Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930553J12Rik |
T |
A |
16: 88,617,189 (GRCm39) |
C29* |
probably null |
Het |
Abca4 |
G |
A |
3: 121,877,613 (GRCm39) |
C324Y |
probably damaging |
Het |
Ablim2 |
T |
G |
5: 35,994,277 (GRCm39) |
|
probably benign |
Het |
Abr |
A |
T |
11: 76,369,870 (GRCm39) |
V115E |
probably damaging |
Het |
Adgrl2 |
C |
T |
3: 148,571,231 (GRCm39) |
|
probably null |
Het |
Aff3 |
A |
T |
1: 38,243,013 (GRCm39) |
S936T |
probably benign |
Het |
Agap3 |
T |
C |
5: 24,656,200 (GRCm39) |
|
probably benign |
Het |
Ahrr |
T |
A |
13: 74,362,705 (GRCm39) |
S393C |
probably damaging |
Het |
Amfr |
T |
C |
8: 94,713,998 (GRCm39) |
|
probably null |
Het |
Ankrd26 |
C |
A |
6: 118,484,598 (GRCm39) |
|
probably null |
Het |
Asxl3 |
G |
A |
18: 22,650,668 (GRCm39) |
V886I |
probably benign |
Het |
Atp5f1a |
C |
A |
18: 77,867,895 (GRCm39) |
N356K |
probably damaging |
Het |
AU021092 |
A |
T |
16: 5,040,031 (GRCm39) |
M31K |
possibly damaging |
Het |
Bicral |
A |
G |
17: 47,124,978 (GRCm39) |
|
probably benign |
Het |
Btbd9 |
C |
T |
17: 30,493,916 (GRCm39) |
D492N |
possibly damaging |
Het |
C3ar1 |
T |
C |
6: 122,827,731 (GRCm39) |
D162G |
probably benign |
Het |
Camkk2 |
C |
T |
5: 122,901,940 (GRCm39) |
C123Y |
probably benign |
Het |
Casp8ap2 |
A |
T |
4: 32,644,079 (GRCm39) |
I1051F |
probably damaging |
Het |
Catsperg1 |
A |
T |
7: 28,894,965 (GRCm39) |
V544E |
probably damaging |
Het |
Cdc27 |
G |
A |
11: 104,417,817 (GRCm39) |
|
probably benign |
Het |
Colec12 |
C |
T |
18: 9,858,921 (GRCm39) |
P568L |
unknown |
Het |
Dennd6b |
T |
C |
15: 89,080,432 (GRCm39) |
Q56R |
probably benign |
Het |
Dmac2l |
T |
C |
12: 69,787,663 (GRCm39) |
|
probably benign |
Het |
Fbxl17 |
G |
A |
17: 63,692,062 (GRCm39) |
|
probably benign |
Het |
Fubp1 |
T |
C |
3: 151,925,350 (GRCm39) |
V164A |
probably damaging |
Het |
Gdap2 |
G |
A |
3: 100,085,572 (GRCm39) |
G165S |
probably damaging |
Het |
Gns |
A |
G |
10: 121,219,328 (GRCm39) |
K352E |
probably benign |
Het |
Gtf2ird2 |
C |
T |
5: 134,220,088 (GRCm39) |
T22M |
probably damaging |
Het |
Herc3 |
A |
G |
6: 58,845,613 (GRCm39) |
|
probably benign |
Het |
Hp1bp3 |
C |
T |
4: 137,964,520 (GRCm39) |
S348F |
probably damaging |
Het |
Inpp1 |
A |
T |
1: 52,838,513 (GRCm39) |
F45L |
probably damaging |
Het |
Ipo4 |
T |
C |
14: 55,863,399 (GRCm39) |
Q1073R |
possibly damaging |
Het |
Itgae |
A |
G |
11: 73,008,973 (GRCm39) |
K485E |
probably benign |
Het |
Jak2 |
G |
A |
19: 29,261,029 (GRCm39) |
V342I |
probably damaging |
Het |
Kptn |
C |
A |
7: 15,859,666 (GRCm39) |
Q297K |
probably damaging |
Het |
Lims2 |
A |
G |
18: 32,077,573 (GRCm39) |
E103G |
probably benign |
Het |
Mthfr |
C |
G |
4: 148,139,885 (GRCm39) |
S618W |
probably damaging |
Het |
Nanos3 |
C |
T |
8: 84,902,763 (GRCm39) |
R133Q |
probably damaging |
Het |
Nup133 |
A |
G |
8: 124,644,185 (GRCm39) |
V727A |
possibly damaging |
Het |
Oas2 |
T |
G |
5: 120,881,152 (GRCm39) |
E313A |
probably damaging |
Het |
Or10d4c |
G |
A |
9: 39,558,646 (GRCm39) |
C208Y |
probably damaging |
Het |
Or52b2 |
C |
A |
7: 104,986,814 (GRCm39) |
M36I |
probably benign |
Het |
Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
Or5m8 |
T |
A |
2: 85,822,726 (GRCm39) |
C188* |
probably null |
Het |
Park7 |
A |
G |
4: 150,992,806 (GRCm39) |
V20A |
possibly damaging |
Het |
Pgap4 |
T |
C |
4: 49,586,566 (GRCm39) |
T201A |
probably benign |
Het |
Phldb1 |
C |
A |
9: 44,612,964 (GRCm39) |
V919L |
probably benign |
Het |
Pkhd1l1 |
C |
A |
15: 44,460,407 (GRCm39) |
H4205Q |
probably benign |
Het |
Plekhg3 |
G |
T |
12: 76,613,040 (GRCm39) |
E449* |
probably null |
Het |
Pramel26 |
A |
T |
4: 143,537,338 (GRCm39) |
I331N |
probably damaging |
Het |
Pstpip1 |
T |
C |
9: 56,033,929 (GRCm39) |
V301A |
probably benign |
Het |
Ptdss1 |
G |
A |
13: 67,081,636 (GRCm39) |
R22H |
probably damaging |
Het |
Ptprq |
A |
G |
10: 107,541,443 (GRCm39) |
V361A |
probably benign |
Het |
Ralgapa2 |
A |
T |
2: 146,188,714 (GRCm39) |
V1309E |
possibly damaging |
Het |
Rere |
T |
C |
4: 150,695,438 (GRCm39) |
|
probably benign |
Het |
Sbk3 |
T |
A |
7: 4,970,404 (GRCm39) |
T322S |
possibly damaging |
Het |
Scn9a |
T |
A |
2: 66,335,354 (GRCm39) |
I1203L |
probably damaging |
Het |
Setdb1 |
A |
T |
3: 95,233,442 (GRCm39) |
|
probably benign |
Het |
Sik3 |
C |
A |
9: 46,120,109 (GRCm39) |
Q683K |
probably damaging |
Het |
Slc24a5 |
A |
G |
2: 124,927,621 (GRCm39) |
I307V |
probably benign |
Het |
Smg6 |
A |
G |
11: 74,820,647 (GRCm39) |
D306G |
probably damaging |
Het |
Snx13 |
G |
A |
12: 35,136,899 (GRCm39) |
W120* |
probably null |
Het |
Snx5 |
A |
G |
2: 144,099,128 (GRCm39) |
|
probably benign |
Het |
Srsf5 |
T |
C |
12: 80,994,298 (GRCm39) |
S76P |
probably benign |
Het |
Stard6 |
A |
G |
18: 70,629,186 (GRCm39) |
D31G |
probably damaging |
Het |
Taf3 |
A |
G |
2: 9,956,709 (GRCm39) |
M333T |
probably benign |
Het |
Taf6 |
T |
G |
5: 138,179,409 (GRCm39) |
I377L |
probably benign |
Het |
Taf8 |
G |
T |
17: 47,804,505 (GRCm39) |
N252K |
probably benign |
Het |
Tfap2c |
A |
G |
2: 172,393,423 (GRCm39) |
T113A |
probably benign |
Het |
Tmtc4 |
C |
T |
14: 123,215,572 (GRCm39) |
V25M |
probably damaging |
Het |
Topbp1 |
T |
A |
9: 103,205,886 (GRCm39) |
D841E |
probably damaging |
Het |
Topbp1 |
T |
A |
9: 103,185,932 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,542,833 (GRCm39) |
D33384E |
probably damaging |
Het |
Unc13c |
T |
C |
9: 73,838,067 (GRCm39) |
E928G |
probably benign |
Het |
Vav1 |
T |
C |
17: 57,603,090 (GRCm39) |
F81L |
probably damaging |
Het |
Vmn2r63 |
A |
G |
7: 42,553,042 (GRCm39) |
I738T |
probably damaging |
Het |
Vmn2r87 |
C |
T |
10: 130,315,806 (GRCm39) |
E87K |
probably damaging |
Het |
Zfp229 |
A |
T |
17: 21,964,822 (GRCm39) |
M351L |
probably benign |
Het |
|
Other mutations in Or5p63 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01356:Or5p63
|
APN |
7 |
107,810,933 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03133:Or5p63
|
APN |
7 |
107,811,594 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03326:Or5p63
|
APN |
7 |
107,810,837 (GRCm39) |
missense |
probably benign |
0.03 |
R0141:Or5p63
|
UTSW |
7 |
107,811,210 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0595:Or5p63
|
UTSW |
7 |
107,810,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R1427:Or5p63
|
UTSW |
7 |
107,811,301 (GRCm39) |
missense |
probably benign |
0.07 |
R2023:Or5p63
|
UTSW |
7 |
107,811,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R2065:Or5p63
|
UTSW |
7 |
107,811,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R2068:Or5p63
|
UTSW |
7 |
107,811,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R3410:Or5p63
|
UTSW |
7 |
107,811,490 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4024:Or5p63
|
UTSW |
7 |
107,810,949 (GRCm39) |
nonsense |
probably null |
|
R4619:Or5p63
|
UTSW |
7 |
107,811,301 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4738:Or5p63
|
UTSW |
7 |
107,811,201 (GRCm39) |
missense |
probably damaging |
0.99 |
R5004:Or5p63
|
UTSW |
7 |
107,811,323 (GRCm39) |
nonsense |
probably null |
|
R5684:Or5p63
|
UTSW |
7 |
107,811,279 (GRCm39) |
nonsense |
probably null |
|
R6782:Or5p63
|
UTSW |
7 |
107,811,670 (GRCm39) |
missense |
probably benign |
0.03 |
R6889:Or5p63
|
UTSW |
7 |
107,811,125 (GRCm39) |
missense |
probably benign |
0.00 |
R7010:Or5p63
|
UTSW |
7 |
107,811,349 (GRCm39) |
missense |
probably damaging |
0.98 |
R7076:Or5p63
|
UTSW |
7 |
107,811,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R8162:Or5p63
|
UTSW |
7 |
107,810,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R8190:Or5p63
|
UTSW |
7 |
107,811,014 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9108:Or5p63
|
UTSW |
7 |
107,810,846 (GRCm39) |
missense |
probably damaging |
1.00 |
R9172:Or5p63
|
UTSW |
7 |
107,811,169 (GRCm39) |
missense |
probably benign |
0.12 |
Z1177:Or5p63
|
UTSW |
7 |
107,811,176 (GRCm39) |
missense |
probably benign |
|
|