Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
T |
C |
12: 71,217,410 (GRCm39) |
V793A |
possibly damaging |
Het |
2900092C05Rik |
A |
G |
7: 12,246,599 (GRCm39) |
T32A |
probably benign |
Het |
Adprhl1 |
C |
T |
8: 13,274,977 (GRCm39) |
V594M |
possibly damaging |
Het |
Ano3 |
A |
T |
2: 110,496,220 (GRCm39) |
Y845N |
probably damaging |
Het |
Arhgap24 |
A |
T |
5: 103,040,778 (GRCm39) |
I575L |
probably benign |
Het |
Aurka |
A |
C |
2: 172,205,516 (GRCm39) |
|
probably null |
Het |
C1qtnf5 |
A |
T |
9: 44,020,267 (GRCm39) |
|
probably benign |
Het |
Cacnb2 |
A |
G |
2: 14,990,412 (GRCm39) |
D454G |
possibly damaging |
Het |
Chchd5 |
T |
C |
2: 128,972,437 (GRCm39) |
L87P |
probably damaging |
Het |
Col7a1 |
G |
T |
9: 108,793,671 (GRCm39) |
R1377L |
unknown |
Het |
Cpne8 |
A |
C |
15: 90,456,191 (GRCm39) |
S191A |
probably damaging |
Het |
Dhx30 |
A |
T |
9: 109,916,098 (GRCm39) |
I671N |
probably damaging |
Het |
Dnah12 |
A |
T |
14: 26,495,642 (GRCm39) |
K1423N |
possibly damaging |
Het |
Dnm3 |
T |
C |
1: 162,148,556 (GRCm39) |
M272V |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,037,411 (GRCm39) |
S3688C |
possibly damaging |
Het |
Frmpd1 |
A |
T |
4: 45,285,401 (GRCm39) |
L1407F |
probably damaging |
Het |
Fry |
T |
C |
5: 150,378,037 (GRCm39) |
S410P |
probably damaging |
Het |
Gm11565 |
T |
A |
11: 99,805,744 (GRCm39) |
C45* |
probably null |
Het |
Gngt1 |
A |
T |
6: 3,994,311 (GRCm39) |
R30* |
probably null |
Het |
Htt |
T |
C |
5: 35,064,430 (GRCm39) |
I2943T |
possibly damaging |
Het |
Kl |
T |
A |
5: 150,912,318 (GRCm39) |
M689K |
possibly damaging |
Het |
Lmo7 |
T |
A |
14: 102,137,573 (GRCm39) |
D247E |
probably benign |
Het |
Mastl |
G |
T |
2: 23,022,784 (GRCm39) |
N646K |
possibly damaging |
Het |
Mei4 |
G |
T |
9: 81,809,629 (GRCm39) |
L237F |
probably damaging |
Het |
Mettl27 |
C |
T |
5: 134,969,430 (GRCm39) |
P170S |
possibly damaging |
Het |
Mgam |
T |
A |
6: 40,734,648 (GRCm39) |
I896K |
probably damaging |
Het |
Mix23 |
T |
A |
16: 35,910,299 (GRCm39) |
V118D |
probably damaging |
Het |
Moxd1 |
T |
A |
10: 24,160,675 (GRCm39) |
C443S |
probably damaging |
Het |
Myo18b |
A |
T |
5: 113,022,038 (GRCm39) |
N451K |
probably benign |
Het |
Myo7b |
T |
C |
18: 32,121,602 (GRCm39) |
I768V |
probably benign |
Het |
Nos1 |
A |
C |
5: 118,005,639 (GRCm39) |
I120L |
probably benign |
Het |
Nsd1 |
T |
C |
13: 55,393,434 (GRCm39) |
V345A |
probably benign |
Het |
Or1j15 |
A |
T |
2: 36,459,128 (GRCm39) |
T173S |
probably benign |
Het |
Or2aj5 |
C |
A |
16: 19,424,675 (GRCm39) |
V248F |
probably damaging |
Het |
Or5t15 |
A |
G |
2: 86,681,859 (GRCm39) |
L61P |
possibly damaging |
Het |
Or8g50 |
C |
T |
9: 39,648,372 (GRCm39) |
T87I |
probably benign |
Het |
Pdzph1 |
T |
G |
17: 59,280,622 (GRCm39) |
Q553H |
probably damaging |
Het |
Piwil1 |
T |
A |
5: 128,824,940 (GRCm39) |
L546* |
probably null |
Het |
Pla2g4f |
T |
C |
2: 120,131,552 (GRCm39) |
T724A |
probably benign |
Het |
Ralgapa2 |
A |
T |
2: 146,266,596 (GRCm39) |
M660K |
possibly damaging |
Het |
Rgsl1 |
T |
C |
1: 153,679,767 (GRCm39) |
D103G |
possibly damaging |
Het |
Rnf186 |
A |
G |
4: 138,694,565 (GRCm39) |
D35G |
probably damaging |
Het |
Rock2 |
A |
G |
12: 17,004,919 (GRCm39) |
D424G |
probably benign |
Het |
Scg2 |
A |
T |
1: 79,413,117 (GRCm39) |
D495E |
probably damaging |
Het |
Slc39a2 |
G |
A |
14: 52,131,681 (GRCm39) |
|
probably null |
Het |
Snrnp48 |
T |
A |
13: 38,394,212 (GRCm39) |
Y100* |
probably null |
Het |
Spaca1 |
A |
G |
4: 34,029,176 (GRCm39) |
M99T |
probably damaging |
Het |
Specc1 |
T |
G |
11: 62,008,950 (GRCm39) |
F235L |
probably damaging |
Het |
St13 |
A |
T |
15: 81,283,802 (GRCm39) |
|
probably null |
Het |
Swap70 |
T |
A |
7: 109,869,230 (GRCm39) |
M341K |
probably damaging |
Het |
Synj2 |
A |
G |
17: 6,036,487 (GRCm39) |
D67G |
probably benign |
Het |
Tmem135 |
T |
A |
7: 88,805,652 (GRCm39) |
I251F |
probably benign |
Het |
Tmem87a |
A |
T |
2: 120,190,584 (GRCm39) |
|
probably null |
Het |
Tom1l2 |
C |
T |
11: 60,123,753 (GRCm39) |
D128N |
probably damaging |
Het |
Tpx2 |
C |
A |
2: 152,715,024 (GRCm39) |
H82N |
probably benign |
Het |
Trip12 |
A |
T |
1: 84,738,733 (GRCm39) |
C738S |
possibly damaging |
Het |
Ttyh1 |
A |
G |
7: 4,128,561 (GRCm39) |
T153A |
probably benign |
Het |
Utrn |
C |
T |
10: 12,566,566 (GRCm39) |
G1199S |
probably benign |
Het |
Vmn1r8 |
T |
A |
6: 57,013,274 (GRCm39) |
N108K |
probably benign |
Het |
Vmn2r63 |
T |
A |
7: 42,583,104 (GRCm39) |
D37V |
probably damaging |
Het |
Vwce |
C |
T |
19: 10,621,585 (GRCm39) |
R206C |
possibly damaging |
Het |
Wrn |
G |
T |
8: 33,809,200 (GRCm39) |
F265L |
probably damaging |
Het |
Zfp472 |
T |
A |
17: 33,197,363 (GRCm39) |
C479* |
probably null |
Het |
Zfp831 |
A |
T |
2: 174,485,651 (GRCm39) |
T109S |
possibly damaging |
Het |
Znfx1 |
G |
T |
2: 166,898,646 (GRCm39) |
Q93K |
probably benign |
Het |
|
Other mutations in Or4c11c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00923:Or4c11c
|
APN |
2 |
88,661,456 (GRCm39) |
splice site |
probably null |
|
IGL02079:Or4c11c
|
APN |
2 |
88,661,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02183:Or4c11c
|
APN |
2 |
88,662,372 (GRCm39) |
missense |
probably benign |
|
IGL02813:Or4c11c
|
APN |
2 |
88,661,495 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02839:Or4c11c
|
APN |
2 |
88,661,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02895:Or4c11c
|
APN |
2 |
88,661,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R0680:Or4c11c
|
UTSW |
2 |
88,662,124 (GRCm39) |
missense |
probably benign |
|
R2029:Or4c11c
|
UTSW |
2 |
88,661,749 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2095:Or4c11c
|
UTSW |
2 |
88,661,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R6216:Or4c11c
|
UTSW |
2 |
88,661,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R6240:Or4c11c
|
UTSW |
2 |
88,661,707 (GRCm39) |
missense |
probably benign |
0.22 |
R6377:Or4c11c
|
UTSW |
2 |
88,661,613 (GRCm39) |
nonsense |
probably null |
|
R6429:Or4c11c
|
UTSW |
2 |
88,661,869 (GRCm39) |
missense |
probably benign |
0.01 |
R6521:Or4c11c
|
UTSW |
2 |
88,661,700 (GRCm39) |
missense |
probably benign |
0.03 |
R7065:Or4c11c
|
UTSW |
2 |
88,661,730 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Or4c11c
|
UTSW |
2 |
88,662,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R7476:Or4c11c
|
UTSW |
2 |
88,661,932 (GRCm39) |
missense |
probably benign |
0.07 |
R7570:Or4c11c
|
UTSW |
2 |
88,661,472 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8303:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8306:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8307:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8308:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8344:Or4c11c
|
UTSW |
2 |
88,661,727 (GRCm39) |
missense |
probably benign |
0.00 |
R8386:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8387:Or4c11c
|
UTSW |
2 |
88,661,633 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8809:Or4c11c
|
UTSW |
2 |
88,662,256 (GRCm39) |
missense |
probably benign |
0.01 |
R8894:Or4c11c
|
UTSW |
2 |
88,661,809 (GRCm39) |
missense |
probably benign |
0.12 |
Z1176:Or4c11c
|
UTSW |
2 |
88,661,922 (GRCm39) |
missense |
probably damaging |
0.99 |
|