Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
G |
A |
4: 144,396,683 (GRCm39) |
R350C |
possibly damaging |
Het |
Acsm3 |
T |
A |
7: 119,374,392 (GRCm39) |
S281R |
probably damaging |
Het |
Adipor2 |
G |
T |
6: 119,340,447 (GRCm39) |
|
probably benign |
Het |
Alk |
T |
C |
17: 72,204,936 (GRCm39) |
S1079G |
probably damaging |
Het |
Ankrd27 |
T |
C |
7: 35,302,009 (GRCm39) |
|
probably null |
Het |
Anxa6 |
C |
A |
11: 54,892,108 (GRCm39) |
E283* |
probably null |
Het |
Bnc2 |
T |
C |
4: 84,194,550 (GRCm39) |
H858R |
possibly damaging |
Het |
Btnl6 |
T |
C |
17: 34,727,043 (GRCm39) |
S496G |
probably benign |
Het |
Ccdc88a |
T |
C |
11: 29,410,860 (GRCm39) |
S449P |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,246,689 (GRCm39) |
D916E |
probably damaging |
Het |
Cfap43 |
A |
T |
19: 47,736,456 (GRCm39) |
L1345H |
possibly damaging |
Het |
Cyld |
A |
T |
8: 89,456,138 (GRCm39) |
H396L |
probably benign |
Het |
Cyp20a1 |
A |
G |
1: 60,418,579 (GRCm39) |
T340A |
possibly damaging |
Het |
Czib |
A |
G |
4: 107,752,796 (GRCm39) |
N152D |
unknown |
Het |
Dera |
A |
T |
6: 137,807,202 (GRCm39) |
I217F |
probably damaging |
Het |
Dnah11 |
A |
G |
12: 118,154,539 (GRCm39) |
L247P |
probably damaging |
Het |
Eftud2 |
G |
A |
11: 102,759,447 (GRCm39) |
T152M |
probably damaging |
Het |
Entrep1 |
T |
C |
19: 23,965,858 (GRCm39) |
K214E |
probably damaging |
Het |
Epb41l2 |
C |
T |
10: 25,319,674 (GRCm39) |
T169M |
probably benign |
Het |
Gli3 |
T |
A |
13: 15,889,619 (GRCm39) |
C578S |
probably damaging |
Het |
Gm6408 |
A |
G |
5: 146,419,237 (GRCm39) |
N84S |
probably benign |
Het |
Heatr5a |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGTGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
AGCACACTGCAGGAAGCTCACACAGCACAGCATACCTTCAGGAGAGCACACTGCAGGAAGCTCA |
12: 51,934,702 (GRCm39) |
|
probably benign |
Het |
Herc2 |
C |
A |
7: 55,838,361 (GRCm39) |
T3296K |
probably damaging |
Het |
Hnf4g |
A |
T |
3: 3,708,133 (GRCm39) |
|
probably benign |
Het |
Hyal4 |
C |
A |
6: 24,755,826 (GRCm39) |
Q15K |
probably damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kcna3 |
A |
G |
3: 106,943,908 (GRCm39) |
E57G |
probably damaging |
Het |
Kcnc3 |
C |
A |
7: 44,241,020 (GRCm39) |
D237E |
probably benign |
Het |
Map3k8 |
A |
G |
18: 4,343,137 (GRCm39) |
V130A |
probably benign |
Het |
Mpp7 |
A |
G |
18: 7,440,430 (GRCm39) |
|
probably null |
Het |
Mtres1 |
A |
G |
10: 43,408,933 (GRCm39) |
L70S |
probably benign |
Het |
Myh13 |
T |
A |
11: 67,233,311 (GRCm39) |
L610Q |
probably damaging |
Het |
Or13p5 |
C |
A |
4: 118,592,235 (GRCm39) |
P170T |
probably damaging |
Het |
Or5ap2 |
T |
A |
2: 85,680,246 (GRCm39) |
M150K |
probably benign |
Het |
Or8b52 |
T |
C |
9: 38,577,064 (GRCm39) |
I25M |
probably benign |
Het |
Pcdhb5 |
A |
T |
18: 37,454,129 (GRCm39) |
T170S |
probably benign |
Het |
Polr3b |
T |
A |
10: 84,516,251 (GRCm39) |
H626Q |
probably benign |
Het |
Prkg1 |
A |
T |
19: 31,742,146 (GRCm39) |
L26Q |
probably damaging |
Het |
Prob1 |
T |
C |
18: 35,787,039 (GRCm39) |
N405S |
possibly damaging |
Het |
Proz |
T |
G |
8: 13,123,630 (GRCm39) |
S300R |
probably damaging |
Het |
Psg19 |
A |
G |
7: 18,527,990 (GRCm39) |
I251T |
probably benign |
Het |
Rcbtb1 |
T |
C |
14: 59,467,401 (GRCm39) |
I413T |
possibly damaging |
Het |
Rnf144b |
T |
A |
13: 47,382,452 (GRCm39) |
Y103N |
probably damaging |
Het |
Rspry1 |
G |
C |
8: 95,358,747 (GRCm39) |
G194R |
probably benign |
Het |
Scn2b |
A |
G |
9: 45,036,917 (GRCm39) |
I142V |
probably damaging |
Het |
Spata20 |
A |
T |
11: 94,372,607 (GRCm39) |
L588H |
probably damaging |
Het |
Stk32b |
T |
A |
5: 37,614,503 (GRCm39) |
H335L |
probably benign |
Het |
Taar4 |
A |
C |
10: 23,836,801 (GRCm39) |
D137A |
possibly damaging |
Het |
Tchh |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC |
3: 93,354,015 (GRCm39) |
|
probably benign |
Het |
Tek |
A |
T |
4: 94,738,074 (GRCm39) |
H708L |
probably benign |
Het |
Tmem89 |
C |
T |
9: 108,744,095 (GRCm39) |
L132F |
unknown |
Het |
Ugt2b38 |
T |
C |
5: 87,559,681 (GRCm39) |
I404V |
probably benign |
Het |
Vmn1r16 |
C |
T |
6: 57,299,814 (GRCm39) |
M269I |
probably benign |
Het |
Vmn1r201 |
A |
G |
13: 22,659,422 (GRCm39) |
K212R |
probably damaging |
Het |
Vmn2r11 |
A |
C |
5: 109,201,626 (GRCm39) |
F293V |
probably damaging |
Het |
Zdhhc17 |
A |
T |
10: 110,798,240 (GRCm39) |
|
probably benign |
Het |
Zfp423 |
C |
A |
8: 88,509,338 (GRCm39) |
M335I |
probably benign |
Het |
Zfp74 |
T |
C |
7: 29,634,079 (GRCm39) |
Y543C |
probably damaging |
Het |
Zfp975 |
A |
T |
7: 42,312,264 (GRCm39) |
S116R |
probably benign |
Het |
|
Other mutations in Fam186a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00588:Fam186a
|
APN |
15 |
99,825,572 (GRCm39) |
splice site |
probably benign |
|
IGL03047:Fam186a
|
UTSW |
15 |
99,843,589 (GRCm39) |
missense |
unknown |
|
R0172:Fam186a
|
UTSW |
15 |
99,852,768 (GRCm39) |
missense |
unknown |
|
R0194:Fam186a
|
UTSW |
15 |
99,839,644 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0381:Fam186a
|
UTSW |
15 |
99,840,055 (GRCm39) |
missense |
probably damaging |
0.97 |
R0799:Fam186a
|
UTSW |
15 |
99,839,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Fam186a
|
UTSW |
15 |
99,837,670 (GRCm39) |
splice site |
probably benign |
|
R1366:Fam186a
|
UTSW |
15 |
99,841,270 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1519:Fam186a
|
UTSW |
15 |
99,845,536 (GRCm39) |
missense |
unknown |
|
R1592:Fam186a
|
UTSW |
15 |
99,838,199 (GRCm39) |
missense |
probably benign |
0.01 |
R1636:Fam186a
|
UTSW |
15 |
99,839,539 (GRCm39) |
missense |
unknown |
|
R1719:Fam186a
|
UTSW |
15 |
99,840,227 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1759:Fam186a
|
UTSW |
15 |
99,864,762 (GRCm39) |
nonsense |
probably null |
|
R1856:Fam186a
|
UTSW |
15 |
99,838,183 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2131:Fam186a
|
UTSW |
15 |
99,831,557 (GRCm39) |
unclassified |
probably benign |
|
R2192:Fam186a
|
UTSW |
15 |
99,838,192 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2239:Fam186a
|
UTSW |
15 |
99,852,745 (GRCm39) |
missense |
unknown |
|
R2251:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.02 |
R2902:Fam186a
|
UTSW |
15 |
99,843,049 (GRCm39) |
missense |
possibly damaging |
0.73 |
R3037:Fam186a
|
UTSW |
15 |
99,841,675 (GRCm39) |
missense |
probably damaging |
0.99 |
R3744:Fam186a
|
UTSW |
15 |
99,845,416 (GRCm39) |
missense |
unknown |
|
R4021:Fam186a
|
UTSW |
15 |
99,839,680 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4183:Fam186a
|
UTSW |
15 |
99,831,566 (GRCm39) |
unclassified |
probably benign |
|
R4238:Fam186a
|
UTSW |
15 |
99,841,523 (GRCm39) |
missense |
probably benign |
0.05 |
R4667:Fam186a
|
UTSW |
15 |
99,842,413 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4817:Fam186a
|
UTSW |
15 |
99,831,419 (GRCm39) |
unclassified |
probably benign |
|
R4835:Fam186a
|
UTSW |
15 |
99,843,689 (GRCm39) |
missense |
unknown |
|
R4837:Fam186a
|
UTSW |
15 |
99,838,678 (GRCm39) |
missense |
unknown |
|
R4897:Fam186a
|
UTSW |
15 |
99,843,158 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4902:Fam186a
|
UTSW |
15 |
99,844,723 (GRCm39) |
missense |
unknown |
|
R4950:Fam186a
|
UTSW |
15 |
99,839,534 (GRCm39) |
missense |
unknown |
|
R4995:Fam186a
|
UTSW |
15 |
99,842,980 (GRCm39) |
missense |
probably benign |
0.27 |
R5062:Fam186a
|
UTSW |
15 |
99,842,527 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5124:Fam186a
|
UTSW |
15 |
99,840,977 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5133:Fam186a
|
UTSW |
15 |
99,853,374 (GRCm39) |
missense |
unknown |
|
R5424:Fam186a
|
UTSW |
15 |
99,843,644 (GRCm39) |
missense |
unknown |
|
R5624:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5628:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5637:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5639:Fam186a
|
UTSW |
15 |
99,844,931 (GRCm39) |
missense |
unknown |
|
R5652:Fam186a
|
UTSW |
15 |
99,843,253 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5673:Fam186a
|
UTSW |
15 |
99,839,628 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5799:Fam186a
|
UTSW |
15 |
99,864,705 (GRCm39) |
nonsense |
probably null |
|
R5965:Fam186a
|
UTSW |
15 |
99,842,978 (GRCm39) |
missense |
probably benign |
0.37 |
R6044:Fam186a
|
UTSW |
15 |
99,839,878 (GRCm39) |
missense |
probably damaging |
0.97 |
R6077:Fam186a
|
UTSW |
15 |
99,840,584 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6120:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
R6185:Fam186a
|
UTSW |
15 |
99,845,530 (GRCm39) |
missense |
unknown |
|
R6186:Fam186a
|
UTSW |
15 |
99,845,206 (GRCm39) |
missense |
unknown |
|
R6242:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
R6351:Fam186a
|
UTSW |
15 |
99,839,623 (GRCm39) |
missense |
probably damaging |
0.97 |
R6368:Fam186a
|
UTSW |
15 |
99,841,198 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6369:Fam186a
|
UTSW |
15 |
99,845,212 (GRCm39) |
missense |
unknown |
|
R6559:Fam186a
|
UTSW |
15 |
99,842,356 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6855:Fam186a
|
UTSW |
15 |
99,852,756 (GRCm39) |
missense |
unknown |
|
R6867:Fam186a
|
UTSW |
15 |
99,843,731 (GRCm39) |
missense |
unknown |
|
R6957:Fam186a
|
UTSW |
15 |
99,844,357 (GRCm39) |
missense |
unknown |
|
R6961:Fam186a
|
UTSW |
15 |
99,838,082 (GRCm39) |
missense |
probably benign |
0.16 |
R6994:Fam186a
|
UTSW |
15 |
99,840,347 (GRCm39) |
missense |
probably benign |
0.35 |
R6996:Fam186a
|
UTSW |
15 |
99,853,374 (GRCm39) |
missense |
unknown |
|
R7062:Fam186a
|
UTSW |
15 |
99,831,521 (GRCm39) |
unclassified |
probably benign |
|
R7064:Fam186a
|
UTSW |
15 |
99,839,557 (GRCm39) |
missense |
unknown |
|
R7173:Fam186a
|
UTSW |
15 |
99,843,531 (GRCm39) |
missense |
unknown |
|
R7244:Fam186a
|
UTSW |
15 |
99,844,273 (GRCm39) |
missense |
unknown |
|
R7270:Fam186a
|
UTSW |
15 |
99,842,033 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7410:Fam186a
|
UTSW |
15 |
99,844,826 (GRCm39) |
nonsense |
probably null |
|
R7437:Fam186a
|
UTSW |
15 |
99,840,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Fam186a
|
UTSW |
15 |
99,845,395 (GRCm39) |
missense |
unknown |
|
R7487:Fam186a
|
UTSW |
15 |
99,840,017 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7526:Fam186a
|
UTSW |
15 |
99,839,796 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7650:Fam186a
|
UTSW |
15 |
99,837,788 (GRCm39) |
missense |
unknown |
|
R7658:Fam186a
|
UTSW |
15 |
99,837,725 (GRCm39) |
missense |
unknown |
|
R7663:Fam186a
|
UTSW |
15 |
99,842,950 (GRCm39) |
missense |
probably benign |
0.00 |
R7703:Fam186a
|
UTSW |
15 |
99,852,678 (GRCm39) |
missense |
unknown |
|
R7814:Fam186a
|
UTSW |
15 |
99,842,545 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7958:Fam186a
|
UTSW |
15 |
99,841,189 (GRCm39) |
missense |
probably damaging |
0.99 |
R7970:Fam186a
|
UTSW |
15 |
99,831,467 (GRCm39) |
missense |
unknown |
|
R8076:Fam186a
|
UTSW |
15 |
99,841,351 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8087:Fam186a
|
UTSW |
15 |
99,839,725 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8130:Fam186a
|
UTSW |
15 |
99,841,914 (GRCm39) |
frame shift |
probably null |
|
R8239:Fam186a
|
UTSW |
15 |
99,839,191 (GRCm39) |
missense |
unknown |
|
R8246:Fam186a
|
UTSW |
15 |
99,838,428 (GRCm39) |
missense |
unknown |
|
R8446:Fam186a
|
UTSW |
15 |
99,845,335 (GRCm39) |
missense |
unknown |
|
R8469:Fam186a
|
UTSW |
15 |
99,845,186 (GRCm39) |
missense |
unknown |
|
R8790:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8808:Fam186a
|
UTSW |
15 |
99,842,604 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8848:Fam186a
|
UTSW |
15 |
99,838,034 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9083:Fam186a
|
UTSW |
15 |
99,843,079 (GRCm39) |
missense |
probably benign |
0.27 |
R9106:Fam186a
|
UTSW |
15 |
99,844,107 (GRCm39) |
small deletion |
probably benign |
|
R9116:Fam186a
|
UTSW |
15 |
99,840,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9156:Fam186a
|
UTSW |
15 |
99,841,159 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9227:Fam186a
|
UTSW |
15 |
99,853,384 (GRCm39) |
missense |
unknown |
|
R9250:Fam186a
|
UTSW |
15 |
99,845,330 (GRCm39) |
missense |
unknown |
|
R9282:Fam186a
|
UTSW |
15 |
99,839,879 (GRCm39) |
missense |
probably damaging |
0.97 |
R9495:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
R9514:Fam186a
|
UTSW |
15 |
99,844,766 (GRCm39) |
missense |
unknown |
|
R9521:Fam186a
|
UTSW |
15 |
99,841,471 (GRCm39) |
missense |
probably damaging |
0.97 |
R9553:Fam186a
|
UTSW |
15 |
99,844,561 (GRCm39) |
missense |
unknown |
|
R9641:Fam186a
|
UTSW |
15 |
99,838,244 (GRCm39) |
missense |
probably benign |
0.00 |
R9655:Fam186a
|
UTSW |
15 |
99,840,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R9661:Fam186a
|
UTSW |
15 |
99,842,492 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9673:Fam186a
|
UTSW |
15 |
99,841,024 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9762:Fam186a
|
UTSW |
15 |
99,842,393 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0021:Fam186a
|
UTSW |
15 |
99,843,316 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Fam186a
|
UTSW |
15 |
99,843,875 (GRCm39) |
missense |
unknown |
|
|