Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
C |
11: 109,827,590 (GRCm39) |
T1473A |
probably damaging |
Het |
Adam22 |
T |
C |
5: 8,217,393 (GRCm39) |
Y134C |
probably damaging |
Het |
Alg9 |
T |
A |
9: 50,699,524 (GRCm39) |
M183K |
probably damaging |
Het |
Ambra1 |
T |
C |
2: 91,602,655 (GRCm39) |
I213T |
possibly damaging |
Het |
Ankrd55 |
T |
A |
13: 112,504,466 (GRCm39) |
V376D |
probably benign |
Het |
Ano4 |
A |
C |
10: 88,948,807 (GRCm39) |
V166G |
probably benign |
Het |
Aox3 |
T |
A |
1: 58,202,583 (GRCm39) |
C730S |
probably benign |
Het |
Apc |
T |
A |
18: 34,446,016 (GRCm39) |
Y953N |
probably damaging |
Het |
Ass1 |
T |
C |
2: 31,391,544 (GRCm39) |
F273S |
possibly damaging |
Het |
Atg2b |
T |
C |
12: 105,610,135 (GRCm39) |
|
probably null |
Het |
B3gnt9 |
A |
G |
8: 105,981,122 (GRCm39) |
Y89H |
probably damaging |
Het |
Cd38 |
T |
G |
5: 44,063,506 (GRCm39) |
F200V |
probably damaging |
Het |
Cep170 |
G |
T |
1: 176,597,380 (GRCm39) |
R388S |
probably benign |
Het |
Col22a1 |
A |
T |
15: 71,816,271 (GRCm39) |
D614E |
probably damaging |
Het |
Crybg3 |
C |
A |
16: 59,378,463 (GRCm39) |
|
probably benign |
Het |
Ctdp1 |
A |
T |
18: 80,463,695 (GRCm39) |
S114T |
probably damaging |
Het |
Dctd |
C |
T |
8: 48,590,449 (GRCm39) |
|
probably benign |
Het |
Dmtf1 |
T |
C |
5: 9,172,439 (GRCm39) |
|
probably benign |
Het |
Dnhd1 |
G |
A |
7: 105,362,283 (GRCm39) |
V3715M |
probably damaging |
Het |
Dok1 |
A |
T |
6: 83,009,297 (GRCm39) |
L185H |
probably damaging |
Het |
Dpep1 |
T |
C |
8: 123,926,117 (GRCm39) |
V152A |
probably damaging |
Het |
Eif2ak1 |
G |
T |
5: 143,810,698 (GRCm39) |
R136L |
probably benign |
Het |
Eml5 |
A |
T |
12: 98,797,224 (GRCm39) |
S1063T |
probably damaging |
Het |
Fam171b |
T |
A |
2: 83,685,853 (GRCm39) |
L179* |
probably null |
Het |
Flot1 |
G |
T |
17: 36,135,267 (GRCm39) |
|
probably benign |
Het |
Fmn2 |
A |
T |
1: 174,571,866 (GRCm39) |
H1491L |
probably damaging |
Het |
Frem1 |
C |
T |
4: 82,859,049 (GRCm39) |
|
probably benign |
Het |
Gdf2 |
A |
G |
14: 33,666,863 (GRCm39) |
D195G |
probably benign |
Het |
Golga4 |
T |
G |
9: 118,387,368 (GRCm39) |
C1497G |
probably benign |
Het |
Gpaa1 |
T |
A |
15: 76,215,868 (GRCm39) |
C33* |
probably null |
Het |
Hectd1 |
A |
T |
12: 51,849,443 (GRCm39) |
C254S |
possibly damaging |
Het |
Hspa1b |
C |
T |
17: 35,177,086 (GRCm39) |
A300T |
probably benign |
Het |
Igf2bp2 |
A |
G |
16: 21,898,246 (GRCm39) |
I233T |
probably damaging |
Het |
Iqce |
C |
A |
5: 140,661,003 (GRCm39) |
A491S |
possibly damaging |
Het |
Irak3 |
A |
G |
10: 119,982,334 (GRCm39) |
|
probably null |
Het |
Kcnip1 |
T |
A |
11: 33,592,495 (GRCm39) |
H124L |
probably benign |
Het |
Klhdc10 |
G |
A |
6: 30,450,640 (GRCm39) |
R393Q |
probably benign |
Het |
Klhl28 |
C |
T |
12: 65,004,001 (GRCm39) |
E171K |
probably damaging |
Het |
Map2 |
T |
C |
1: 66,452,448 (GRCm39) |
V288A |
possibly damaging |
Het |
Mdp1 |
C |
T |
14: 55,896,683 (GRCm39) |
R126Q |
probably damaging |
Het |
Meltf |
A |
G |
16: 31,706,380 (GRCm39) |
D288G |
possibly damaging |
Het |
Mgat4e |
T |
A |
1: 134,468,890 (GRCm39) |
I385F |
probably benign |
Het |
Mical3 |
A |
C |
6: 121,015,030 (GRCm39) |
V211G |
probably damaging |
Het |
Mlh1 |
A |
G |
9: 111,100,478 (GRCm39) |
*39R |
probably null |
Het |
Mre11a |
A |
G |
9: 14,721,116 (GRCm39) |
D345G |
probably benign |
Het |
Mroh2a |
GCCC |
GC |
1: 88,159,979 (GRCm39) |
|
probably null |
Het |
Msh2 |
C |
A |
17: 88,030,841 (GRCm39) |
A906E |
probably benign |
Het |
Nat1 |
T |
G |
8: 67,944,077 (GRCm39) |
L154R |
probably benign |
Het |
Nlrp4a |
A |
G |
7: 26,161,905 (GRCm39) |
D851G |
probably damaging |
Het |
Npas4 |
A |
C |
19: 5,039,684 (GRCm39) |
V54G |
possibly damaging |
Het |
Or13n4 |
T |
C |
7: 106,423,364 (GRCm39) |
Y123C |
probably damaging |
Het |
Pcbp4 |
G |
A |
9: 106,339,292 (GRCm39) |
G100R |
probably damaging |
Het |
Pcdh17 |
A |
G |
14: 84,770,737 (GRCm39) |
T1072A |
probably benign |
Het |
Pcdh18 |
T |
C |
3: 49,708,906 (GRCm39) |
N803S |
probably benign |
Het |
Ppat |
C |
T |
5: 77,076,525 (GRCm39) |
|
probably benign |
Het |
Ppm1l |
T |
A |
3: 69,224,931 (GRCm39) |
L11Q |
probably damaging |
Het |
Pram1 |
T |
A |
17: 33,864,411 (GRCm39) |
V658E |
probably damaging |
Het |
Prr12 |
C |
T |
7: 44,699,225 (GRCm39) |
|
probably benign |
Het |
Prxl2b |
A |
G |
4: 154,981,531 (GRCm39) |
|
probably null |
Het |
Ptprq |
A |
G |
10: 107,444,137 (GRCm39) |
V1489A |
probably benign |
Het |
Ryr1 |
T |
A |
7: 28,768,540 (GRCm39) |
I2817F |
probably damaging |
Het |
Sall2 |
A |
G |
14: 52,551,950 (GRCm39) |
L413P |
probably damaging |
Het |
Slc7a9 |
T |
A |
7: 35,153,554 (GRCm39) |
M185K |
probably benign |
Het |
Stag2 |
C |
T |
X: 41,355,130 (GRCm39) |
H1149Y |
possibly damaging |
Het |
Timm10b |
T |
A |
7: 105,290,298 (GRCm39) |
Y64N |
probably damaging |
Het |
Tmem30c |
T |
C |
16: 57,086,868 (GRCm39) |
T312A |
probably benign |
Het |
Tmem9b |
G |
T |
7: 109,344,550 (GRCm39) |
C17* |
probably null |
Het |
Vmn2r68 |
C |
A |
7: 84,881,622 (GRCm39) |
R486L |
probably benign |
Het |
Xkr9 |
T |
A |
1: 13,771,387 (GRCm39) |
I301N |
probably damaging |
Het |
Xpo7 |
T |
C |
14: 70,925,704 (GRCm39) |
Q446R |
probably damaging |
Het |
Ythdf3 |
T |
C |
3: 16,259,362 (GRCm39) |
V503A |
possibly damaging |
Het |
Zfp280b |
T |
A |
10: 75,875,048 (GRCm39) |
V309D |
probably damaging |
Het |
Zfp53 |
T |
A |
17: 21,729,772 (GRCm39) |
C602S |
probably benign |
Het |
Zfp616 |
A |
T |
11: 73,974,643 (GRCm39) |
N395I |
possibly damaging |
Het |
Zfp644 |
T |
C |
5: 106,783,867 (GRCm39) |
I862M |
probably benign |
Het |
Zfp715 |
T |
C |
7: 42,949,019 (GRCm39) |
T314A |
possibly damaging |
Het |
|
Other mutations in 2310022A10Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02292:2310022A10Rik
|
APN |
7 |
27,263,982 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03261:2310022A10Rik
|
APN |
7 |
27,279,863 (GRCm39) |
nonsense |
probably null |
|
R0305:2310022A10Rik
|
UTSW |
7 |
27,274,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R1080:2310022A10Rik
|
UTSW |
7 |
27,265,109 (GRCm39) |
missense |
probably benign |
|
R1696:2310022A10Rik
|
UTSW |
7 |
27,260,022 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1773:2310022A10Rik
|
UTSW |
7 |
27,280,020 (GRCm39) |
missense |
probably damaging |
0.98 |
R4171:2310022A10Rik
|
UTSW |
7 |
27,265,109 (GRCm39) |
missense |
probably benign |
|
R4583:2310022A10Rik
|
UTSW |
7 |
27,274,017 (GRCm39) |
missense |
unknown |
|
R4781:2310022A10Rik
|
UTSW |
7 |
27,271,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R4806:2310022A10Rik
|
UTSW |
7 |
27,265,070 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4998:2310022A10Rik
|
UTSW |
7 |
27,271,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:2310022A10Rik
|
UTSW |
7 |
27,255,946 (GRCm39) |
missense |
probably benign |
0.04 |
R5008:2310022A10Rik
|
UTSW |
7 |
27,278,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R5364:2310022A10Rik
|
UTSW |
7 |
27,278,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R6119:2310022A10Rik
|
UTSW |
7 |
27,265,138 (GRCm39) |
nonsense |
probably null |
|
R6991:2310022A10Rik
|
UTSW |
7 |
27,279,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:2310022A10Rik
|
UTSW |
7 |
27,278,198 (GRCm39) |
nonsense |
probably null |
|
R7519:2310022A10Rik
|
UTSW |
7 |
27,274,155 (GRCm39) |
missense |
|
|
R7787:2310022A10Rik
|
UTSW |
7 |
27,263,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R8244:2310022A10Rik
|
UTSW |
7 |
27,271,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R8525:2310022A10Rik
|
UTSW |
7 |
27,255,936 (GRCm39) |
missense |
possibly damaging |
0.64 |
R9246:2310022A10Rik
|
UTSW |
7 |
27,279,961 (GRCm39) |
missense |
probably benign |
0.06 |
R9500:2310022A10Rik
|
UTSW |
7 |
27,265,091 (GRCm39) |
missense |
possibly damaging |
0.85 |
|