Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810021J22Rik |
T |
A |
11: 58,770,966 (GRCm39) |
D149E |
probably benign |
Het |
Aars2 |
T |
C |
17: 45,818,523 (GRCm39) |
C103R |
probably damaging |
Het |
Aass |
T |
C |
6: 23,092,367 (GRCm39) |
D591G |
probably benign |
Het |
Arhgap32 |
A |
G |
9: 32,172,205 (GRCm39) |
T1662A |
probably benign |
Het |
Arhgap42 |
A |
T |
9: 9,009,327 (GRCm39) |
I520N |
probably damaging |
Het |
Arhgef3 |
T |
C |
14: 27,116,095 (GRCm39) |
I279T |
probably damaging |
Het |
Arid4b |
A |
G |
13: 14,294,808 (GRCm39) |
K30R |
probably damaging |
Het |
Asxl3 |
C |
T |
18: 22,657,473 (GRCm39) |
R1828W |
probably benign |
Het |
Bid |
T |
C |
6: 120,877,200 (GRCm39) |
Y47C |
probably benign |
Het |
Card6 |
T |
C |
15: 5,134,847 (GRCm39) |
T119A |
probably benign |
Het |
Cbr1 |
T |
C |
16: 93,406,905 (GRCm39) |
I207T |
probably damaging |
Het |
Cep135 |
T |
C |
5: 76,759,575 (GRCm39) |
L443P |
probably damaging |
Het |
Cfap251 |
T |
A |
5: 123,460,650 (GRCm39) |
V1204E |
probably damaging |
Het |
Cfap43 |
T |
A |
19: 47,754,274 (GRCm39) |
R1017* |
probably null |
Het |
Cfap52 |
T |
A |
11: 67,830,621 (GRCm39) |
S280C |
probably benign |
Het |
Cntnap5b |
T |
C |
1: 100,069,022 (GRCm39) |
F81L |
probably damaging |
Het |
Cyp4a12a |
A |
G |
4: 115,186,130 (GRCm39) |
D430G |
probably damaging |
Het |
Cyp4f37 |
G |
A |
17: 32,853,152 (GRCm39) |
|
probably null |
Het |
Dclre1a |
A |
G |
19: 56,531,121 (GRCm39) |
S742P |
probably damaging |
Het |
Ddx54 |
T |
C |
5: 120,759,855 (GRCm39) |
F414S |
probably damaging |
Het |
Dsp |
A |
G |
13: 38,381,319 (GRCm39) |
N2688S |
probably benign |
Het |
Elovl4 |
A |
T |
9: 83,670,320 (GRCm39) |
|
probably null |
Het |
Erbin |
A |
C |
13: 103,966,694 (GRCm39) |
|
probably null |
Het |
Fsip2 |
A |
G |
2: 82,818,724 (GRCm39) |
D4819G |
probably benign |
Het |
Gapvd1 |
G |
A |
2: 34,602,212 (GRCm39) |
P645L |
probably damaging |
Het |
Gbp9 |
T |
C |
5: 105,229,171 (GRCm39) |
E492G |
possibly damaging |
Het |
Gpc5 |
T |
A |
14: 115,665,667 (GRCm39) |
I497K |
probably benign |
Het |
Hlx |
A |
G |
1: 184,459,905 (GRCm39) |
L411P |
probably damaging |
Het |
Hmmr |
G |
A |
11: 40,612,499 (GRCm39) |
S206F |
probably damaging |
Het |
Ice1 |
A |
T |
13: 70,754,526 (GRCm39) |
I520N |
probably benign |
Het |
Ist1 |
T |
C |
8: 110,410,412 (GRCm39) |
|
probably null |
Het |
Itga3 |
T |
C |
11: 94,953,466 (GRCm39) |
D292G |
probably benign |
Het |
Kif21a |
T |
C |
15: 90,855,399 (GRCm39) |
N655S |
probably damaging |
Het |
Lrrtm1 |
A |
G |
6: 77,221,662 (GRCm39) |
H373R |
probably benign |
Het |
Ngdn |
A |
T |
14: 55,260,602 (GRCm39) |
H270L |
probably benign |
Het |
Nol4 |
G |
A |
18: 23,173,231 (GRCm39) |
|
probably benign |
Het |
Nup50l |
T |
C |
6: 96,142,702 (GRCm39) |
E114G |
probably benign |
Het |
Nxpe5 |
G |
A |
5: 138,239,264 (GRCm39) |
|
probably benign |
Het |
Or1j18 |
A |
G |
2: 36,624,467 (GRCm39) |
I45V |
probably damaging |
Het |
Or8d1 |
A |
C |
9: 38,766,837 (GRCm39) |
T160P |
probably damaging |
Het |
Or8g30 |
A |
C |
9: 39,230,689 (GRCm39) |
S74A |
probably damaging |
Het |
Pask |
C |
A |
1: 93,248,286 (GRCm39) |
R1005L |
probably benign |
Het |
Pcm1 |
A |
G |
8: 41,736,758 (GRCm39) |
T875A |
probably damaging |
Het |
Pdrg1 |
A |
T |
2: 152,851,587 (GRCm39) |
I130N |
probably damaging |
Het |
Plec |
A |
T |
15: 76,073,466 (GRCm39) |
M448K |
unknown |
Het |
R3hdml |
T |
G |
2: 163,341,832 (GRCm39) |
V204G |
probably damaging |
Het |
Rasa4 |
G |
A |
5: 136,118,235 (GRCm39) |
V32M |
possibly damaging |
Het |
Scaf8 |
T |
C |
17: 3,198,827 (GRCm39) |
V44A |
unknown |
Het |
Smad3 |
G |
T |
9: 63,574,760 (GRCm39) |
P177T |
probably benign |
Het |
Smpd4 |
T |
A |
16: 17,457,195 (GRCm39) |
F384L |
probably damaging |
Het |
Sycp2l |
G |
C |
13: 41,283,275 (GRCm39) |
L170F |
probably damaging |
Het |
Tas2r107 |
T |
C |
6: 131,636,585 (GRCm39) |
S155G |
probably benign |
Het |
Tmem143 |
T |
A |
7: 45,565,994 (GRCm39) |
M439K |
probably benign |
Het |
Ttc41 |
A |
T |
10: 86,555,494 (GRCm39) |
T317S |
probably benign |
Het |
Umps |
A |
G |
16: 33,784,240 (GRCm39) |
V71A |
possibly damaging |
Het |
Usp17lc |
G |
A |
7: 103,067,389 (GRCm39) |
G228D |
possibly damaging |
Het |
Usp17ld |
C |
T |
7: 102,900,023 (GRCm39) |
C303Y |
probably damaging |
Het |
Vmn2r65 |
C |
A |
7: 84,589,391 (GRCm39) |
E842* |
probably null |
Het |
Vmn2r94 |
A |
G |
17: 18,464,433 (GRCm39) |
F619S |
probably damaging |
Het |
Vps13a |
T |
C |
19: 16,594,270 (GRCm39) |
T3154A |
probably benign |
Het |
Vps13b |
C |
T |
15: 35,640,063 (GRCm39) |
T1311I |
probably damaging |
Het |
Xpot |
A |
T |
10: 121,447,405 (GRCm39) |
Y353* |
probably null |
Het |
Zfp319 |
A |
T |
8: 96,055,765 (GRCm39) |
L146Q |
probably damaging |
Het |
Zfp422 |
T |
A |
6: 116,603,612 (GRCm39) |
H129L |
probably damaging |
Het |
Zzef1 |
T |
C |
11: 72,808,015 (GRCm39) |
F2709L |
probably damaging |
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 |
R6158:Or4c11c
|
UTSW |
2 |
88,661,490 (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 |
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 |
|