Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadac |
C |
T |
3: 59,947,424 (GRCm39) |
T374M |
probably benign |
Het |
Aspg |
A |
G |
12: 112,087,378 (GRCm39) |
D278G |
possibly damaging |
Het |
Aspm |
C |
A |
1: 139,408,223 (GRCm39) |
A2370E |
probably damaging |
Het |
Ccnt2 |
T |
C |
1: 127,702,873 (GRCm39) |
M65T |
probably damaging |
Het |
Cd163 |
A |
G |
6: 124,294,945 (GRCm39) |
T670A |
probably benign |
Het |
Cpne3 |
G |
A |
4: 19,533,098 (GRCm39) |
T279I |
probably benign |
Het |
Ctdspl |
G |
A |
9: 118,869,598 (GRCm39) |
V227M |
probably damaging |
Het |
Ctnnd2 |
A |
G |
15: 30,619,376 (GRCm39) |
E99G |
probably damaging |
Het |
Dapk1 |
T |
C |
13: 60,896,095 (GRCm39) |
S728P |
probably damaging |
Het |
Dmxl2 |
A |
G |
9: 54,358,163 (GRCm39) |
I512T |
possibly damaging |
Het |
Dop1a |
A |
T |
9: 86,403,695 (GRCm39) |
T1630S |
possibly damaging |
Het |
Dqx1 |
A |
G |
6: 83,037,992 (GRCm39) |
D460G |
probably damaging |
Het |
Foxg1 |
T |
C |
12: 49,431,567 (GRCm39) |
|
probably benign |
Het |
H2-Q2 |
T |
A |
17: 35,564,623 (GRCm39) |
|
probably null |
Het |
Hes6 |
T |
C |
1: 91,340,810 (GRCm39) |
E17G |
possibly damaging |
Het |
Ighv1-42 |
T |
C |
12: 114,900,848 (GRCm39) |
Y79C |
possibly damaging |
Het |
Itfg2 |
T |
C |
6: 128,388,554 (GRCm39) |
D311G |
probably damaging |
Het |
Itgb5 |
T |
A |
16: 33,740,356 (GRCm39) |
C489S |
probably damaging |
Het |
Map4k5 |
A |
T |
12: 69,869,622 (GRCm39) |
C488S |
probably damaging |
Het |
Mark1 |
C |
T |
1: 184,644,825 (GRCm39) |
G377D |
possibly damaging |
Het |
Mat2a |
A |
G |
6: 72,412,096 (GRCm39) |
V318A |
probably damaging |
Het |
Mpp7 |
T |
G |
18: 7,355,049 (GRCm39) |
N459T |
possibly damaging |
Het |
Mrc2 |
C |
A |
11: 105,239,461 (GRCm39) |
N1348K |
probably damaging |
Het |
Mtor |
A |
G |
4: 148,608,930 (GRCm39) |
M1529V |
possibly damaging |
Het |
Mtrr |
C |
T |
13: 68,718,122 (GRCm39) |
|
probably null |
Het |
Nwd1 |
C |
T |
8: 73,394,288 (GRCm39) |
P517L |
probably damaging |
Het |
Or4a27 |
T |
A |
2: 88,559,528 (GRCm39) |
R138S |
probably benign |
Het |
Or8h10 |
A |
G |
2: 86,808,577 (GRCm39) |
S188P |
probably damaging |
Het |
Polr1c |
A |
G |
17: 46,557,095 (GRCm39) |
F63L |
probably damaging |
Het |
Polrmt |
C |
T |
10: 79,582,400 (GRCm39) |
|
probably null |
Het |
Pomt2 |
T |
C |
12: 87,177,125 (GRCm39) |
I287M |
probably damaging |
Het |
Prkar2a |
T |
A |
9: 108,610,342 (GRCm39) |
N190K |
possibly damaging |
Het |
Prl3d3 |
T |
A |
13: 27,341,545 (GRCm39) |
Y59N |
possibly damaging |
Het |
Prl5a1 |
T |
A |
13: 28,335,189 (GRCm39) |
F199L |
probably benign |
Het |
Prpf38b |
A |
G |
3: 108,818,640 (GRCm39) |
V40A |
probably benign |
Het |
Ptchd1 |
T |
A |
X: 154,357,708 (GRCm39) |
Y499F |
probably damaging |
Het |
Ptgs1 |
A |
G |
2: 36,141,311 (GRCm39) |
D586G |
probably benign |
Het |
Slx4 |
T |
C |
16: 3,802,879 (GRCm39) |
K1312E |
probably damaging |
Het |
Smok3c |
A |
G |
5: 138,062,987 (GRCm39) |
D158G |
probably benign |
Het |
Spen |
A |
T |
4: 141,205,374 (GRCm39) |
D1084E |
unknown |
Het |
Tcp11l1 |
C |
T |
2: 104,536,784 (GRCm39) |
G27D |
probably benign |
Het |
Tep1 |
A |
G |
14: 51,076,094 (GRCm39) |
S1679P |
possibly damaging |
Het |
Tmem259 |
C |
T |
10: 79,814,391 (GRCm39) |
V322I |
possibly damaging |
Het |
Tmpo |
A |
T |
10: 90,988,359 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
A |
2: 76,555,137 (GRCm39) |
A30623S |
probably damaging |
Het |
Ube2l3 |
G |
A |
16: 16,977,841 (GRCm39) |
|
probably benign |
Het |
Unkl |
A |
G |
17: 25,418,890 (GRCm39) |
D146G |
probably damaging |
Het |
Vmn1r51 |
A |
T |
6: 90,106,186 (GRCm39) |
H34L |
possibly damaging |
Het |
Vmn2r17 |
A |
G |
5: 109,576,265 (GRCm39) |
T379A |
possibly damaging |
Het |
Zfp35 |
G |
T |
18: 24,136,927 (GRCm39) |
G424C |
probably benign |
Het |
Zfp420 |
T |
A |
7: 29,575,446 (GRCm39) |
H555Q |
probably damaging |
Het |
|
Other mutations in Mroh5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00420:Mroh5
|
APN |
15 |
73,664,638 (GRCm39) |
splice site |
probably benign |
|
IGL00466:Mroh5
|
APN |
15 |
73,664,638 (GRCm39) |
splice site |
probably benign |
|
IGL02937:Mroh5
|
APN |
15 |
73,661,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R0102:Mroh5
|
UTSW |
15 |
73,691,199 (GRCm39) |
missense |
probably benign |
0.07 |
R0321:Mroh5
|
UTSW |
15 |
73,661,892 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Mroh5
|
UTSW |
15 |
73,662,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Mroh5
|
UTSW |
15 |
73,661,877 (GRCm39) |
missense |
probably benign |
0.01 |
R0707:Mroh5
|
UTSW |
15 |
73,662,588 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1666:Mroh5
|
UTSW |
15 |
73,659,754 (GRCm39) |
missense |
probably benign |
0.43 |
R1668:Mroh5
|
UTSW |
15 |
73,659,754 (GRCm39) |
missense |
probably benign |
0.43 |
R2139:Mroh5
|
UTSW |
15 |
73,661,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Mroh5
|
UTSW |
15 |
73,664,997 (GRCm39) |
missense |
probably benign |
0.02 |
R4078:Mroh5
|
UTSW |
15 |
73,657,889 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4420:Mroh5
|
UTSW |
15 |
73,654,923 (GRCm39) |
small deletion |
probably benign |
|
R4460:Mroh5
|
UTSW |
15 |
73,663,645 (GRCm39) |
missense |
probably damaging |
0.97 |
R4585:Mroh5
|
UTSW |
15 |
73,661,120 (GRCm39) |
missense |
probably benign |
0.38 |
R5285:Mroh5
|
UTSW |
15 |
73,654,923 (GRCm39) |
small deletion |
probably benign |
|
R5287:Mroh5
|
UTSW |
15 |
73,654,923 (GRCm39) |
small deletion |
probably benign |
|
R5437:Mroh5
|
UTSW |
15 |
73,659,818 (GRCm39) |
missense |
probably benign |
0.02 |
R5760:Mroh5
|
UTSW |
15 |
73,693,356 (GRCm39) |
missense |
probably damaging |
0.98 |
R5972:Mroh5
|
UTSW |
15 |
73,662,568 (GRCm39) |
critical splice donor site |
probably null |
|
R6192:Mroh5
|
UTSW |
15 |
73,662,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R6457:Mroh5
|
UTSW |
15 |
73,662,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R6477:Mroh5
|
UTSW |
15 |
73,662,604 (GRCm39) |
missense |
probably damaging |
1.00 |
R6776:Mroh5
|
UTSW |
15 |
73,661,817 (GRCm39) |
critical splice donor site |
probably null |
|
R7238:Mroh5
|
UTSW |
15 |
73,663,278 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7406:Mroh5
|
UTSW |
15 |
73,659,583 (GRCm39) |
missense |
probably benign |
0.38 |
R7853:Mroh5
|
UTSW |
15 |
73,663,189 (GRCm39) |
missense |
probably benign |
0.00 |
R7973:Mroh5
|
UTSW |
15 |
73,664,614 (GRCm39) |
nonsense |
probably null |
|
R8215:Mroh5
|
UTSW |
15 |
73,691,139 (GRCm39) |
missense |
probably damaging |
0.96 |
R8251:Mroh5
|
UTSW |
15 |
73,655,002 (GRCm39) |
missense |
probably benign |
0.01 |
R8771:Mroh5
|
UTSW |
15 |
73,693,203 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9032:Mroh5
|
UTSW |
15 |
73,655,302 (GRCm39) |
missense |
probably benign |
0.00 |
R9070:Mroh5
|
UTSW |
15 |
73,656,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R9238:Mroh5
|
UTSW |
15 |
73,663,586 (GRCm39) |
missense |
probably benign |
0.05 |
R9321:Mroh5
|
UTSW |
15 |
73,661,113 (GRCm39) |
missense |
probably benign |
0.00 |
X0024:Mroh5
|
UTSW |
15 |
73,659,570 (GRCm39) |
missense |
probably benign |
0.01 |
Z1088:Mroh5
|
UTSW |
15 |
73,659,880 (GRCm39) |
missense |
possibly damaging |
0.85 |
|