Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ak1 |
A |
T |
2: 32,521,189 (GRCm39) |
E119D |
probably benign |
Het |
Alox5 |
A |
T |
6: 116,390,811 (GRCm39) |
|
probably null |
Het |
Atad5 |
T |
C |
11: 80,011,515 (GRCm39) |
V1294A |
probably damaging |
Het |
BB019430 |
A |
G |
10: 58,539,865 (GRCm39) |
|
noncoding transcript |
Het |
Bbs9 |
T |
C |
9: 22,490,011 (GRCm39) |
F261L |
probably benign |
Het |
Catsperb |
A |
T |
12: 101,554,244 (GRCm39) |
N646I |
possibly damaging |
Het |
Ccdc112 |
A |
G |
18: 46,429,356 (GRCm39) |
I114T |
probably damaging |
Het |
Cecr2 |
T |
C |
6: 120,727,877 (GRCm39) |
L340P |
probably damaging |
Het |
Ces2e |
T |
A |
8: 105,653,817 (GRCm39) |
V85E |
probably damaging |
Het |
Cnpy2 |
C |
A |
10: 128,161,964 (GRCm39) |
T79K |
probably damaging |
Het |
Cntn4 |
G |
A |
6: 106,414,874 (GRCm39) |
R135H |
possibly damaging |
Het |
Cyp3a16 |
C |
A |
5: 145,389,659 (GRCm39) |
M235I |
probably benign |
Het |
Dll3 |
A |
G |
7: 27,995,860 (GRCm39) |
C314R |
probably damaging |
Het |
Dnah7c |
A |
G |
1: 46,728,085 (GRCm39) |
N2928D |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Dqx1 |
C |
A |
6: 83,037,993 (GRCm39) |
D460E |
probably benign |
Het |
Dync1h1 |
C |
A |
12: 110,624,560 (GRCm39) |
T3700N |
probably damaging |
Het |
Ehbp1 |
A |
G |
11: 22,051,164 (GRCm39) |
C438R |
probably damaging |
Het |
Ehd3 |
T |
G |
17: 74,112,299 (GRCm39) |
V21G |
probably damaging |
Het |
Ero1b |
G |
A |
13: 12,619,325 (GRCm39) |
V440I |
probably damaging |
Het |
Fpgt |
G |
A |
3: 154,793,550 (GRCm39) |
A159V |
probably damaging |
Het |
Gcn1 |
T |
C |
5: 115,714,229 (GRCm39) |
L123P |
possibly damaging |
Het |
Gm14496 |
A |
T |
2: 181,639,226 (GRCm39) |
R439W |
probably damaging |
Het |
Gm4353 |
G |
C |
7: 115,683,648 (GRCm39) |
P49R |
probably damaging |
Het |
Gsdmc2 |
C |
T |
15: 63,700,101 (GRCm39) |
A224T |
probably benign |
Het |
Hnf1a |
T |
C |
5: 115,108,732 (GRCm39) |
T58A |
probably benign |
Het |
Igkv4-80 |
A |
C |
6: 68,993,649 (GRCm39) |
S81A |
probably benign |
Het |
Kcns1 |
T |
C |
2: 164,010,021 (GRCm39) |
Y246C |
probably damaging |
Het |
Kif26b |
A |
G |
1: 178,742,892 (GRCm39) |
E549G |
probably benign |
Het |
Krt9 |
T |
C |
11: 100,080,863 (GRCm39) |
I330V |
probably benign |
Het |
Lair1 |
A |
T |
7: 4,032,033 (GRCm39) |
S25T |
probably benign |
Het |
Lhx4 |
T |
C |
1: 155,581,013 (GRCm39) |
T171A |
possibly damaging |
Het |
Luzp2 |
A |
G |
7: 54,816,996 (GRCm39) |
I149V |
possibly damaging |
Het |
Mcoln1 |
T |
A |
8: 3,557,422 (GRCm39) |
S143T |
probably benign |
Het |
Mcph1 |
A |
G |
8: 18,675,574 (GRCm39) |
|
probably null |
Het |
Mgat5 |
G |
A |
1: 127,396,986 (GRCm39) |
V578M |
probably damaging |
Het |
Mis18bp1 |
G |
A |
12: 65,208,209 (GRCm39) |
T168M |
probably benign |
Het |
Mroh2a |
G |
T |
1: 88,182,657 (GRCm39) |
R1195L |
possibly damaging |
Het |
Myom1 |
T |
C |
17: 71,379,114 (GRCm39) |
V626A |
probably damaging |
Het |
Naa80 |
C |
T |
9: 107,460,818 (GRCm39) |
R238C |
probably damaging |
Het |
Ncam1 |
T |
C |
9: 49,418,921 (GRCm39) |
|
probably benign |
Het |
Nlrp2 |
A |
T |
7: 5,301,858 (GRCm39) |
F211L |
probably benign |
Het |
Or10a49 |
A |
T |
7: 108,467,993 (GRCm39) |
F123I |
probably damaging |
Het |
Or10q12 |
T |
A |
19: 13,746,126 (GRCm39) |
M140K |
probably damaging |
Het |
Or2ad1 |
T |
A |
13: 21,326,450 (GRCm39) |
Y259F |
probably damaging |
Het |
Osbpl11 |
G |
A |
16: 33,054,863 (GRCm39) |
V649I |
probably benign |
Het |
Oscar |
A |
T |
7: 3,619,016 (GRCm39) |
|
probably null |
Het |
Pax8 |
T |
A |
2: 24,331,652 (GRCm39) |
M144L |
probably benign |
Het |
Pcnt |
T |
C |
10: 76,205,688 (GRCm39) |
T2555A |
probably benign |
Het |
Plpp2 |
G |
A |
10: 79,366,763 (GRCm39) |
T51M |
probably damaging |
Het |
Pnkp |
C |
T |
7: 44,511,827 (GRCm39) |
S113L |
probably damaging |
Het |
Prl7c1 |
T |
C |
13: 27,957,742 (GRCm39) |
M233V |
probably benign |
Het |
Prox1 |
A |
C |
1: 189,894,319 (GRCm39) |
F42C |
probably damaging |
Het |
Pwwp2b |
A |
T |
7: 138,835,978 (GRCm39) |
Q473L |
possibly damaging |
Het |
Rims4 |
A |
T |
2: 163,707,443 (GRCm39) |
N127K |
probably null |
Het |
Scn1a |
T |
C |
2: 66,158,820 (GRCm39) |
T367A |
possibly damaging |
Het |
Slc23a2 |
A |
G |
2: 131,898,800 (GRCm39) |
I579T |
possibly damaging |
Het |
Sp9 |
T |
C |
2: 73,103,962 (GRCm39) |
V172A |
possibly damaging |
Het |
Spta1 |
T |
A |
1: 174,003,396 (GRCm39) |
L109Q |
probably damaging |
Het |
Synj2 |
A |
T |
17: 6,038,343 (GRCm39) |
|
probably benign |
Het |
Tcstv2c |
T |
C |
13: 120,616,206 (GRCm39) |
V15A |
probably damaging |
Het |
Tnrc18 |
A |
T |
5: 142,750,932 (GRCm39) |
M1216K |
unknown |
Het |
Tpst2 |
T |
A |
5: 112,457,687 (GRCm39) |
Y69* |
probably null |
Het |
Tpx2 |
C |
A |
2: 152,735,535 (GRCm39) |
A721E |
probably benign |
Het |
Trmt1l |
A |
G |
1: 151,330,755 (GRCm39) |
T591A |
probably benign |
Het |
Tubgcp4 |
T |
A |
2: 121,015,330 (GRCm39) |
|
probably benign |
Het |
Ubiad1 |
T |
C |
4: 148,528,556 (GRCm39) |
T118A |
possibly damaging |
Het |
Unc13c |
T |
C |
9: 73,424,566 (GRCm39) |
T2017A |
probably damaging |
Het |
Vmn1r59 |
G |
T |
7: 5,457,108 (GRCm39) |
N217K |
probably benign |
Het |
Vmn2r87 |
T |
C |
10: 130,308,367 (GRCm39) |
I624V |
probably damaging |
Het |
Wdr4 |
A |
G |
17: 31,718,129 (GRCm39) |
V315A |
probably benign |
Het |
Xpo7 |
T |
C |
14: 70,914,256 (GRCm39) |
|
probably null |
Het |
Zfp827 |
T |
A |
8: 79,787,403 (GRCm39) |
W190R |
probably damaging |
Het |
Zfp971 |
A |
G |
2: 177,674,940 (GRCm39) |
T180A |
probably benign |
Het |
Zfp980 |
G |
A |
4: 145,428,653 (GRCm39) |
G461S |
probably benign |
Het |
|
Other mutations in Plat |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01457:Plat
|
APN |
8 |
23,266,844 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01918:Plat
|
APN |
8 |
23,270,453 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01998:Plat
|
APN |
8 |
23,257,163 (GRCm39) |
missense |
probably benign |
0.31 |
IGL02978:Plat
|
APN |
8 |
23,266,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R0829:Plat
|
UTSW |
8 |
23,262,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R1065:Plat
|
UTSW |
8 |
23,266,879 (GRCm39) |
missense |
probably damaging |
0.99 |
R2316:Plat
|
UTSW |
8 |
23,266,881 (GRCm39) |
missense |
probably benign |
0.04 |
R4485:Plat
|
UTSW |
8 |
23,262,228 (GRCm39) |
missense |
probably benign |
0.01 |
R4875:Plat
|
UTSW |
8 |
23,258,466 (GRCm39) |
missense |
probably benign |
0.03 |
R4924:Plat
|
UTSW |
8 |
23,268,269 (GRCm39) |
missense |
probably damaging |
1.00 |
R5051:Plat
|
UTSW |
8 |
23,263,688 (GRCm39) |
missense |
probably benign |
0.01 |
R5062:Plat
|
UTSW |
8 |
23,262,327 (GRCm39) |
missense |
probably benign |
0.19 |
R5402:Plat
|
UTSW |
8 |
23,262,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R5672:Plat
|
UTSW |
8 |
23,263,664 (GRCm39) |
missense |
probably benign |
0.40 |
R6306:Plat
|
UTSW |
8 |
23,262,282 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7035:Plat
|
UTSW |
8 |
23,262,327 (GRCm39) |
missense |
probably benign |
0.32 |
R7154:Plat
|
UTSW |
8 |
23,268,521 (GRCm39) |
missense |
possibly damaging |
0.76 |
R7297:Plat
|
UTSW |
8 |
23,265,713 (GRCm39) |
missense |
probably benign |
0.12 |
R7432:Plat
|
UTSW |
8 |
23,263,667 (GRCm39) |
missense |
probably damaging |
0.99 |
R7514:Plat
|
UTSW |
8 |
23,265,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R7679:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7680:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7834:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7885:Plat
|
UTSW |
8 |
23,261,736 (GRCm39) |
missense |
probably benign |
0.00 |
R7918:Plat
|
UTSW |
8 |
23,263,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R8039:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8040:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8243:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8347:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8355:Plat
|
UTSW |
8 |
23,261,758 (GRCm39) |
nonsense |
probably null |
|
R8422:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8423:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8424:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8426:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8427:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8485:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8510:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8714:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R8717:Plat
|
UTSW |
8 |
23,262,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R9140:Plat
|
UTSW |
8 |
23,270,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R9148:Plat
|
UTSW |
8 |
23,268,466 (GRCm39) |
missense |
probably damaging |
0.99 |
R9289:Plat
|
UTSW |
8 |
23,272,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R9328:Plat
|
UTSW |
8 |
23,268,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R9378:Plat
|
UTSW |
8 |
23,265,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R9557:Plat
|
UTSW |
8 |
23,262,669 (GRCm39) |
missense |
probably benign |
0.01 |
|