Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700008P02Rik |
A |
G |
3: 6,685,501 (GRCm39) |
|
probably benign |
Het |
Aadacl2 |
C |
T |
3: 59,917,997 (GRCm39) |
T82I |
probably benign |
Het |
Acadl |
T |
C |
1: 66,892,382 (GRCm39) |
N147S |
probably benign |
Het |
Actr3 |
A |
T |
1: 125,336,300 (GRCm39) |
M79K |
probably damaging |
Het |
Agbl3 |
A |
G |
6: 34,834,452 (GRCm39) |
S874G |
possibly damaging |
Het |
Aoah |
A |
T |
13: 21,187,118 (GRCm39) |
T472S |
probably damaging |
Het |
Asb16 |
A |
T |
11: 102,159,821 (GRCm39) |
D58V |
probably damaging |
Het |
B4galt1 |
T |
C |
4: 40,823,575 (GRCm39) |
D172G |
probably benign |
Het |
Bax |
T |
C |
7: 45,114,671 (GRCm39) |
N55S |
possibly damaging |
Het |
Bdkrb2 |
A |
G |
12: 105,558,118 (GRCm39) |
N120D |
possibly damaging |
Het |
Bicdl1 |
T |
C |
5: 115,789,325 (GRCm39) |
|
probably benign |
Het |
Cand1 |
A |
G |
10: 119,049,471 (GRCm39) |
L425P |
probably damaging |
Het |
Caskin1 |
G |
A |
17: 24,724,452 (GRCm39) |
|
probably null |
Het |
Cd248 |
C |
T |
19: 5,119,960 (GRCm39) |
P603S |
probably benign |
Het |
Cep95 |
G |
T |
11: 106,690,930 (GRCm39) |
R143L |
probably benign |
Het |
Clptm1l |
G |
T |
13: 73,762,792 (GRCm39) |
|
probably null |
Het |
Cntnap5a |
T |
C |
1: 115,987,930 (GRCm39) |
F154L |
possibly damaging |
Het |
Cyld |
A |
T |
8: 89,436,618 (GRCm39) |
I303F |
possibly damaging |
Het |
Dock2 |
A |
G |
11: 34,597,288 (GRCm39) |
S370P |
probably damaging |
Het |
Enah |
G |
T |
1: 181,749,858 (GRCm39) |
T327K |
probably damaging |
Het |
Farp2 |
A |
T |
1: 93,507,582 (GRCm39) |
S427C |
probably damaging |
Het |
Fbxw11 |
C |
T |
11: 32,683,612 (GRCm39) |
T301M |
probably damaging |
Het |
Foxc2 |
A |
T |
8: 121,843,915 (GRCm39) |
T188S |
probably benign |
Het |
Fzd2 |
A |
G |
11: 102,497,154 (GRCm39) |
T533A |
probably benign |
Het |
Glb1l2 |
G |
T |
9: 26,680,334 (GRCm39) |
S248* |
probably null |
Het |
Glul |
A |
T |
1: 153,781,284 (GRCm39) |
|
probably benign |
Het |
Gm28042 |
A |
G |
2: 119,871,887 (GRCm39) |
T946A |
probably benign |
Het |
Golga3 |
T |
A |
5: 110,329,649 (GRCm39) |
D2E |
probably damaging |
Het |
Grm1 |
A |
T |
10: 10,595,711 (GRCm39) |
F639Y |
probably benign |
Het |
Gzmn |
A |
G |
14: 56,403,368 (GRCm39) |
L247P |
probably benign |
Het |
Hgf |
T |
G |
5: 16,818,783 (GRCm39) |
I525R |
probably damaging |
Het |
Hnrnpul2 |
T |
A |
19: 8,808,696 (GRCm39) |
D719E |
probably benign |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Itga9 |
T |
C |
9: 118,436,185 (GRCm39) |
|
probably null |
Het |
Itgb1 |
T |
A |
8: 129,431,939 (GRCm39) |
C16S |
probably damaging |
Het |
Itgb1 |
G |
T |
8: 129,431,940 (GRCm39) |
C16F |
possibly damaging |
Het |
Kat14 |
A |
G |
2: 144,236,020 (GRCm39) |
I251V |
probably benign |
Het |
Kdsr |
A |
T |
1: 106,662,271 (GRCm39) |
|
probably null |
Het |
Kif12 |
T |
A |
4: 63,084,737 (GRCm39) |
E527V |
probably benign |
Het |
Larp1b |
T |
C |
3: 40,987,909 (GRCm39) |
S44P |
probably damaging |
Het |
Lonp2 |
T |
C |
8: 87,399,700 (GRCm39) |
|
probably benign |
Het |
Lrp1 |
C |
T |
10: 127,441,475 (GRCm39) |
S216N |
probably benign |
Het |
Lrrc19 |
T |
C |
4: 94,529,187 (GRCm39) |
S32G |
probably benign |
Het |
Mdm2 |
G |
A |
10: 117,526,434 (GRCm39) |
T335M |
probably benign |
Het |
Mettl25 |
A |
G |
10: 105,615,493 (GRCm39) |
Y504H |
probably damaging |
Het |
Mill1 |
T |
C |
7: 17,979,572 (GRCm39) |
I13T |
probably benign |
Het |
Mmachc |
T |
A |
4: 116,560,721 (GRCm39) |
Q258L |
probably benign |
Het |
Mpdz |
T |
A |
4: 81,339,413 (GRCm39) |
I5L |
probably benign |
Het |
Mrps2 |
C |
T |
2: 28,359,500 (GRCm39) |
A119V |
probably benign |
Het |
Mtcl2 |
A |
T |
2: 156,869,557 (GRCm39) |
M1026K |
probably benign |
Het |
Mtmr11 |
A |
G |
3: 96,075,429 (GRCm39) |
T370A |
probably benign |
Het |
Nmi |
T |
C |
2: 51,848,989 (GRCm39) |
I34V |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,926,901 (GRCm39) |
M5538K |
possibly damaging |
Het |
Ogdhl |
T |
C |
14: 32,047,822 (GRCm39) |
I24T |
probably benign |
Het |
Omp |
G |
T |
7: 97,794,566 (GRCm39) |
D20E |
probably benign |
Het |
Or2ag19 |
A |
G |
7: 106,444,403 (GRCm39) |
Y195C |
possibly damaging |
Het |
Or52e8b |
A |
G |
7: 104,673,767 (GRCm39) |
V140A |
probably benign |
Het |
Or5b120 |
C |
T |
19: 13,480,121 (GRCm39) |
T138M |
probably benign |
Het |
Or6c69 |
A |
G |
10: 129,747,550 (GRCm39) |
V199A |
probably benign |
Het |
Otog |
A |
G |
7: 45,933,332 (GRCm39) |
H1291R |
probably benign |
Het |
Pgbd1 |
A |
G |
13: 21,607,462 (GRCm39) |
L244P |
probably damaging |
Het |
Ranbp2 |
A |
G |
10: 58,299,808 (GRCm39) |
I481V |
probably benign |
Het |
Rbp3 |
A |
T |
14: 33,677,749 (GRCm39) |
I566F |
probably damaging |
Het |
Scn11a |
A |
G |
9: 119,598,873 (GRCm39) |
V1219A |
probably damaging |
Het |
Serpine3 |
G |
A |
14: 62,911,830 (GRCm39) |
G264D |
probably benign |
Het |
Slc4a10 |
T |
C |
2: 62,087,806 (GRCm39) |
F400L |
probably damaging |
Het |
Slco1a4 |
C |
T |
6: 141,791,173 (GRCm39) |
V8I |
probably benign |
Het |
Spen |
T |
C |
4: 141,215,335 (GRCm39) |
D499G |
unknown |
Het |
Stk32c |
A |
G |
7: 138,698,931 (GRCm39) |
|
probably null |
Het |
Tars1 |
A |
G |
15: 11,388,261 (GRCm39) |
V485A |
probably benign |
Het |
Tcerg1l |
A |
G |
7: 137,963,496 (GRCm39) |
L258P |
probably damaging |
Het |
Tmc2 |
A |
T |
2: 130,089,880 (GRCm39) |
I622F |
probably damaging |
Het |
Tmem183a |
A |
T |
1: 134,282,444 (GRCm39) |
N220K |
probably damaging |
Het |
Tnni3 |
T |
C |
7: 4,523,525 (GRCm39) |
D146G |
probably damaging |
Het |
Trappc11 |
G |
T |
8: 47,954,715 (GRCm39) |
D908E |
probably damaging |
Het |
Trappc8 |
A |
G |
18: 20,996,608 (GRCm39) |
Y436H |
probably damaging |
Het |
Ttc41 |
G |
A |
10: 86,612,254 (GRCm39) |
V1176I |
probably benign |
Het |
Ube2b |
A |
G |
11: 51,888,699 (GRCm39) |
V24A |
probably benign |
Het |
Usp30 |
T |
C |
5: 114,251,022 (GRCm39) |
C233R |
probably damaging |
Het |
Vmn1r87 |
T |
A |
7: 12,865,703 (GRCm39) |
T195S |
possibly damaging |
Het |
Vmn2r24 |
T |
C |
6: 123,783,479 (GRCm39) |
|
probably benign |
Het |
Vmn2r81 |
C |
A |
10: 79,128,858 (GRCm39) |
T583N |
probably damaging |
Het |
Vwa8 |
C |
T |
14: 79,145,670 (GRCm39) |
R116C |
probably damaging |
Het |
Wdr1 |
C |
A |
5: 38,687,315 (GRCm39) |
V239L |
probably benign |
Het |
Wdr17 |
C |
T |
8: 55,156,942 (GRCm39) |
|
probably benign |
Het |
Zfhx4 |
A |
C |
3: 5,306,789 (GRCm39) |
D5A |
probably damaging |
Het |
Zfyve27 |
T |
C |
19: 42,160,184 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Rsph4a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Rsph4a
|
APN |
10 |
33,790,339 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00536:Rsph4a
|
APN |
10 |
33,787,652 (GRCm39) |
splice site |
probably benign |
|
IGL00702:Rsph4a
|
APN |
10 |
33,789,068 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02313:Rsph4a
|
APN |
10 |
33,781,521 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL02556:Rsph4a
|
APN |
10 |
33,781,148 (GRCm39) |
utr 5 prime |
probably benign |
|
PIT4519001:Rsph4a
|
UTSW |
10 |
33,785,126 (GRCm39) |
missense |
probably benign |
0.09 |
R0006:Rsph4a
|
UTSW |
10 |
33,785,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R0006:Rsph4a
|
UTSW |
10 |
33,785,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R0088:Rsph4a
|
UTSW |
10 |
33,785,349 (GRCm39) |
missense |
probably benign |
0.15 |
R0513:Rsph4a
|
UTSW |
10 |
33,788,987 (GRCm39) |
nonsense |
probably null |
|
R1559:Rsph4a
|
UTSW |
10 |
33,785,727 (GRCm39) |
missense |
probably damaging |
0.99 |
R1783:Rsph4a
|
UTSW |
10 |
33,787,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R1914:Rsph4a
|
UTSW |
10 |
33,789,068 (GRCm39) |
missense |
probably damaging |
0.99 |
R2046:Rsph4a
|
UTSW |
10 |
33,790,539 (GRCm39) |
unclassified |
probably benign |
|
R2280:Rsph4a
|
UTSW |
10 |
33,787,595 (GRCm39) |
missense |
probably benign |
0.00 |
R2496:Rsph4a
|
UTSW |
10 |
33,784,094 (GRCm39) |
missense |
possibly damaging |
0.87 |
R3084:Rsph4a
|
UTSW |
10 |
33,785,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R3086:Rsph4a
|
UTSW |
10 |
33,785,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R4519:Rsph4a
|
UTSW |
10 |
33,787,623 (GRCm39) |
nonsense |
probably null |
|
R4965:Rsph4a
|
UTSW |
10 |
33,785,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5077:Rsph4a
|
UTSW |
10 |
33,784,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R5264:Rsph4a
|
UTSW |
10 |
33,785,379 (GRCm39) |
missense |
probably damaging |
1.00 |
R5359:Rsph4a
|
UTSW |
10 |
33,784,232 (GRCm39) |
missense |
probably benign |
0.08 |
R5464:Rsph4a
|
UTSW |
10 |
33,785,337 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5615:Rsph4a
|
UTSW |
10 |
33,785,324 (GRCm39) |
missense |
probably benign |
0.32 |
R5751:Rsph4a
|
UTSW |
10 |
33,781,789 (GRCm39) |
missense |
probably damaging |
0.99 |
R5763:Rsph4a
|
UTSW |
10 |
33,781,684 (GRCm39) |
missense |
probably damaging |
0.98 |
R5832:Rsph4a
|
UTSW |
10 |
33,785,498 (GRCm39) |
missense |
probably benign |
0.01 |
R6243:Rsph4a
|
UTSW |
10 |
33,785,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R6654:Rsph4a
|
UTSW |
10 |
33,788,988 (GRCm39) |
missense |
probably benign |
|
R6918:Rsph4a
|
UTSW |
10 |
33,781,272 (GRCm39) |
missense |
probably benign |
0.00 |
R7081:Rsph4a
|
UTSW |
10 |
33,785,189 (GRCm39) |
missense |
probably damaging |
0.97 |
R7453:Rsph4a
|
UTSW |
10 |
33,785,289 (GRCm39) |
missense |
probably benign |
0.00 |
R7611:Rsph4a
|
UTSW |
10 |
33,781,473 (GRCm39) |
missense |
probably benign |
0.15 |
R7670:Rsph4a
|
UTSW |
10 |
33,785,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R8017:Rsph4a
|
UTSW |
10 |
33,785,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R8495:Rsph4a
|
UTSW |
10 |
33,781,488 (GRCm39) |
missense |
probably benign |
0.00 |
R8806:Rsph4a
|
UTSW |
10 |
33,785,445 (GRCm39) |
missense |
probably damaging |
0.99 |
R8884:Rsph4a
|
UTSW |
10 |
33,781,840 (GRCm39) |
splice site |
probably benign |
|
R9171:Rsph4a
|
UTSW |
10 |
33,785,438 (GRCm39) |
nonsense |
probably null |
|
R9269:Rsph4a
|
UTSW |
10 |
33,785,394 (GRCm39) |
missense |
probably benign |
|
R9392:Rsph4a
|
UTSW |
10 |
33,781,236 (GRCm39) |
missense |
probably benign |
0.24 |
R9483:Rsph4a
|
UTSW |
10 |
33,790,418 (GRCm39) |
missense |
probably damaging |
1.00 |
X0057:Rsph4a
|
UTSW |
10 |
33,781,723 (GRCm39) |
missense |
possibly damaging |
0.58 |
X0066:Rsph4a
|
UTSW |
10 |
33,789,005 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Rsph4a
|
UTSW |
10 |
33,787,639 (GRCm39) |
missense |
probably damaging |
1.00 |
|