39) |
L41P |
probably damaging |
Het |
Abca8a |
G |
T |
11: 109,958,878 (GRCm39) |
P749T |
probably damaging |
Het |
Acad8 |
A |
T |
9: 26,896,861 (GRCm39) |
Y199* |
probably null |
Het |
Acot12 |
A |
T |
13: 91,908,096 (GRCm39) |
I93L |
probably benign |
Het |
Acsbg3 |
T |
A |
17: 57,191,949 (GRCm39) |
Y542* |
probably null |
Het |
Actn1 |
C |
A |
12: 80,230,291 (GRCm39) |
R321L |
probably benign |
Het |
Ap3s1 |
A |
G |
18: 46,887,469 (GRCm39) |
E34G |
possibly damaging |
Het |
Armh4 |
A |
G |
14: 50,011,459 (GRCm39) |
Y83H |
probably damaging |
Het |
Atp5f1a |
T |
C |
18: 77,870,017 (GRCm39) |
S533P |
probably damaging |
Het |
Bcorl1 |
T |
C |
X: 47,458,081 (GRCm39) |
V538A |
probably benign |
Het |
Cdhr4 |
A |
G |
9: 107,875,206 (GRCm39) |
T689A |
probably damaging |
Het |
Cdk19 |
A |
T |
10: 40,355,726 (GRCm39) |
|
probably benign |
Het |
Cobll1 |
G |
T |
2: 64,928,554 (GRCm39) |
P923Q |
probably damaging |
Het |
Cpt1a |
T |
C |
19: 3,421,585 (GRCm39) |
S456P |
probably benign |
Het |
Cst11 |
T |
C |
2: 148,613,160 (GRCm39) |
Y55C |
probably damaging |
Het |
Ctif |
T |
G |
18: 75,654,452 (GRCm39) |
D358A |
probably benign |
Het |
Cyp2d34 |
T |
G |
15: 82,500,974 (GRCm39) |
E386A |
probably benign |
Het |
Dcxr |
A |
G |
11: 120,617,133 (GRCm39) |
F104L |
probably benign |
Het |
Dmbt1 |
G |
T |
7: 130,703,762 (GRCm39) |
W1107C |
probably damaging |
Het |
Dsg1a |
A |
T |
18: 20,466,830 (GRCm39) |
I567F |
probably damaging |
Het |
Ednrb |
T |
A |
14: 104,058,350 (GRCm39) |
R318* |
probably null |
Het |
Exd2 |
T |
C |
12: 80,527,377 (GRCm39) |
I36T |
possibly damaging |
Het |
Fam83b |
A |
T |
9: 76,399,987 (GRCm39) |
I372N |
probably damaging |
Het |
Fbh1 |
A |
G |
2: 11,763,100 (GRCm39) |
V518A |
probably benign |
Het |
Fkbp5 |
T |
C |
17: 28,625,162 (GRCm39) |
E308G |
possibly damaging |
Het |
Foxl2 |
A |
C |
9: 98,838,282 (GRCm39) |
Y190S |
probably damaging |
Het |
Gab3 |
TTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTC |
TTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTCTTC |
X: 74,043,585 (GRCm39) |
|
probably benign |
Het |
Galnt17 |
C |
T |
5: 131,114,831 (GRCm39) |
R223Q |
probably damaging |
Het |
Gm14496 |
G |
A |
2: 181,633,127 (GRCm39) |
D37N |
possibly damaging |
Het |
Gpr82 |
T |
C |
X: 13,532,274 (GRCm39) |
V274A |
probably benign |
Het |
Hsp90aa1 |
T |
C |
12: 110,660,566 (GRCm39) |
N292S |
probably damaging |
Het |
Ints1 |
C |
T |
5: 139,741,754 (GRCm39) |
V1826M |
possibly damaging |
Het |
Itgb4 |
A |
G |
11: 115,896,561 (GRCm39) |
D1440G |
probably benign |
Het |
Kdm3b |
A |
G |
18: 34,963,200 (GRCm39) |
D1552G |
probably damaging |
Het |
Klf3 |
T |
C |
5: 64,979,266 (GRCm39) |
V36A |
probably damaging |
Het |
Klhl23 |
A |
T |
2: 69,659,228 (GRCm39) |
I418F |
probably damaging |
Het |
Kndc1 |
A |
T |
7: 139,510,674 (GRCm39) |
I1329L |
probably benign |
Het |
Krtap2-4 |
T |
C |
11: 99,505,606 (GRCm39) |
|
probably benign |
Het |
Krtap9-5 |
T |
A |
11: 99,840,270 (GRCm39) |
C324S |
unknown |
Het |
Lepr |
T |
C |
4: 101,630,178 (GRCm39) |
V631A |
possibly damaging |
Het |
Lifr |
T |
C |
15: 7,216,404 (GRCm39) |
I793T |
probably damaging |
Het |
Mcoln1 |
G |
A |
8: 3,561,731 (GRCm39) |
R427H |
probably damaging |
Het |
Mgat5b |
G |
A |
11: 116,810,255 (GRCm39) |
|
probably benign |
Het |
Mmp12 |
G |
A |
9: 7,349,802 (GRCm39) |
V78M |
probably damaging |
Het |
Mrgprb8 |
T |
A |
7: 48,038,634 (GRCm39) |
L102M |
possibly damaging |
Het |
Mybphl |
A |
G |
3: 108,282,949 (GRCm39) |
T246A |
possibly damaging |
Het |
Myo7b |
A |
T |
18: 32,133,031 (GRCm39) |
F439L |
probably damaging |
Het |
Myom1 |
A |
T |
17: 71,408,024 (GRCm39) |
D1088V |
probably damaging |
Het |
Nrcam |
T |
C |
12: 44,623,471 (GRCm39) |
F1004S |
probably benign |
Het |
Palld |
A |
T |
8: 61,986,467 (GRCm39) |
M788K |
possibly damaging |
Het |
Pappa |
T |
A |
4: 65,234,465 (GRCm39) |
Y1423* |
probably null |
Het |
Pfkm |
A |
G |
15: 98,027,171 (GRCm39) |
K615E |
probably damaging |
Het |
Pkd1l2 |
G |
T |
8: 117,808,208 (GRCm39) |
D105E |
probably damaging |
Het |
Plekha5 |
G |
A |
6: 140,518,603 (GRCm39) |
A297T |
probably damaging |
Het |
Plxnb1 |
T |
A |
9: 108,944,810 (GRCm39) |
M2051K |
probably damaging |
Het |
Ppp6r2 |
A |
G |
15: 89,162,949 (GRCm39) |
T524A |
probably damaging |
Het |
Psg26 |
T |
C |
7: 18,209,067 (GRCm39) |
E447G |
probably damaging |
Het |
Rab3gap2 |
A |
G |
1: 185,014,586 (GRCm39) |
D1225G |
probably benign |
Het |
Rep15 |
A |
G |
6: 146,934,403 (GRCm39) |
|
probably null |
Het |
Rgl2 |
G |
A |
17: 34,152,314 (GRCm39) |
|
probably null |
Het |
Rpl7a |
T |
G |
2: 26,801,473 (GRCm39) |
V55G |
possibly damaging |
Het |
Rtp1 |
A |
T |
16: 23,250,108 (GRCm39) |
I158F |
probably benign |
Het |
Scaper |
A |
T |
9: 55,819,334 (GRCm39) |
V127E |
probably benign |
Het |
Sele |
T |
A |
1: 163,881,395 (GRCm39) |
C501S |
probably damaging |
Het |
Serpina11 |
C |
T |
12: 103,949,104 (GRCm39) |
V358I |
probably benign |
Het |
Slc16a4 |
A |
G |
3: 107,211,819 (GRCm39) |
|
probably null |
Het |
Slco6c1 |
T |
C |
1: 97,055,656 (GRCm39) |
I82V |
probably benign |
Het |
Smarca5 |
T |
C |
8: 81,431,304 (GRCm39) |
E971G |
probably damaging |
Het |
Smr2 |
T |
C |
5: 88,256,595 (GRCm39) |
L91P |
probably damaging |
Het |
Spata31f3 |
T |
A |
4: 42,868,558 (GRCm39) |
H355L |
probably benign |
Het |
Spopfm2 |
A |
T |
3: 94,082,973 (GRCm39) |
C279* |
probably null |
Het |
Srrm2 |
A |
G |
17: 24,036,722 (GRCm39) |
|
probably benign |
Het |
Sting1 |
A |
T |
18: 35,868,290 (GRCm39) |
M270K |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,006,514 (GRCm39) |
W7980R |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,074,853 (GRCm39) |
T4598A |
probably benign |
Het |
Tmem171 |
A |
T |
13: 98,828,851 (GRCm39) |
F100I |
probably damaging |
Het |
Tnfrsf10b |
A |
G |
14: 70,013,546 (GRCm39) |
T159A |
probably benign |
Het |
Tph1 |
A |
T |
7: 46,309,834 (GRCm39) |
|
probably null |
Het |
Trim46 |
A |
T |
3: 89,142,504 (GRCm39) |
I638N |
probably damaging |
Het |
Ubl7 |
G |
A |
9: 57,827,825 (GRCm39) |
D171N |
probably damaging |
Het |
Utp20 |
A |
G |
10: 88,608,779 (GRCm39) |
Y1514H |
probably damaging |
Het |
Vmn2r81 |
A |
G |
10: 79,129,334 (GRCm39) |
I742V |
probably damaging |
Het |
Xrcc2 |
A |
T |
5: 25,897,505 (GRCm39) |
V148E |
probably damaging |
Het |
Zbed3 |
A |
G |
13: 95,472,615 (GRCm39) |
D13G |
possibly damaging |
Het |
Zdhhc25 |
T |
A |
15: 88,484,962 (GRCm39) |
L99Q |
probably benign |
Het |
|
Other mutations in Kel |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00743:Kel
|
APN |
6 |
41,665,509 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00792:Kel
|
APN |
6 |
41,678,946 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00972:Kel
|
APN |
6 |
41,665,000 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL01121:Kel
|
APN |
6 |
41,679,343 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01286:Kel
|
APN |
6 |
41,665,051 (GRCm39) |
splice site |
probably null |
|
IGL01461:Kel
|
APN |
6 |
41,678,845 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01836:Kel
|
APN |
6 |
41,674,372 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02037:Kel
|
APN |
6 |
41,674,408 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02103:Kel
|
APN |
6 |
41,679,323 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02604:Kel
|
APN |
6 |
41,664,516 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03102:Kel
|
APN |
6 |
41,679,917 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03274:Kel
|
APN |
6 |
41,664,929 (GRCm39) |
splice site |
probably null |
|
IGL03355:Kel
|
APN |
6 |
41,675,821 (GRCm39) |
critical splice donor site |
probably null |
|
A4554:Kel
|
UTSW |
6 |
41,674,353 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0121:Kel
|
UTSW |
6 |
41,678,998 (GRCm39) |
unclassified |
probably benign |
|
R0153:Kel
|
UTSW |
6 |
41,678,877 (GRCm39) |
missense |
probably benign |
0.08 |
R0535:Kel
|
UTSW |
6 |
41,667,772 (GRCm39) |
missense |
probably null |
0.21 |
R0658:Kel
|
UTSW |
6 |
41,679,965 (GRCm39) |
missense |
probably damaging |
1.00 |
R1005:Kel
|
UTSW |
6 |
41,665,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R1199:Kel
|
UTSW |
6 |
41,665,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1272:Kel
|
UTSW |
6 |
41,680,404 (GRCm39) |
missense |
probably benign |
0.00 |
R1531:Kel
|
UTSW |
6 |
41,665,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R1880:Kel
|
UTSW |
6 |
41,664,479 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2118:Kel
|
UTSW |
6 |
41,666,234 (GRCm39) |
missense |
probably benign |
|
R2571:Kel
|
UTSW |
6 |
41,665,001 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4209:Kel
|
UTSW |
6 |
41,675,359 (GRCm39) |
nonsense |
probably null |
|
R4210:Kel
|
UTSW |
6 |
41,675,359 (GRCm39) |
nonsense |
probably null |
|
R4260:Kel
|
UTSW |
6 |
41,663,357 (GRCm39) |
utr 3 prime |
probably benign |
|
R4382:Kel
|
UTSW |
6 |
41,675,334 (GRCm39) |
missense |
probably benign |
0.13 |
R5023:Kel
|
UTSW |
6 |
41,665,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Kel
|
UTSW |
6 |
41,675,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Kel
|
UTSW |
6 |
41,665,048 (GRCm39) |
nonsense |
probably null |
|
R5431:Kel
|
UTSW |
6 |
41,675,354 (GRCm39) |
missense |
probably benign |
0.23 |
R5742:Kel
|
UTSW |
6 |
41,675,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5745:Kel
|
UTSW |
6 |
41,675,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5746:Kel
|
UTSW |
6 |
41,675,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R5978:Kel
|
UTSW |
6 |
41,664,979 (GRCm39) |
missense |
probably benign |
0.00 |
R6023:Kel
|
UTSW |
6 |
41,674,409 (GRCm39) |
missense |
probably benign |
|
R6109:Kel
|
UTSW |
6 |
41,665,796 (GRCm39) |
missense |
probably benign |
0.06 |
R6125:Kel
|
UTSW |
6 |
41,667,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R6319:Kel
|
UTSW |
6 |
41,679,381 (GRCm39) |
missense |
probably benign |
0.05 |
R6368:Kel
|
UTSW |
6 |
41,665,785 (GRCm39) |
nonsense |
probably null |
|
R6864:Kel
|
UTSW |
6 |
41,680,694 (GRCm39) |
critical splice donor site |
probably null |
|
R6956:Kel
|
UTSW |
6 |
41,664,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R7644:Kel
|
UTSW |
6 |
41,667,742 (GRCm39) |
missense |
probably benign |
0.03 |
R7938:Kel
|
UTSW |
6 |
41,675,310 (GRCm39) |
missense |
probably benign |
0.06 |
R8028:Kel
|
UTSW |
6 |
41,675,958 (GRCm39) |
missense |
probably benign |
0.21 |
R8082:Kel
|
UTSW |
6 |
41,680,424 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8465:Kel
|
UTSW |
6 |
41,666,472 (GRCm39) |
critical splice donor site |
probably null |
|
R9158:Kel
|
UTSW |
6 |
41,664,905 (GRCm39) |
missense |
probably benign |
0.10 |
R9518:Kel
|
UTSW |
6 |
41,679,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R9726:Kel
|
UTSW |
6 |
41,678,971 (GRCm39) |
missense |
probably damaging |
1.00 |
R9769:Kel
|
UTSW |
6 |
41,678,990 (GRCm39) |
missense |
probably damaging |
1.00 |
X0028:Kel
|
UTSW |
6 |
41,675,285 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Kel
|
UTSW |
6 |
41,664,506 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Kel
|
UTSW |
6 |
41,666,493 (GRCm39) |
missense |
probably benign |
|
|