Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
C |
G |
10: 100,439,390 (GRCm39) |
P187R |
probably damaging |
Het |
Abhd5 |
T |
C |
9: 122,208,079 (GRCm39) |
|
probably null |
Het |
Acadvl |
A |
G |
11: 69,905,617 (GRCm39) |
|
probably null |
Het |
Actn1 |
T |
C |
12: 80,251,852 (GRCm39) |
E75G |
probably damaging |
Het |
Adam4 |
A |
T |
12: 81,467,651 (GRCm39) |
N323K |
possibly damaging |
Het |
Anks6 |
G |
A |
4: 47,027,152 (GRCm39) |
R689W |
probably damaging |
Het |
Anxa2 |
T |
C |
9: 69,392,523 (GRCm39) |
I124T |
probably damaging |
Het |
Aph1c |
T |
C |
9: 66,740,547 (GRCm39) |
T10A |
probably benign |
Het |
Arhgap40 |
T |
A |
2: 158,388,721 (GRCm39) |
W552R |
probably benign |
Het |
Baz2b |
C |
T |
2: 59,778,598 (GRCm39) |
R754H |
possibly damaging |
Het |
Blmh |
A |
G |
11: 76,857,607 (GRCm39) |
Y147C |
probably damaging |
Het |
C1galt1 |
C |
T |
6: 7,866,402 (GRCm39) |
L83F |
probably damaging |
Het |
Ccdc168 |
A |
G |
1: 44,096,130 (GRCm39) |
V1656A |
probably benign |
Het |
Cdh23 |
A |
T |
10: 60,215,122 (GRCm39) |
Y1403N |
possibly damaging |
Het |
Cic |
A |
T |
7: 24,993,235 (GRCm39) |
|
probably null |
Het |
Coro1b |
T |
A |
19: 4,200,583 (GRCm39) |
V200D |
possibly damaging |
Het |
Csl |
T |
A |
10: 99,593,817 (GRCm39) |
E416V |
probably damaging |
Het |
Cyp3a25 |
A |
G |
5: 145,938,257 (GRCm39) |
|
probably null |
Het |
Dennd2d |
T |
A |
3: 106,399,875 (GRCm39) |
F266Y |
probably damaging |
Het |
Dnah10 |
A |
G |
5: 124,838,016 (GRCm39) |
E1072G |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,026,031 (GRCm39) |
K3435N |
probably damaging |
Het |
Dnah9 |
G |
A |
11: 65,772,587 (GRCm39) |
A3715V |
probably damaging |
Het |
Fam186a |
G |
A |
15: 99,845,536 (GRCm39) |
S236L |
unknown |
Het |
Frs3 |
A |
G |
17: 48,013,903 (GRCm39) |
T199A |
probably benign |
Het |
Fsd1 |
A |
G |
17: 56,300,870 (GRCm39) |
N243S |
probably benign |
Het |
Gabra5 |
A |
C |
7: 57,058,641 (GRCm39) |
L369R |
probably benign |
Het |
Gask1b |
A |
G |
3: 79,848,771 (GRCm39) |
N506D |
possibly damaging |
Het |
Gins4 |
A |
G |
8: 23,724,792 (GRCm39) |
V54A |
probably benign |
Het |
Gli1 |
T |
C |
10: 127,170,138 (GRCm39) |
E339G |
possibly damaging |
Het |
Gpr83 |
T |
A |
9: 14,779,493 (GRCm39) |
C182S |
probably null |
Het |
Gspt1 |
A |
G |
16: 11,038,719 (GRCm39) |
V627A |
probably damaging |
Het |
Heatr1 |
T |
C |
13: 12,427,040 (GRCm39) |
C722R |
probably benign |
Het |
Jak1 |
C |
T |
4: 101,020,119 (GRCm39) |
R680Q |
probably damaging |
Het |
Kif2c |
A |
G |
4: 117,027,137 (GRCm39) |
V287A |
probably damaging |
Het |
Kmo |
C |
T |
1: 175,479,184 (GRCm39) |
P240L |
possibly damaging |
Het |
Kmo |
A |
G |
1: 175,484,368 (GRCm39) |
E366G |
probably damaging |
Het |
Lepr |
A |
T |
4: 101,646,541 (GRCm39) |
N824I |
probably damaging |
Het |
Lyrm7 |
T |
A |
11: 54,739,425 (GRCm39) |
H75L |
possibly damaging |
Het |
Map4k1 |
A |
T |
7: 28,690,461 (GRCm39) |
Q351L |
probably benign |
Het |
Matcap2 |
T |
G |
9: 22,341,671 (GRCm39) |
L114R |
probably benign |
Het |
Mgam |
T |
C |
6: 40,638,617 (GRCm39) |
I450T |
probably benign |
Het |
Nbeal2 |
A |
G |
9: 110,465,373 (GRCm39) |
L955P |
probably damaging |
Het |
Nlrp9c |
T |
C |
7: 26,077,526 (GRCm39) |
K752R |
possibly damaging |
Het |
Nsmaf |
A |
T |
4: 6,438,062 (GRCm39) |
I70K |
probably benign |
Het |
Or14a257 |
A |
G |
7: 86,138,333 (GRCm39) |
M142T |
probably damaging |
Het |
Or5ac19 |
C |
T |
16: 59,089,307 (GRCm39) |
C241Y |
probably damaging |
Het |
Otud7a |
A |
G |
7: 63,408,391 (GRCm39) |
Y898C |
probably damaging |
Het |
Pcdhb18 |
A |
C |
18: 37,623,945 (GRCm39) |
D425A |
probably damaging |
Het |
Prdm1 |
A |
T |
10: 44,315,982 (GRCm39) |
L733* |
probably null |
Het |
Prdm2 |
A |
T |
4: 142,862,153 (GRCm39) |
I379N |
probably damaging |
Het |
Ptprg |
A |
T |
14: 12,220,596 (GRCm38) |
Y436F |
probably damaging |
Het |
Riok3 |
A |
G |
18: 12,270,363 (GRCm39) |
D167G |
probably damaging |
Het |
Rnf215 |
G |
T |
11: 4,085,451 (GRCm39) |
R60L |
probably damaging |
Het |
Scart1 |
G |
A |
7: 139,808,069 (GRCm39) |
V747I |
probably benign |
Het |
Sdk1 |
A |
T |
5: 141,985,705 (GRCm39) |
H779L |
probably benign |
Het |
Serpine2 |
A |
G |
1: 79,772,748 (GRCm39) |
F390L |
probably damaging |
Het |
Sh3d21 |
T |
A |
4: 126,045,519 (GRCm39) |
K387* |
probably null |
Het |
Slc13a2 |
T |
C |
11: 78,288,572 (GRCm39) |
Y568C |
possibly damaging |
Het |
Slc27a5 |
T |
C |
7: 12,722,386 (GRCm39) |
|
probably null |
Het |
Slc32a1 |
T |
C |
2: 158,456,497 (GRCm39) |
L384P |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,241,025 (GRCm39) |
N454D |
probably benign |
Het |
Spag8 |
T |
C |
4: 43,652,777 (GRCm39) |
Y228C |
possibly damaging |
Het |
Spata31e4 |
G |
A |
13: 50,854,443 (GRCm39) |
|
probably null |
Het |
Spc25 |
T |
C |
2: 69,030,431 (GRCm39) |
I71V |
probably damaging |
Het |
Tcte1 |
T |
A |
17: 45,846,178 (GRCm39) |
F261I |
probably damaging |
Het |
Thsd7a |
T |
A |
6: 12,471,174 (GRCm39) |
K481N |
probably benign |
Het |
Tll2 |
G |
T |
19: 41,074,839 (GRCm39) |
N908K |
probably benign |
Het |
Tmem236 |
T |
C |
2: 14,197,091 (GRCm39) |
V93A |
probably benign |
Het |
Top2b |
G |
A |
14: 16,408,953 (GRCm38) |
|
probably null |
Het |
Topaz1 |
G |
A |
9: 122,596,076 (GRCm39) |
S949N |
probably benign |
Het |
Triobp |
A |
G |
15: 78,857,938 (GRCm39) |
T1180A |
probably benign |
Het |
Trip11 |
A |
C |
12: 101,852,419 (GRCm39) |
D548E |
probably benign |
Het |
Trpv2 |
T |
A |
11: 62,480,652 (GRCm39) |
|
probably null |
Het |
Ulbp3 |
A |
G |
10: 3,075,230 (GRCm39) |
|
noncoding transcript |
Het |
Vmn1r12 |
T |
A |
6: 57,136,540 (GRCm39) |
H212Q |
probably damaging |
Het |
Vmn2r112 |
A |
G |
17: 22,837,884 (GRCm39) |
T782A |
possibly damaging |
Het |
Vmn2r7 |
A |
G |
3: 64,623,876 (GRCm39) |
V239A |
possibly damaging |
Het |
Vmn2r80 |
T |
A |
10: 79,030,053 (GRCm39) |
N626K |
probably damaging |
Het |
Vmn2r99 |
A |
G |
17: 19,600,322 (GRCm39) |
S449G |
probably benign |
Het |
Wfikkn2 |
T |
C |
11: 94,128,933 (GRCm39) |
T403A |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,346,023 (GRCm39) |
I2755V |
probably benign |
Het |
Yjefn3 |
A |
G |
8: 70,341,729 (GRCm39) |
V153A |
probably benign |
Het |
Zfp677 |
C |
A |
17: 21,617,499 (GRCm39) |
H185Q |
possibly damaging |
Het |
Zfp947 |
C |
T |
17: 22,365,273 (GRCm39) |
V134I |
probably benign |
Het |
|
Other mutations in Gm12185 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00433:Gm12185
|
APN |
11 |
48,798,049 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00495:Gm12185
|
APN |
11 |
48,798,688 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01763:Gm12185
|
APN |
11 |
48,806,671 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01919:Gm12185
|
APN |
11 |
48,798,886 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03388:Gm12185
|
APN |
11 |
48,799,113 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03404:Gm12185
|
APN |
11 |
48,798,864 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4458001:Gm12185
|
UTSW |
11 |
48,798,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R0347:Gm12185
|
UTSW |
11 |
48,806,009 (GRCm39) |
missense |
probably benign |
0.29 |
R0488:Gm12185
|
UTSW |
11 |
48,798,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1168:Gm12185
|
UTSW |
11 |
48,806,182 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1223:Gm12185
|
UTSW |
11 |
48,798,103 (GRCm39) |
missense |
probably damaging |
0.98 |
R1417:Gm12185
|
UTSW |
11 |
48,798,669 (GRCm39) |
missense |
probably damaging |
1.00 |
R1468:Gm12185
|
UTSW |
11 |
48,806,501 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1468:Gm12185
|
UTSW |
11 |
48,806,501 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1558:Gm12185
|
UTSW |
11 |
48,806,262 (GRCm39) |
missense |
probably damaging |
0.99 |
R1630:Gm12185
|
UTSW |
11 |
48,798,717 (GRCm39) |
missense |
probably benign |
0.31 |
R1758:Gm12185
|
UTSW |
11 |
48,798,859 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1793:Gm12185
|
UTSW |
11 |
48,806,583 (GRCm39) |
nonsense |
probably null |
|
R1908:Gm12185
|
UTSW |
11 |
48,806,231 (GRCm39) |
missense |
probably benign |
0.00 |
R1983:Gm12185
|
UTSW |
11 |
48,806,183 (GRCm39) |
missense |
probably benign |
0.01 |
R3917:Gm12185
|
UTSW |
11 |
48,806,760 (GRCm39) |
missense |
probably benign |
0.01 |
R3969:Gm12185
|
UTSW |
11 |
48,798,172 (GRCm39) |
missense |
probably benign |
0.03 |
R3970:Gm12185
|
UTSW |
11 |
48,798,172 (GRCm39) |
missense |
probably benign |
0.03 |
R4510:Gm12185
|
UTSW |
11 |
48,799,305 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4511:Gm12185
|
UTSW |
11 |
48,799,305 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4529:Gm12185
|
UTSW |
11 |
48,798,921 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4529:Gm12185
|
UTSW |
11 |
48,798,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4532:Gm12185
|
UTSW |
11 |
48,798,921 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4532:Gm12185
|
UTSW |
11 |
48,798,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4533:Gm12185
|
UTSW |
11 |
48,798,921 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4533:Gm12185
|
UTSW |
11 |
48,798,747 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Gm12185
|
UTSW |
11 |
48,806,367 (GRCm39) |
missense |
probably benign |
0.05 |
R5094:Gm12185
|
UTSW |
11 |
48,798,375 (GRCm39) |
missense |
probably benign |
0.35 |
R5238:Gm12185
|
UTSW |
11 |
48,799,044 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5306:Gm12185
|
UTSW |
11 |
48,806,382 (GRCm39) |
missense |
probably benign |
0.03 |
R5371:Gm12185
|
UTSW |
11 |
48,806,566 (GRCm39) |
missense |
probably benign |
0.01 |
R5995:Gm12185
|
UTSW |
11 |
48,806,540 (GRCm39) |
missense |
probably benign |
0.40 |
R6113:Gm12185
|
UTSW |
11 |
48,806,167 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6147:Gm12185
|
UTSW |
11 |
48,806,717 (GRCm39) |
missense |
probably benign |
|
R6160:Gm12185
|
UTSW |
11 |
48,799,255 (GRCm39) |
nonsense |
probably null |
|
R6247:Gm12185
|
UTSW |
11 |
48,806,735 (GRCm39) |
missense |
probably damaging |
0.98 |
R6264:Gm12185
|
UTSW |
11 |
48,807,002 (GRCm39) |
missense |
probably benign |
0.01 |
R6748:Gm12185
|
UTSW |
11 |
48,807,123 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6765:Gm12185
|
UTSW |
11 |
48,806,531 (GRCm39) |
missense |
probably benign |
0.12 |
R6970:Gm12185
|
UTSW |
11 |
48,798,739 (GRCm39) |
nonsense |
probably null |
|
R7028:Gm12185
|
UTSW |
11 |
48,799,071 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7033:Gm12185
|
UTSW |
11 |
48,806,826 (GRCm39) |
missense |
probably benign |
|
R7512:Gm12185
|
UTSW |
11 |
48,806,717 (GRCm39) |
missense |
probably benign |
|
R7609:Gm12185
|
UTSW |
11 |
48,806,850 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7673:Gm12185
|
UTSW |
11 |
48,798,455 (GRCm39) |
missense |
probably benign |
0.45 |
R8848:Gm12185
|
UTSW |
11 |
48,806,280 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9578:Gm12185
|
UTSW |
11 |
48,806,408 (GRCm39) |
missense |
probably benign |
|
R9580:Gm12185
|
UTSW |
11 |
48,799,192 (GRCm39) |
missense |
possibly damaging |
0.48 |
R9712:Gm12185
|
UTSW |
11 |
48,798,216 (GRCm39) |
missense |
probably benign |
0.03 |
R9760:Gm12185
|
UTSW |
11 |
48,806,168 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Gm12185
|
UTSW |
11 |
48,798,913 (GRCm39) |
missense |
probably benign |
0.21 |
Z1177:Gm12185
|
UTSW |
11 |
48,807,129 (GRCm39) |
missense |
probably benign |
|
|