Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acads |
T |
C |
5: 115,251,226 (GRCm39) |
E86G |
probably benign |
Het |
Agmo |
A |
G |
12: 37,448,728 (GRCm39) |
T217A |
probably damaging |
Het |
Arhgap39 |
A |
G |
15: 76,621,702 (GRCm39) |
S300P |
probably benign |
Het |
Casp12 |
T |
C |
9: 5,346,647 (GRCm39) |
L58P |
probably damaging |
Het |
Ccar2 |
T |
C |
14: 70,389,902 (GRCm39) |
T24A |
probably benign |
Het |
Ccndbp1 |
C |
A |
2: 120,845,046 (GRCm39) |
T321K |
unknown |
Het |
Cd200r3 |
G |
A |
16: 44,774,503 (GRCm39) |
C172Y |
probably damaging |
Het |
Chd2 |
T |
A |
7: 73,187,132 (GRCm39) |
H9L |
probably benign |
Het |
Cracdl |
C |
A |
1: 37,663,010 (GRCm39) |
E963* |
probably null |
Het |
Cramp1 |
T |
A |
17: 25,201,674 (GRCm39) |
S603C |
probably damaging |
Het |
Csmd2 |
A |
T |
4: 128,287,331 (GRCm39) |
Y1022F |
|
Het |
Ctns |
T |
C |
11: 73,075,760 (GRCm39) |
Y363C |
probably damaging |
Het |
D630044L22Rik |
A |
G |
17: 26,179,118 (GRCm39) |
T15A |
possibly damaging |
Het |
Dhx38 |
A |
C |
8: 110,285,333 (GRCm39) |
I444M |
probably benign |
Het |
Dnah14 |
A |
T |
1: 181,443,459 (GRCm39) |
I450F |
possibly damaging |
Het |
Dpf1 |
T |
C |
7: 29,013,566 (GRCm39) |
F245L |
probably benign |
Het |
Efr3b |
A |
G |
12: 4,032,898 (GRCm39) |
V269A |
probably benign |
Het |
Eprs1 |
G |
T |
1: 185,126,653 (GRCm39) |
V530L |
possibly damaging |
Het |
Eps8l2 |
A |
G |
7: 140,922,860 (GRCm39) |
N41S |
probably damaging |
Het |
Erbb4 |
T |
C |
1: 68,435,470 (GRCm39) |
I142M |
probably damaging |
Het |
Fhip1a |
T |
C |
3: 85,637,868 (GRCm39) |
M144V |
probably damaging |
Het |
Flnc |
A |
T |
6: 29,457,445 (GRCm39) |
D2381V |
probably damaging |
Het |
Fndc1 |
T |
A |
17: 7,991,362 (GRCm39) |
D778V |
unknown |
Het |
Galnt3 |
A |
G |
2: 65,921,555 (GRCm39) |
I492T |
probably benign |
Het |
Gigyf2 |
T |
C |
1: 87,374,155 (GRCm39) |
M1261T |
probably damaging |
Het |
Haus8 |
A |
G |
8: 71,708,695 (GRCm39) |
F126S |
probably benign |
Het |
Hif3a |
A |
G |
7: 16,782,686 (GRCm39) |
L293S |
probably damaging |
Het |
Ino80c |
G |
A |
18: 24,239,707 (GRCm39) |
T200I |
unknown |
Het |
Jag1 |
T |
A |
2: 136,943,717 (GRCm39) |
M160L |
probably benign |
Het |
Kcnj12 |
C |
A |
11: 60,960,825 (GRCm39) |
H374Q |
probably damaging |
Het |
Lrrc27 |
A |
G |
7: 138,816,902 (GRCm39) |
I433M |
probably benign |
Het |
Lyzl4 |
C |
T |
9: 121,407,160 (GRCm39) |
W123* |
probably null |
Het |
Map2k4 |
A |
T |
11: 65,597,827 (GRCm39) |
C264S |
|
Het |
Mmrn1 |
C |
T |
6: 60,921,508 (GRCm39) |
|
probably benign |
Het |
Mug1 |
C |
T |
6: 121,850,631 (GRCm39) |
T709I |
probably benign |
Het |
Myo9a |
T |
A |
9: 59,781,931 (GRCm39) |
W1706R |
probably benign |
Het |
Nlrp5 |
A |
G |
7: 23,117,869 (GRCm39) |
E531G |
probably damaging |
Het |
Nrp2 |
C |
T |
1: 62,784,567 (GRCm39) |
R239C |
probably damaging |
Het |
Pcdhb11 |
A |
C |
18: 37,555,422 (GRCm39) |
I251L |
probably benign |
Het |
Per3 |
A |
G |
4: 151,113,270 (GRCm39) |
S353P |
probably damaging |
Het |
Piezo1 |
T |
C |
8: 123,213,750 (GRCm39) |
E1738G |
probably null |
Het |
Prr14l |
T |
C |
5: 32,988,508 (GRCm39) |
D329G |
probably benign |
Het |
Ptpn23 |
G |
T |
9: 110,217,267 (GRCm39) |
P863Q |
probably damaging |
Het |
Ptpn23 |
G |
T |
9: 110,217,268 (GRCm39) |
P863T |
possibly damaging |
Het |
Ptprq |
T |
C |
10: 107,479,896 (GRCm39) |
K1125E |
possibly damaging |
Het |
Rapgef2 |
T |
G |
3: 79,000,343 (GRCm39) |
T351P |
probably damaging |
Het |
Rbl2 |
A |
G |
8: 91,840,617 (GRCm39) |
Y923C |
probably damaging |
Het |
Rimbp3 |
T |
C |
16: 17,028,727 (GRCm39) |
V717A |
probably benign |
Het |
Rims1 |
C |
T |
1: 22,358,760 (GRCm39) |
W182* |
probably null |
Het |
Rnmt |
A |
G |
18: 68,440,723 (GRCm39) |
K129E |
probably benign |
Het |
Ruvbl1 |
T |
C |
6: 88,450,108 (GRCm39) |
F93S |
probably damaging |
Het |
Scamp5 |
T |
C |
9: 57,350,969 (GRCm39) |
Y231C |
probably damaging |
Het |
Sfxn5 |
T |
A |
6: 85,244,921 (GRCm39) |
|
probably null |
Het |
Skic2 |
A |
T |
17: 35,068,975 (GRCm39) |
V8D |
probably benign |
Het |
Slc12a1 |
T |
C |
2: 125,028,234 (GRCm39) |
F510S |
probably damaging |
Het |
Sowahb |
T |
C |
5: 93,190,922 (GRCm39) |
Y599C |
probably damaging |
Het |
Speer4e1 |
T |
C |
5: 14,987,111 (GRCm39) |
N98S |
probably damaging |
Het |
Stat3 |
T |
C |
11: 100,784,807 (GRCm39) |
N553S |
probably benign |
Het |
Sult6b2 |
A |
T |
6: 142,735,868 (GRCm39) |
L242Q |
probably damaging |
Het |
Tacc3 |
C |
T |
5: 33,821,169 (GRCm39) |
R98W |
possibly damaging |
Het |
Tuba4a |
C |
T |
1: 75,193,595 (GRCm39) |
R112H |
|
Het |
Ubr3 |
T |
A |
2: 69,819,220 (GRCm39) |
S1337T |
probably damaging |
Het |
Vmn2r69 |
A |
T |
7: 85,055,713 (GRCm39) |
C808* |
probably null |
Het |
Wnt16 |
G |
A |
6: 22,288,997 (GRCm39) |
A105T |
probably benign |
Het |
Zfp692 |
C |
T |
11: 58,198,560 (GRCm39) |
S50L |
probably damaging |
Het |
|
Other mutations in Crtac1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00942:Crtac1
|
APN |
19 |
42,312,233 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01296:Crtac1
|
APN |
19 |
42,272,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01991:Crtac1
|
APN |
19 |
42,402,560 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02811:Crtac1
|
APN |
19 |
42,322,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Crtac1
|
UTSW |
19 |
42,276,383 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2046:Crtac1
|
UTSW |
19 |
42,322,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Crtac1
|
UTSW |
19 |
42,312,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R2280:Crtac1
|
UTSW |
19 |
42,272,006 (GRCm39) |
missense |
unknown |
|
R2281:Crtac1
|
UTSW |
19 |
42,272,006 (GRCm39) |
missense |
unknown |
|
R3508:Crtac1
|
UTSW |
19 |
42,293,180 (GRCm39) |
missense |
probably benign |
0.09 |
R3923:Crtac1
|
UTSW |
19 |
42,322,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R4072:Crtac1
|
UTSW |
19 |
42,293,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Crtac1
|
UTSW |
19 |
42,312,240 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4951:Crtac1
|
UTSW |
19 |
42,402,570 (GRCm39) |
missense |
probably benign |
|
R4965:Crtac1
|
UTSW |
19 |
42,307,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R5190:Crtac1
|
UTSW |
19 |
42,322,347 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5579:Crtac1
|
UTSW |
19 |
42,293,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R5595:Crtac1
|
UTSW |
19 |
42,402,390 (GRCm39) |
missense |
probably benign |
0.08 |
R5739:Crtac1
|
UTSW |
19 |
42,290,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Crtac1
|
UTSW |
19 |
42,297,629 (GRCm39) |
splice site |
probably null |
|
R5936:Crtac1
|
UTSW |
19 |
42,312,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R6149:Crtac1
|
UTSW |
19 |
42,272,048 (GRCm39) |
missense |
unknown |
|
R6193:Crtac1
|
UTSW |
19 |
42,312,236 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6858:Crtac1
|
UTSW |
19 |
42,307,174 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7246:Crtac1
|
UTSW |
19 |
42,276,365 (GRCm39) |
missense |
probably benign |
|
R7726:Crtac1
|
UTSW |
19 |
42,290,690 (GRCm39) |
nonsense |
probably null |
|
R7991:Crtac1
|
UTSW |
19 |
42,322,399 (GRCm39) |
missense |
probably benign |
0.24 |
R8046:Crtac1
|
UTSW |
19 |
42,297,492 (GRCm39) |
splice site |
probably benign |
|
R8350:Crtac1
|
UTSW |
19 |
42,297,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R8450:Crtac1
|
UTSW |
19 |
42,297,625 (GRCm39) |
missense |
probably damaging |
1.00 |
R9756:Crtac1
|
UTSW |
19 |
42,286,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R9766:Crtac1
|
UTSW |
19 |
42,402,557 (GRCm39) |
missense |
possibly damaging |
0.96 |
X0018:Crtac1
|
UTSW |
19 |
42,297,553 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Crtac1
|
UTSW |
19 |
42,276,365 (GRCm39) |
missense |
probably benign |
|
|