Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
T |
C |
11: 58,316,593 (GRCm39) |
I191T |
probably damaging |
Het |
2310003L06Rik |
T |
C |
5: 88,120,671 (GRCm39) |
L476P |
possibly damaging |
Het |
Aasdh |
T |
C |
5: 77,035,924 (GRCm39) |
D387G |
probably damaging |
Het |
Ahsa2 |
T |
A |
11: 23,440,415 (GRCm39) |
T327S |
probably benign |
Het |
Ap3d1 |
A |
T |
10: 80,553,678 (GRCm39) |
V523E |
probably damaging |
Het |
Baz2b |
C |
A |
2: 59,747,769 (GRCm39) |
R1298L |
probably damaging |
Het |
Cacna2d3 |
T |
C |
14: 28,765,503 (GRCm39) |
T802A |
possibly damaging |
Het |
Cdh23 |
G |
T |
10: 60,173,043 (GRCm39) |
T1714K |
probably damaging |
Het |
Chrna3 |
A |
T |
9: 54,923,408 (GRCm39) |
D133E |
probably benign |
Het |
Cnot1 |
C |
T |
8: 96,486,726 (GRCm39) |
|
probably null |
Het |
Col16a1 |
A |
T |
4: 129,990,295 (GRCm39) |
N1396Y |
unknown |
Het |
Cox11 |
A |
G |
11: 90,529,245 (GRCm39) |
N77S |
probably benign |
Het |
Ctsf |
T |
G |
19: 4,906,567 (GRCm39) |
F165V |
probably damaging |
Het |
Cytip |
A |
G |
2: 58,037,920 (GRCm39) |
V148A |
probably damaging |
Het |
Diaph1 |
T |
C |
18: 38,023,862 (GRCm39) |
I659V |
unknown |
Het |
Dmxl2 |
A |
T |
9: 54,368,370 (GRCm39) |
M26K |
probably benign |
Het |
Erp44 |
T |
A |
4: 48,196,904 (GRCm39) |
I340F |
probably benign |
Het |
Frem2 |
C |
T |
3: 53,429,589 (GRCm39) |
V2793I |
probably benign |
Het |
Gm19410 |
A |
G |
8: 36,266,539 (GRCm39) |
E1064G |
probably damaging |
Het |
Gria4 |
T |
C |
9: 4,503,588 (GRCm39) |
I343V |
probably benign |
Het |
Grsf1 |
T |
A |
5: 88,819,150 (GRCm39) |
N228Y |
probably damaging |
Het |
H3c13 |
C |
A |
3: 96,176,309 (GRCm39) |
Y100* |
probably null |
Het |
Ighv1-18 |
A |
T |
12: 114,646,381 (GRCm39) |
N74K |
probably benign |
Het |
Kcnh6 |
A |
T |
11: 105,914,703 (GRCm39) |
T703S |
probably benign |
Het |
Lrp1b |
T |
A |
2: 41,000,798 (GRCm39) |
D2256V |
|
Het |
Lrrc63 |
T |
C |
14: 75,360,447 (GRCm39) |
T352A |
possibly damaging |
Het |
Lztfl1 |
T |
C |
9: 123,531,194 (GRCm39) |
E258G |
probably damaging |
Het |
Mcph1 |
T |
C |
8: 18,721,122 (GRCm39) |
I650T |
possibly damaging |
Het |
Mep1a |
T |
C |
17: 43,788,997 (GRCm39) |
D606G |
possibly damaging |
Het |
Muc16 |
T |
C |
9: 18,516,578 (GRCm39) |
I313M |
|
Het |
Myh7b |
A |
G |
2: 155,462,356 (GRCm39) |
Y353C |
probably null |
Het |
Nfatc1 |
A |
G |
18: 80,725,504 (GRCm39) |
L420P |
probably damaging |
Het |
Olfml1 |
A |
G |
7: 107,170,392 (GRCm39) |
E93G |
probably damaging |
Het |
Or6b1 |
A |
T |
6: 42,814,938 (GRCm39) |
E41V |
probably damaging |
Het |
Or8c11 |
A |
G |
9: 38,289,357 (GRCm39) |
H54R |
probably benign |
Het |
Pax1 |
A |
T |
2: 147,208,034 (GRCm39) |
N214I |
probably damaging |
Het |
Pcdhb17 |
C |
A |
18: 37,619,801 (GRCm39) |
H530Q |
probably benign |
Het |
Pcdhgb7 |
A |
T |
18: 37,885,321 (GRCm39) |
M164L |
probably benign |
Het |
Pcolce |
T |
C |
5: 137,603,474 (GRCm39) |
N453S |
probably benign |
Het |
Prr36 |
T |
C |
8: 4,262,982 (GRCm39) |
T895A |
probably benign |
Het |
Ptprq |
C |
T |
10: 107,480,007 (GRCm39) |
V1088I |
probably benign |
Het |
Rab5a |
T |
A |
17: 53,807,485 (GRCm39) |
F174I |
probably damaging |
Het |
Rapgef4 |
A |
G |
2: 72,010,315 (GRCm39) |
D291G |
probably benign |
Het |
Rbm25 |
A |
T |
12: 83,721,864 (GRCm39) |
K683N |
possibly damaging |
Het |
Rbpj |
T |
C |
5: 53,803,240 (GRCm39) |
I156T |
probably damaging |
Het |
Rgsl1 |
A |
G |
1: 153,669,610 (GRCm39) |
S259P |
possibly damaging |
Het |
Ring1 |
T |
C |
17: 34,242,109 (GRCm39) |
D100G |
probably damaging |
Het |
Ryr3 |
A |
T |
2: 112,690,110 (GRCm39) |
D1166E |
probably damaging |
Het |
Sacs |
A |
G |
14: 61,443,539 (GRCm39) |
K1862E |
possibly damaging |
Het |
Scamp5 |
A |
G |
9: 57,354,465 (GRCm39) |
I63T |
possibly damaging |
Het |
Septin14 |
C |
T |
5: 129,763,092 (GRCm39) |
A334T |
possibly damaging |
Het |
Sh3rf2 |
A |
T |
18: 42,289,201 (GRCm39) |
Q706L |
probably benign |
Het |
Skap2 |
A |
T |
6: 51,884,934 (GRCm39) |
H242Q |
probably benign |
Het |
Spmap2l |
T |
C |
5: 77,164,444 (GRCm39) |
I149T |
probably benign |
Het |
Tfpt |
A |
G |
7: 3,623,744 (GRCm39) |
|
probably null |
Het |
Thg1l |
T |
G |
11: 45,846,120 (GRCm39) |
D58A |
probably damaging |
Het |
Thyn1 |
A |
G |
9: 26,918,143 (GRCm39) |
E177G |
probably benign |
Het |
Tmem151b |
C |
T |
17: 45,856,724 (GRCm39) |
A239T |
probably damaging |
Het |
Ttc21a |
T |
C |
9: 119,788,095 (GRCm39) |
V840A |
probably benign |
Het |
Usp32 |
A |
T |
11: 84,968,153 (GRCm39) |
V170E |
probably damaging |
Het |
Vmn2r29 |
A |
G |
7: 7,234,864 (GRCm39) |
V674A |
probably benign |
Het |
Vwa8 |
A |
G |
14: 79,263,513 (GRCm39) |
N781S |
probably damaging |
Het |
Zbtb7c |
C |
A |
18: 76,270,433 (GRCm39) |
Q174K |
probably benign |
Het |
Zeb1 |
T |
C |
18: 5,766,917 (GRCm39) |
I476T |
probably benign |
Het |
Zfp91 |
A |
T |
19: 12,754,241 (GRCm39) |
D282E |
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 |
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 |
|
R8676:Fam186a
|
UTSW |
15 |
99,845,023 (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 |
|
|