Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
T |
C |
16: 90,852,551 (GRCm39) |
Y195C |
probably damaging |
Het |
Abcb1a |
T |
A |
5: 8,735,371 (GRCm39) |
F159L |
probably damaging |
Het |
Adam6b |
A |
G |
12: 113,454,371 (GRCm39) |
N396S |
probably benign |
Het |
Adamts15 |
T |
C |
9: 30,823,055 (GRCm39) |
M338V |
possibly damaging |
Het |
Adamts7 |
T |
A |
9: 90,077,321 (GRCm39) |
H1329Q |
probably damaging |
Het |
Aim2 |
C |
T |
1: 173,289,786 (GRCm39) |
P243L |
probably damaging |
Het |
Ankdd1a |
T |
C |
9: 65,412,418 (GRCm39) |
D311G |
probably damaging |
Het |
Apon |
A |
T |
10: 128,090,428 (GRCm39) |
E35D |
probably benign |
Het |
Atp1a4 |
T |
C |
1: 172,078,566 (GRCm39) |
D224G |
probably damaging |
Het |
Atp6v0a1 |
T |
A |
11: 100,953,229 (GRCm39) |
*839R |
probably null |
Het |
Bco2 |
A |
G |
9: 50,461,878 (GRCm39) |
L42P |
probably damaging |
Het |
Bicral |
T |
A |
17: 47,141,873 (GRCm39) |
|
probably benign |
Het |
Ccna1 |
T |
C |
3: 54,955,878 (GRCm39) |
Q306R |
probably benign |
Het |
Cep152 |
G |
T |
2: 125,406,131 (GRCm39) |
S1467* |
probably null |
Het |
Cfap44 |
T |
A |
16: 44,225,085 (GRCm39) |
V110E |
probably damaging |
Het |
Clip2 |
G |
A |
5: 134,531,462 (GRCm39) |
A781V |
probably benign |
Het |
Cps1 |
A |
T |
1: 67,243,772 (GRCm39) |
I1083F |
probably damaging |
Het |
Cux1 |
A |
G |
5: 136,336,710 (GRCm39) |
V934A |
possibly damaging |
Het |
Depdc5 |
T |
C |
5: 33,101,382 (GRCm39) |
F891L |
possibly damaging |
Het |
Dnai7 |
T |
A |
6: 145,127,542 (GRCm39) |
I456F |
probably benign |
Het |
Dnajc13 |
A |
G |
9: 104,057,338 (GRCm39) |
V1554A |
probably benign |
Het |
Echs1 |
A |
T |
7: 139,690,499 (GRCm39) |
M191K |
probably damaging |
Het |
Eif6 |
T |
A |
2: 155,664,772 (GRCm39) |
D238V |
probably benign |
Het |
Fat2 |
G |
A |
11: 55,144,692 (GRCm39) |
L4061F |
probably benign |
Het |
Fat3 |
T |
C |
9: 15,908,703 (GRCm39) |
D2433G |
probably damaging |
Het |
Flt3 |
A |
G |
5: 147,320,265 (GRCm39) |
V33A |
probably benign |
Het |
Garin2 |
TGATGTCACAGATGTCAC |
TGATGTCAC |
12: 78,762,057 (GRCm39) |
|
probably benign |
Het |
Gpr155 |
T |
C |
2: 73,174,039 (GRCm39) |
E790G |
probably damaging |
Het |
Ighv1-67 |
A |
T |
12: 115,567,861 (GRCm39) |
V17E |
probably damaging |
Het |
Klra9 |
T |
A |
6: 130,165,639 (GRCm39) |
R125S |
probably damaging |
Het |
Leo1 |
T |
C |
9: 75,353,277 (GRCm39) |
|
probably null |
Het |
Map2 |
G |
T |
1: 66,460,872 (GRCm39) |
R1556L |
probably damaging |
Het |
Megf8 |
A |
G |
7: 25,059,166 (GRCm39) |
|
probably null |
Het |
Meikin |
T |
C |
11: 54,317,477 (GRCm39) |
I426T |
possibly damaging |
Het |
Muc16 |
A |
T |
9: 18,556,015 (GRCm39) |
V3426E |
unknown |
Het |
Or51af1 |
G |
A |
7: 103,142,029 (GRCm39) |
L19F |
probably damaging |
Het |
Or52n2c |
A |
G |
7: 104,574,620 (GRCm39) |
L117P |
probably damaging |
Het |
Or7e168 |
T |
G |
9: 19,720,105 (GRCm39) |
S164A |
possibly damaging |
Het |
Or8k25 |
T |
C |
2: 86,243,935 (GRCm39) |
I154V |
probably benign |
Het |
Or9s13 |
T |
C |
1: 92,547,643 (GRCm39) |
V5A |
probably benign |
Het |
Otogl |
A |
G |
10: 107,747,936 (GRCm39) |
|
probably null |
Het |
Palm3 |
T |
C |
8: 84,756,504 (GRCm39) |
L672P |
probably damaging |
Het |
Perm1 |
A |
G |
4: 156,302,091 (GRCm39) |
T212A |
probably benign |
Het |
Poc1a |
T |
C |
9: 106,226,960 (GRCm39) |
M400T |
probably benign |
Het |
Pou6f2 |
T |
A |
13: 18,414,196 (GRCm39) |
Q193L |
unknown |
Het |
Ppl |
C |
T |
16: 4,905,300 (GRCm39) |
R1665H |
probably benign |
Het |
Ppp4r3b |
T |
C |
11: 29,123,449 (GRCm39) |
|
probably null |
Het |
Ptger1 |
T |
C |
8: 84,394,654 (GRCm39) |
S44P |
probably damaging |
Het |
Pzp |
T |
C |
6: 128,473,009 (GRCm39) |
T787A |
probably benign |
Het |
Rab44 |
A |
T |
17: 29,358,642 (GRCm39) |
R277* |
probably null |
Het |
Rasgef1a |
T |
A |
6: 118,064,088 (GRCm39) |
I334K |
probably damaging |
Het |
Rfx1 |
T |
C |
8: 84,818,084 (GRCm39) |
V554A |
possibly damaging |
Het |
Ripk1 |
T |
A |
13: 34,214,032 (GRCm39) |
I518K |
possibly damaging |
Het |
Rpl22 |
A |
G |
4: 152,416,763 (GRCm39) |
Y90C |
probably damaging |
Het |
Rps27a |
C |
A |
11: 29,495,998 (GRCm39) |
R118L |
probably benign |
Het |
Scmh1 |
T |
A |
4: 120,319,331 (GRCm39) |
S19T |
probably benign |
Het |
Scn10a |
C |
T |
9: 119,520,509 (GRCm39) |
|
probably null |
Het |
Sema4c |
A |
T |
1: 36,589,867 (GRCm39) |
S496T |
probably benign |
Het |
Serpina3i |
T |
C |
12: 104,231,387 (GRCm39) |
V8A |
possibly damaging |
Het |
Sis |
G |
A |
3: 72,867,628 (GRCm39) |
T139M |
probably damaging |
Het |
Skic3 |
A |
T |
13: 76,303,587 (GRCm39) |
H1227L |
probably benign |
Het |
Slc45a2 |
T |
A |
15: 11,000,972 (GRCm39) |
S24T |
probably benign |
Het |
Slc5a11 |
A |
G |
7: 122,866,975 (GRCm39) |
I423M |
probably benign |
Het |
Slc7a10 |
G |
A |
7: 34,885,997 (GRCm39) |
G31S |
probably benign |
Het |
Sowahc |
A |
G |
10: 59,059,001 (GRCm39) |
N379S |
probably benign |
Het |
Stat5a |
T |
C |
11: 100,774,714 (GRCm39) |
M741T |
unknown |
Het |
Tcf15 |
T |
C |
2: 151,986,020 (GRCm39) |
S159P |
probably benign |
Het |
Tdrd5 |
C |
A |
1: 156,098,788 (GRCm39) |
R669L |
possibly damaging |
Het |
Tln1 |
T |
C |
4: 43,553,041 (GRCm39) |
E350G |
possibly damaging |
Het |
Trim12c |
T |
G |
7: 103,997,271 (GRCm39) |
N95T |
|
Het |
Urb1 |
T |
C |
16: 90,571,513 (GRCm39) |
T1099A |
probably benign |
Het |
Vmn1r44 |
T |
A |
6: 89,870,578 (GRCm39) |
V108D |
probably damaging |
Het |
Vmn2r65 |
A |
G |
7: 84,589,388 (GRCm39) |
Y843H |
probably benign |
Het |
Vmn2r68 |
A |
G |
7: 84,871,321 (GRCm39) |
I654T |
possibly damaging |
Het |
Vps13a |
T |
C |
19: 16,623,270 (GRCm39) |
N2797S |
possibly damaging |
Het |
Wscd2 |
T |
C |
5: 113,712,235 (GRCm39) |
Y385H |
probably damaging |
Het |
Xdh |
T |
C |
17: 74,229,500 (GRCm39) |
I318V |
probably benign |
Het |
Xrcc3 |
T |
A |
12: 111,774,313 (GRCm39) |
K172M |
probably damaging |
Het |
|
Other mutations in Or4a15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02134:Or4a15
|
APN |
2 |
89,193,172 (GRCm39) |
missense |
probably damaging |
0.97 |
R0945:Or4a15
|
UTSW |
2 |
89,193,599 (GRCm39) |
missense |
probably damaging |
0.98 |
R1018:Or4a15
|
UTSW |
2 |
89,193,523 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1419:Or4a15
|
UTSW |
2 |
89,193,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Or4a15
|
UTSW |
2 |
89,192,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Or4a15
|
UTSW |
2 |
89,193,353 (GRCm39) |
missense |
probably benign |
0.01 |
R2143:Or4a15
|
UTSW |
2 |
89,193,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R3499:Or4a15
|
UTSW |
2 |
89,193,294 (GRCm39) |
missense |
probably benign |
0.07 |
R3776:Or4a15
|
UTSW |
2 |
89,193,108 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4595:Or4a15
|
UTSW |
2 |
89,193,669 (GRCm39) |
missense |
probably damaging |
0.98 |
R6287:Or4a15
|
UTSW |
2 |
89,193,363 (GRCm39) |
nonsense |
probably null |
|
R7256:Or4a15
|
UTSW |
2 |
89,192,838 (GRCm39) |
missense |
probably benign |
0.21 |
R7516:Or4a15
|
UTSW |
2 |
89,193,719 (GRCm39) |
missense |
probably benign |
0.01 |
R7636:Or4a15
|
UTSW |
2 |
89,193,583 (GRCm39) |
nonsense |
probably null |
|
R7975:Or4a15
|
UTSW |
2 |
89,193,413 (GRCm39) |
missense |
probably benign |
0.23 |
R8240:Or4a15
|
UTSW |
2 |
89,192,896 (GRCm39) |
missense |
probably benign |
0.01 |
R8514:Or4a15
|
UTSW |
2 |
89,193,573 (GRCm39) |
missense |
probably benign |
0.06 |
R8780:Or4a15
|
UTSW |
2 |
89,193,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R8898:Or4a15
|
UTSW |
2 |
89,192,957 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9402:Or4a15
|
UTSW |
2 |
89,193,123 (GRCm39) |
nonsense |
probably null |
|
R9434:Or4a15
|
UTSW |
2 |
89,193,692 (GRCm39) |
missense |
probably benign |
0.02 |
R9451:Or4a15
|
UTSW |
2 |
89,193,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Or4a15
|
UTSW |
2 |
89,193,065 (GRCm39) |
missense |
probably damaging |
0.96 |
|