Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm2 |
G |
A |
3: 59,651,026 (GRCm39) |
M49I |
probably benign |
Het |
Acaca |
A |
G |
11: 84,105,084 (GRCm39) |
T147A |
possibly damaging |
Het |
Agbl3 |
A |
G |
6: 34,776,685 (GRCm39) |
D397G |
probably damaging |
Het |
Ank1 |
C |
T |
8: 23,625,654 (GRCm39) |
T1597M |
possibly damaging |
Het |
Arl4d |
A |
G |
11: 101,557,755 (GRCm39) |
T94A |
possibly damaging |
Het |
Cd22 |
A |
G |
7: 30,575,559 (GRCm39) |
I161T |
probably damaging |
Het |
Clcn7 |
C |
T |
17: 25,365,821 (GRCm39) |
L166F |
probably benign |
Het |
Cnbd1 |
G |
T |
4: 19,055,095 (GRCm39) |
N110K |
possibly damaging |
Het |
Col14a1 |
A |
T |
15: 55,327,165 (GRCm39) |
|
probably benign |
Het |
Col6a6 |
C |
T |
9: 105,661,300 (GRCm39) |
V270M |
probably damaging |
Het |
Cox8b |
C |
A |
7: 140,478,990 (GRCm39) |
G42W |
probably damaging |
Het |
Csn1s1 |
A |
T |
5: 87,828,704 (GRCm39) |
D275V |
probably benign |
Het |
Cubn |
T |
A |
2: 13,432,645 (GRCm39) |
|
probably null |
Het |
Dctn2 |
T |
C |
10: 127,111,690 (GRCm39) |
|
probably benign |
Het |
Dnm1l |
A |
G |
16: 16,160,604 (GRCm39) |
|
probably benign |
Het |
Dpp4 |
T |
C |
2: 62,164,988 (GRCm39) |
E687G |
probably benign |
Het |
Fbxw20 |
T |
C |
9: 109,052,377 (GRCm39) |
K249E |
possibly damaging |
Het |
Fhl2 |
C |
T |
1: 43,167,550 (GRCm39) |
W181* |
probably null |
Het |
G2e3 |
T |
A |
12: 51,415,941 (GRCm39) |
M559K |
probably benign |
Het |
Gdap1l1 |
A |
T |
2: 163,289,515 (GRCm39) |
Y160F |
possibly damaging |
Het |
Gm1110 |
T |
C |
9: 26,793,059 (GRCm39) |
I572M |
probably benign |
Het |
Gpatch2l |
T |
A |
12: 86,303,711 (GRCm39) |
|
probably benign |
Het |
Kcnq4 |
A |
G |
4: 120,573,051 (GRCm39) |
L250P |
probably damaging |
Het |
Lamc2 |
A |
T |
1: 153,041,962 (GRCm39) |
N57K |
probably benign |
Het |
Lingo1 |
A |
G |
9: 56,527,365 (GRCm39) |
L408P |
probably damaging |
Het |
Mmrn1 |
A |
T |
6: 60,954,131 (GRCm39) |
N804I |
possibly damaging |
Het |
Mroh7 |
A |
G |
4: 106,564,979 (GRCm39) |
L545S |
probably damaging |
Het |
Nup188 |
T |
A |
2: 30,213,648 (GRCm39) |
|
probably null |
Het |
Or10q1 |
A |
G |
19: 13,727,298 (GRCm39) |
D276G |
probably benign |
Het |
Or11a4 |
A |
G |
17: 37,536,217 (GRCm39) |
N67S |
probably damaging |
Het |
Or5b94 |
T |
C |
19: 12,651,602 (GRCm39) |
I11T |
probably damaging |
Het |
Pls1 |
A |
T |
9: 95,666,236 (GRCm39) |
N138K |
probably benign |
Het |
Prkch |
C |
A |
12: 73,749,286 (GRCm39) |
N345K |
probably benign |
Het |
Reps1 |
T |
C |
10: 17,931,865 (GRCm39) |
|
probably null |
Het |
Rrp7a |
T |
C |
15: 83,006,892 (GRCm39) |
E15G |
probably benign |
Het |
Scart2 |
A |
T |
7: 139,876,453 (GRCm39) |
N526Y |
probably damaging |
Het |
Scn1a |
T |
A |
2: 66,108,005 (GRCm39) |
T1557S |
possibly damaging |
Het |
Smtn |
T |
C |
11: 3,476,215 (GRCm39) |
E602G |
probably damaging |
Het |
Syvn1 |
T |
C |
19: 6,100,123 (GRCm39) |
|
probably null |
Het |
Tbxas1 |
A |
G |
6: 39,000,014 (GRCm39) |
D267G |
probably damaging |
Het |
Topbp1 |
A |
G |
9: 103,205,722 (GRCm39) |
N787D |
probably damaging |
Het |
Vmn2r22 |
T |
G |
6: 123,615,051 (GRCm39) |
S180R |
probably damaging |
Het |
Zfp345 |
T |
A |
2: 150,316,463 (GRCm39) |
E48D |
possibly damaging |
Het |
Zfp608 |
G |
A |
18: 55,030,509 (GRCm39) |
Q1144* |
probably null |
Het |
Zfp936 |
T |
A |
7: 42,836,691 (GRCm39) |
L34Q |
probably damaging |
Het |
|
Other mutations in A4gnt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00979:A4gnt
|
APN |
9 |
99,502,489 (GRCm39) |
nonsense |
probably null |
|
IGL01509:A4gnt
|
APN |
9 |
99,495,819 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03339:A4gnt
|
APN |
9 |
99,502,601 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4466001:A4gnt
|
UTSW |
9 |
99,502,613 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4472001:A4gnt
|
UTSW |
9 |
99,502,613 (GRCm39) |
missense |
probably damaging |
0.99 |
R2027:A4gnt
|
UTSW |
9 |
99,502,254 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2061:A4gnt
|
UTSW |
9 |
99,502,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R4130:A4gnt
|
UTSW |
9 |
99,502,671 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4131:A4gnt
|
UTSW |
9 |
99,502,671 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5249:A4gnt
|
UTSW |
9 |
99,502,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R5338:A4gnt
|
UTSW |
9 |
99,502,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R5672:A4gnt
|
UTSW |
9 |
99,502,383 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5785:A4gnt
|
UTSW |
9 |
99,502,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R6519:A4gnt
|
UTSW |
9 |
99,495,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R6630:A4gnt
|
UTSW |
9 |
99,495,971 (GRCm39) |
missense |
probably benign |
0.00 |
R7296:A4gnt
|
UTSW |
9 |
99,502,335 (GRCm39) |
missense |
probably damaging |
0.97 |
R7514:A4gnt
|
UTSW |
9 |
99,502,598 (GRCm39) |
missense |
probably benign |
0.05 |
R7731:A4gnt
|
UTSW |
9 |
99,502,470 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9311:A4gnt
|
UTSW |
9 |
99,495,816 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9786:A4gnt
|
UTSW |
9 |
99,502,536 (GRCm39) |
missense |
possibly damaging |
0.65 |
Z1088:A4gnt
|
UTSW |
9 |
99,495,894 (GRCm39) |
missense |
probably damaging |
0.97 |
|