Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
T |
C |
7: 130,959,242 (GRCm39) |
R153G |
probably benign |
Het |
5730596B20Rik |
C |
A |
6: 52,155,962 (GRCm39) |
Y9* |
probably null |
Het |
Aco1 |
G |
A |
4: 40,183,605 (GRCm39) |
G508S |
probably damaging |
Het |
Acot3 |
A |
G |
12: 84,100,230 (GRCm39) |
H2R |
possibly damaging |
Het |
Adamts13 |
T |
A |
2: 26,896,326 (GRCm39) |
C1240S |
probably damaging |
Het |
Adra1b |
T |
C |
11: 43,726,698 (GRCm39) |
N73S |
probably damaging |
Het |
Aebp2 |
G |
A |
6: 140,579,420 (GRCm39) |
S219N |
probably benign |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Ank |
T |
C |
15: 27,565,108 (GRCm39) |
S270P |
probably benign |
Het |
Ankle1 |
G |
A |
8: 71,861,973 (GRCm39) |
R492H |
possibly damaging |
Het |
Ankub1 |
G |
A |
3: 57,599,713 (GRCm39) |
H19Y |
possibly damaging |
Het |
Anln |
C |
A |
9: 22,244,464 (GRCm39) |
W1083L |
probably benign |
Het |
Apaf1 |
G |
T |
10: 90,867,556 (GRCm39) |
S763* |
probably null |
Het |
Apba3 |
A |
G |
10: 81,105,128 (GRCm39) |
T134A |
probably benign |
Het |
Bod1l |
C |
T |
5: 41,976,532 (GRCm39) |
S1594N |
probably benign |
Het |
C7 |
T |
C |
15: 5,019,910 (GRCm39) |
M746V |
probably benign |
Het |
Cdkn2a |
T |
A |
4: 89,212,730 (GRCm39) |
I11F |
possibly damaging |
Het |
Cideb |
T |
C |
14: 55,992,617 (GRCm39) |
M100V |
possibly damaging |
Het |
Cntnap5c |
T |
C |
17: 58,612,547 (GRCm39) |
L862P |
possibly damaging |
Het |
Coch |
A |
T |
12: 51,649,472 (GRCm39) |
D261V |
probably benign |
Het |
Cyp2ab1 |
A |
G |
16: 20,132,639 (GRCm39) |
F220L |
possibly damaging |
Het |
Ddx10 |
A |
T |
9: 53,151,805 (GRCm39) |
D73E |
probably benign |
Het |
Dgkg |
A |
G |
16: 22,384,067 (GRCm39) |
F462S |
probably damaging |
Het |
Dlgap3 |
C |
T |
4: 127,089,159 (GRCm39) |
H252Y |
probably damaging |
Het |
Dmd |
G |
C |
X: 83,356,089 (GRCm39) |
A2257P |
probably benign |
Het |
Dnaaf6rt |
A |
G |
1: 31,262,077 (GRCm39) |
S20G |
probably benign |
Het |
Dnai4 |
G |
A |
4: 102,907,390 (GRCm39) |
T632M |
probably damaging |
Het |
Dtnb |
A |
G |
12: 3,831,273 (GRCm39) |
T658A |
probably benign |
Het |
Duox2 |
T |
A |
2: 122,125,639 (GRCm39) |
S323C |
probably damaging |
Het |
Dync1h1 |
T |
A |
12: 110,581,026 (GRCm39) |
I251N |
probably damaging |
Het |
Eml5 |
A |
G |
12: 98,768,705 (GRCm39) |
S1457P |
probably damaging |
Het |
Fam114a1 |
T |
A |
5: 65,153,247 (GRCm39) |
|
probably null |
Het |
Fcho1 |
A |
T |
8: 72,163,133 (GRCm39) |
L632Q |
probably damaging |
Het |
Gm12695 |
T |
C |
4: 96,612,182 (GRCm39) |
Y527C |
possibly damaging |
Het |
Gm16223 |
T |
C |
5: 42,371,942 (GRCm39) |
C111R |
unknown |
Het |
H2-Q4 |
T |
A |
17: 35,599,378 (GRCm39) |
S154T |
possibly damaging |
Het |
Hhat |
A |
G |
1: 192,409,687 (GRCm39) |
F125L |
possibly damaging |
Het |
Ier5l |
T |
A |
2: 30,363,068 (GRCm39) |
D319V |
probably damaging |
Het |
Kif5a |
T |
C |
10: 127,081,238 (GRCm39) |
D232G |
probably damaging |
Het |
M1ap |
A |
G |
6: 82,958,863 (GRCm39) |
I165V |
probably benign |
Het |
Map2k4 |
A |
C |
11: 65,584,282 (GRCm39) |
F334V |
probably damaging |
Het |
Mmp19 |
G |
A |
10: 128,630,848 (GRCm39) |
R156H |
probably damaging |
Het |
Mpped2 |
T |
A |
2: 106,575,147 (GRCm39) |
Y77* |
probably null |
Het |
Nhs |
T |
A |
X: 160,625,717 (GRCm39) |
H544L |
probably damaging |
Het |
Nr4a1 |
C |
A |
15: 101,171,948 (GRCm39) |
H541N |
probably damaging |
Het |
Or4a74 |
A |
G |
2: 89,439,822 (GRCm39) |
V208A |
probably benign |
Het |
Or5b122 |
A |
T |
19: 13,562,965 (GRCm39) |
Q99L |
probably damaging |
Het |
Pak6 |
A |
C |
2: 118,519,332 (GRCm39) |
N17T |
probably damaging |
Het |
Pcnt |
T |
A |
10: 76,216,214 (GRCm39) |
T2225S |
possibly damaging |
Het |
Pdzd2 |
A |
G |
15: 12,385,905 (GRCm39) |
L955P |
probably damaging |
Het |
Phf21a |
A |
G |
2: 92,178,381 (GRCm39) |
D357G |
probably damaging |
Het |
Pkhd1l1 |
G |
T |
15: 44,422,035 (GRCm39) |
A3102S |
probably damaging |
Het |
Plch2 |
A |
T |
4: 155,074,366 (GRCm39) |
L754Q |
probably damaging |
Het |
Plekhd1 |
A |
G |
12: 80,768,066 (GRCm39) |
N335D |
probably benign |
Het |
Pole |
C |
A |
5: 110,473,417 (GRCm39) |
T1737N |
probably damaging |
Het |
Potefam1 |
T |
C |
2: 111,030,763 (GRCm39) |
E382G |
probably damaging |
Het |
Pramel6 |
G |
A |
2: 87,339,088 (GRCm39) |
S96N |
probably damaging |
Het |
Prdm14 |
A |
C |
1: 13,195,954 (GRCm39) |
Y36D |
possibly damaging |
Het |
Psg27 |
T |
C |
7: 18,294,342 (GRCm39) |
D355G |
probably damaging |
Het |
Rfc1 |
A |
T |
5: 65,459,282 (GRCm39) |
D225E |
probably damaging |
Het |
Sec16a |
A |
G |
2: 26,330,251 (GRCm39) |
I588T |
probably damaging |
Het |
Setd6 |
G |
A |
8: 96,443,416 (GRCm39) |
V60M |
probably damaging |
Het |
Sgk3 |
A |
G |
1: 9,961,649 (GRCm39) |
I432V |
probably benign |
Het |
Six2 |
A |
G |
17: 85,994,933 (GRCm39) |
S150P |
probably damaging |
Het |
Slc1a6 |
T |
C |
10: 78,635,964 (GRCm39) |
V343A |
possibly damaging |
Het |
Slc43a3 |
T |
C |
2: 84,774,956 (GRCm39) |
|
probably null |
Het |
Smc3 |
A |
G |
19: 53,619,964 (GRCm39) |
D620G |
probably benign |
Het |
Smg6 |
C |
G |
11: 74,821,120 (GRCm39) |
P464A |
probably damaging |
Het |
Sox11 |
T |
C |
12: 27,392,278 (GRCm39) |
T44A |
possibly damaging |
Het |
Spata22 |
A |
G |
11: 73,227,052 (GRCm39) |
R89G |
possibly damaging |
Het |
Spmip6 |
A |
G |
4: 41,507,519 (GRCm39) |
|
probably null |
Het |
Stk3 |
T |
C |
15: 34,959,195 (GRCm39) |
M256V |
possibly damaging |
Het |
Syne2 |
A |
G |
12: 76,062,353 (GRCm39) |
D4226G |
possibly damaging |
Het |
Tecpr2 |
T |
C |
12: 110,934,863 (GRCm39) |
S1370P |
possibly damaging |
Het |
Tek |
A |
G |
4: 94,715,966 (GRCm39) |
I463V |
probably benign |
Het |
Trib1 |
T |
A |
15: 59,526,189 (GRCm39) |
I253N |
probably damaging |
Het |
Triobp |
G |
T |
15: 78,858,095 (GRCm39) |
G1232V |
probably damaging |
Het |
Trpm6 |
G |
A |
19: 18,853,406 (GRCm39) |
V1809M |
probably damaging |
Het |
Tsc22d4 |
A |
G |
5: 137,760,749 (GRCm39) |
K57E |
possibly damaging |
Het |
Vmn2r109 |
T |
A |
17: 20,784,974 (GRCm39) |
K15N |
probably benign |
Het |
Wnt9a |
A |
G |
11: 59,222,055 (GRCm39) |
N318D |
probably damaging |
Het |
Wwp1 |
A |
G |
4: 19,662,181 (GRCm39) |
V138A |
possibly damaging |
Het |
Zfp37 |
A |
T |
4: 62,109,945 (GRCm39) |
M411K |
probably damaging |
Het |
Zfp715 |
T |
A |
7: 42,960,544 (GRCm39) |
T16S |
probably benign |
Het |
Zfp932 |
A |
G |
5: 110,157,684 (GRCm39) |
T461A |
possibly damaging |
Het |
Zscan29 |
A |
T |
2: 120,991,336 (GRCm39) |
C817* |
probably null |
Het |
|
Other mutations in Armh3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Armh3
|
APN |
19 |
45,928,927 (GRCm39) |
missense |
probably benign |
0.19 |
IGL00788:Armh3
|
APN |
19 |
45,920,789 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01356:Armh3
|
APN |
19 |
45,954,742 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01477:Armh3
|
APN |
19 |
45,967,043 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01660:Armh3
|
APN |
19 |
45,928,915 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02193:Armh3
|
APN |
19 |
45,961,323 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02863:Armh3
|
APN |
19 |
45,946,850 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03108:Armh3
|
APN |
19 |
45,808,792 (GRCm39) |
missense |
probably damaging |
0.99 |
R0035:Armh3
|
UTSW |
19 |
45,879,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R0791:Armh3
|
UTSW |
19 |
45,922,307 (GRCm39) |
splice site |
probably null |
|
R0792:Armh3
|
UTSW |
19 |
45,922,307 (GRCm39) |
splice site |
probably null |
|
R1487:Armh3
|
UTSW |
19 |
45,928,882 (GRCm39) |
critical splice donor site |
probably null |
|
R1843:Armh3
|
UTSW |
19 |
45,963,691 (GRCm39) |
missense |
probably benign |
0.17 |
R2061:Armh3
|
UTSW |
19 |
45,967,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R2070:Armh3
|
UTSW |
19 |
45,879,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R2072:Armh3
|
UTSW |
19 |
45,953,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2074:Armh3
|
UTSW |
19 |
45,953,820 (GRCm39) |
missense |
probably damaging |
0.99 |
R2091:Armh3
|
UTSW |
19 |
45,941,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R2263:Armh3
|
UTSW |
19 |
45,920,788 (GRCm39) |
critical splice donor site |
probably null |
|
R2863:Armh3
|
UTSW |
19 |
45,874,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:Armh3
|
UTSW |
19 |
45,963,722 (GRCm39) |
splice site |
probably benign |
|
R3796:Armh3
|
UTSW |
19 |
45,910,049 (GRCm39) |
splice site |
probably benign |
|
R4044:Armh3
|
UTSW |
19 |
45,808,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Armh3
|
UTSW |
19 |
45,948,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Armh3
|
UTSW |
19 |
45,808,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R4983:Armh3
|
UTSW |
19 |
45,939,146 (GRCm39) |
missense |
probably benign |
|
R5063:Armh3
|
UTSW |
19 |
45,874,394 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5313:Armh3
|
UTSW |
19 |
45,807,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R5782:Armh3
|
UTSW |
19 |
45,874,466 (GRCm39) |
missense |
probably benign |
0.08 |
R5985:Armh3
|
UTSW |
19 |
45,808,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R6220:Armh3
|
UTSW |
19 |
45,834,554 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6379:Armh3
|
UTSW |
19 |
45,910,136 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6674:Armh3
|
UTSW |
19 |
45,963,437 (GRCm39) |
missense |
probably benign |
0.06 |
R6842:Armh3
|
UTSW |
19 |
45,807,416 (GRCm39) |
missense |
probably benign |
0.05 |
R6890:Armh3
|
UTSW |
19 |
45,948,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R7034:Armh3
|
UTSW |
19 |
45,953,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R7036:Armh3
|
UTSW |
19 |
45,953,688 (GRCm39) |
missense |
probably damaging |
0.98 |
R7305:Armh3
|
UTSW |
19 |
45,880,560 (GRCm39) |
missense |
probably benign |
0.35 |
R7411:Armh3
|
UTSW |
19 |
45,953,874 (GRCm39) |
missense |
probably benign |
0.00 |
R7762:Armh3
|
UTSW |
19 |
45,928,882 (GRCm39) |
critical splice donor site |
probably null |
|
R8021:Armh3
|
UTSW |
19 |
45,945,180 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8366:Armh3
|
UTSW |
19 |
45,920,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R9336:Armh3
|
UTSW |
19 |
45,945,120 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Armh3
|
UTSW |
19 |
45,920,832 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1088:Armh3
|
UTSW |
19 |
45,807,344 (GRCm39) |
missense |
probably damaging |
1.00 |
|