Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam15 |
A |
G |
3: 89,252,663 (GRCm39) |
S309P |
probably damaging |
Het |
Agtpbp1 |
A |
T |
13: 59,630,415 (GRCm39) |
M772K |
possibly damaging |
Het |
Ankfn1 |
T |
C |
11: 89,282,442 (GRCm39) |
M402V |
probably benign |
Het |
Anln |
G |
A |
9: 22,269,418 (GRCm39) |
T822I |
possibly damaging |
Het |
Atp13a4 |
A |
G |
16: 29,260,125 (GRCm39) |
V589A |
probably benign |
Het |
Ccm2l |
C |
T |
2: 152,909,779 (GRCm39) |
L44F |
probably damaging |
Het |
Cd177 |
A |
T |
7: 24,443,818 (GRCm39) |
L760Q |
probably damaging |
Het |
Cd177 |
G |
T |
7: 24,443,819 (GRCm39) |
L760M |
probably damaging |
Het |
Cfap69 |
T |
C |
5: 5,714,017 (GRCm39) |
E5G |
probably benign |
Het |
Col4a1 |
G |
A |
8: 11,271,375 (GRCm39) |
T753I |
probably benign |
Het |
Col6a3 |
T |
A |
1: 90,731,600 (GRCm39) |
D1551V |
probably damaging |
Het |
Ddx20 |
A |
G |
3: 105,586,593 (GRCm39) |
V584A |
probably benign |
Het |
Dop1a |
C |
A |
9: 86,402,209 (GRCm39) |
H1136Q |
probably benign |
Het |
Egf |
T |
C |
3: 129,496,128 (GRCm39) |
E329G |
probably damaging |
Het |
Eif3c |
A |
G |
7: 126,157,831 (GRCm39) |
V337A |
probably benign |
Het |
Eif3f |
G |
T |
7: 108,533,881 (GRCm39) |
|
probably benign |
Het |
Eif3f |
C |
T |
7: 108,533,882 (GRCm39) |
|
probably benign |
Het |
Evc |
T |
A |
5: 37,483,740 (GRCm39) |
I187F |
probably benign |
Het |
Fam117a |
T |
G |
11: 95,254,815 (GRCm39) |
|
probably benign |
Het |
H2-M10.4 |
A |
T |
17: 36,771,323 (GRCm39) |
V285E |
probably damaging |
Het |
Hps4 |
G |
T |
5: 112,523,307 (GRCm39) |
M608I |
probably benign |
Het |
Idh3b |
T |
A |
2: 130,126,321 (GRCm39) |
N6I |
probably benign |
Het |
Itgam |
A |
T |
7: 127,675,281 (GRCm39) |
M169L |
probably damaging |
Het |
Kcnn3 |
G |
A |
3: 89,570,029 (GRCm39) |
G614D |
possibly damaging |
Het |
Kcnn3 |
A |
G |
3: 89,428,281 (GRCm39) |
N169S |
possibly damaging |
Het |
Mn1 |
A |
T |
5: 111,569,717 (GRCm39) |
K1229M |
probably damaging |
Het |
Ms4a19 |
A |
G |
19: 11,118,897 (GRCm39) |
*71Q |
probably null |
Het |
Nckap5 |
A |
G |
1: 125,955,553 (GRCm39) |
M401T |
probably damaging |
Het |
Or1af1 |
T |
C |
2: 37,110,112 (GRCm39) |
S204P |
probably damaging |
Het |
Or8c13 |
T |
C |
9: 38,091,964 (GRCm39) |
N52D |
possibly damaging |
Het |
Or8d4 |
T |
G |
9: 40,038,561 (GRCm39) |
E232A |
probably benign |
Het |
Pttg1ip2 |
G |
A |
5: 5,502,039 (GRCm39) |
Q138* |
probably null |
Het |
Sim2 |
G |
A |
16: 93,898,047 (GRCm39) |
V94M |
probably damaging |
Het |
Slc46a3 |
G |
A |
5: 147,822,822 (GRCm39) |
T340M |
probably benign |
Het |
Ssc4d |
A |
G |
5: 135,994,923 (GRCm39) |
|
probably benign |
Het |
Trav12-1 |
A |
G |
14: 53,775,916 (GRCm39) |
D22G |
probably damaging |
Het |
Trgv4 |
T |
A |
13: 19,369,422 (GRCm39) |
D55E |
possibly damaging |
Het |
Trps1 |
G |
A |
15: 50,524,273 (GRCm39) |
T969M |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,719,894 (GRCm39) |
|
probably benign |
Het |
Ubqln4 |
A |
G |
3: 88,470,458 (GRCm39) |
N310S |
probably benign |
Het |
Vapa |
T |
C |
17: 65,889,756 (GRCm39) |
|
probably benign |
Het |
Vmn1r65 |
T |
C |
7: 6,011,893 (GRCm39) |
T114A |
possibly damaging |
Het |
Vps13d |
T |
C |
4: 144,875,332 (GRCm39) |
E1725G |
probably damaging |
Het |
Vps53 |
A |
G |
11: 76,027,143 (GRCm39) |
|
probably benign |
Het |
Xkr9 |
T |
C |
1: 13,742,799 (GRCm39) |
L28P |
probably damaging |
Het |
|
Other mutations in 4930474N05Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01393:4930474N05Rik
|
APN |
14 |
35,818,379 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01694:4930474N05Rik
|
APN |
14 |
35,818,659 (GRCm39) |
makesense |
probably null |
|
R0071:4930474N05Rik
|
UTSW |
14 |
35,812,746 (GRCm39) |
unclassified |
probably benign |
|
R0537:4930474N05Rik
|
UTSW |
14 |
35,818,657 (GRCm39) |
missense |
probably benign |
0.07 |
R0960:4930474N05Rik
|
UTSW |
14 |
35,818,367 (GRCm39) |
missense |
probably benign |
0.01 |
R1919:4930474N05Rik
|
UTSW |
14 |
35,817,414 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2338:4930474N05Rik
|
UTSW |
14 |
35,817,109 (GRCm39) |
missense |
probably benign |
|
R3837:4930474N05Rik
|
UTSW |
14 |
35,817,435 (GRCm39) |
missense |
probably benign |
0.03 |
R4192:4930474N05Rik
|
UTSW |
14 |
35,818,536 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4193:4930474N05Rik
|
UTSW |
14 |
35,818,536 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4526:4930474N05Rik
|
UTSW |
14 |
35,818,535 (GRCm39) |
missense |
probably damaging |
1.00 |
R7007:4930474N05Rik
|
UTSW |
14 |
35,817,121 (GRCm39) |
missense |
probably benign |
0.18 |
R7302:4930474N05Rik
|
UTSW |
14 |
35,817,306 (GRCm39) |
missense |
probably benign |
0.00 |
R7998:4930474N05Rik
|
UTSW |
14 |
35,818,649 (GRCm39) |
missense |
probably benign |
0.22 |
R8202:4930474N05Rik
|
UTSW |
14 |
35,817,057 (GRCm39) |
missense |
probably benign |
0.01 |
R8714:4930474N05Rik
|
UTSW |
14 |
35,818,456 (GRCm39) |
nonsense |
probably null |
|
|