Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730049H05Rik |
T |
C |
6: 92,808,967 (GRCm39) |
V98A |
unknown |
Het |
Abca15 |
A |
T |
7: 119,987,439 (GRCm39) |
M1242L |
probably benign |
Het |
Abcb9 |
G |
A |
5: 124,214,090 (GRCm39) |
R576C |
possibly damaging |
Het |
Abl2 |
A |
G |
1: 156,452,902 (GRCm39) |
S146G |
probably damaging |
Het |
Aga |
G |
A |
8: 53,966,627 (GRCm39) |
G60S |
probably damaging |
Het |
Amigo1 |
T |
A |
3: 108,095,944 (GRCm39) |
V481D |
probably damaging |
Het |
Ano5 |
C |
A |
7: 51,243,415 (GRCm39) |
P846Q |
probably damaging |
Het |
Ccdc62 |
C |
A |
5: 124,092,470 (GRCm39) |
T485K |
probably benign |
Het |
Cd177 |
A |
T |
7: 24,445,550 (GRCm39) |
I631K |
possibly damaging |
Het |
Chil6 |
T |
A |
3: 106,313,411 (GRCm39) |
|
probably benign |
Het |
Clip1 |
A |
G |
5: 123,717,441 (GRCm39) |
S1283P |
probably damaging |
Het |
Dcbld1 |
T |
A |
10: 52,138,028 (GRCm39) |
D97E |
probably benign |
Het |
Decr1 |
G |
A |
4: 15,930,969 (GRCm39) |
P121L |
probably damaging |
Het |
Ehmt1 |
A |
T |
2: 24,729,578 (GRCm39) |
L661Q |
probably benign |
Het |
Eif2d |
A |
G |
1: 131,085,972 (GRCm39) |
M156V |
possibly damaging |
Het |
Ermn |
A |
T |
2: 57,938,010 (GRCm39) |
I201K |
probably damaging |
Het |
Etfbkmt |
T |
C |
6: 149,045,663 (GRCm39) |
C6R |
probably benign |
Het |
Evx2 |
A |
T |
2: 74,488,109 (GRCm39) |
|
probably null |
Het |
Fam222a |
T |
C |
5: 114,748,905 (GRCm39) |
S34P |
probably benign |
Het |
Fmo6 |
A |
T |
1: 162,748,046 (GRCm39) |
D339E |
probably benign |
Het |
Fubp1 |
T |
C |
3: 151,923,873 (GRCm39) |
S142P |
probably benign |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,450 (GRCm39) |
|
probably benign |
Het |
Gnb1 |
A |
T |
4: 155,625,033 (GRCm39) |
Q75L |
probably damaging |
Het |
Gucy2e |
C |
T |
11: 69,126,778 (GRCm39) |
A232T |
possibly damaging |
Het |
Haspin |
A |
T |
11: 73,026,936 (GRCm39) |
C718S |
probably benign |
Het |
Iqcd |
C |
T |
5: 120,738,707 (GRCm39) |
P175L |
possibly damaging |
Het |
Jph1 |
T |
A |
1: 17,167,632 (GRCm39) |
Q66L |
probably benign |
Het |
Kank1 |
G |
T |
19: 25,386,944 (GRCm39) |
D206Y |
possibly damaging |
Het |
Klf14 |
T |
C |
6: 30,935,470 (GRCm39) |
T55A |
probably benign |
Het |
Lclat1 |
T |
C |
17: 73,494,879 (GRCm39) |
M125T |
probably damaging |
Het |
Lgr5 |
T |
A |
10: 115,423,349 (GRCm39) |
Q17L |
probably benign |
Het |
Lrmda |
A |
G |
14: 22,648,361 (GRCm39) |
I64V |
unknown |
Het |
Lrrc15 |
A |
G |
16: 30,092,415 (GRCm39) |
L308P |
probably damaging |
Het |
Lyst |
C |
A |
13: 13,871,245 (GRCm39) |
Q2661K |
probably benign |
Het |
Map3k21 |
T |
A |
8: 126,638,027 (GRCm39) |
D204E |
possibly damaging |
Het |
Msln |
T |
C |
17: 25,970,125 (GRCm39) |
I277V |
probably benign |
Het |
Ndst4 |
C |
T |
3: 125,518,385 (GRCm39) |
S354L |
probably benign |
Het |
Nup153 |
G |
A |
13: 46,835,138 (GRCm39) |
T1389M |
probably damaging |
Het |
Or8c10 |
A |
G |
9: 38,279,268 (GRCm39) |
Y132C |
probably damaging |
Het |
Plcd1 |
T |
C |
9: 118,901,723 (GRCm39) |
|
probably null |
Het |
Plce1 |
C |
T |
19: 38,748,551 (GRCm39) |
R1761C |
probably damaging |
Het |
Prrc2b |
T |
C |
2: 32,103,414 (GRCm39) |
L964P |
probably damaging |
Het |
Prss43 |
T |
C |
9: 110,656,564 (GRCm39) |
S84P |
possibly damaging |
Het |
Rffl |
T |
C |
11: 82,703,633 (GRCm39) |
T97A |
possibly damaging |
Het |
Riok2 |
G |
C |
17: 17,598,057 (GRCm39) |
G48A |
possibly damaging |
Het |
Sec24a |
A |
G |
11: 51,617,331 (GRCm39) |
M488T |
probably benign |
Het |
Setdb2 |
C |
T |
14: 59,646,881 (GRCm39) |
D545N |
possibly damaging |
Het |
Slc39a4 |
T |
A |
15: 76,498,126 (GRCm39) |
H400L |
possibly damaging |
Het |
St7 |
T |
A |
6: 17,846,271 (GRCm39) |
F175I |
probably damaging |
Het |
Syne1 |
T |
A |
10: 5,299,324 (GRCm39) |
D977V |
probably damaging |
Het |
Tenm4 |
C |
T |
7: 96,534,646 (GRCm39) |
T1801I |
probably damaging |
Het |
Terf1 |
C |
T |
1: 15,883,295 (GRCm39) |
T136I |
probably damaging |
Het |
Tnnt1 |
T |
C |
7: 4,513,381 (GRCm39) |
S42G |
probably benign |
Het |
Trappc8 |
A |
G |
18: 21,000,822 (GRCm39) |
V287A |
probably benign |
Het |
Ttc3 |
T |
A |
16: 94,230,467 (GRCm39) |
I870K |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,574,389 (GRCm39) |
N25501K |
possibly damaging |
Het |
Unc13c |
A |
T |
9: 73,485,715 (GRCm39) |
W1662R |
probably damaging |
Het |
Wdr47 |
T |
A |
3: 108,525,890 (GRCm39) |
C138S |
probably damaging |
Het |
Zfp458 |
A |
G |
13: 67,408,298 (GRCm39) |
S6P |
probably damaging |
Het |
Zfp668 |
A |
C |
7: 127,465,804 (GRCm39) |
L460* |
probably null |
Het |
|
Other mutations in Cpt1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00785:Cpt1a
|
APN |
19 |
3,416,389 (GRCm39) |
missense |
possibly damaging |
0.85 |
allosouris
|
UTSW |
19 |
3,428,472 (GRCm39) |
missense |
probably damaging |
1.00 |
Tyrannosouris
|
UTSW |
19 |
3,412,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0029:Cpt1a
|
UTSW |
19 |
3,431,674 (GRCm39) |
missense |
probably benign |
0.04 |
R0029:Cpt1a
|
UTSW |
19 |
3,431,674 (GRCm39) |
missense |
probably benign |
0.04 |
R0305:Cpt1a
|
UTSW |
19 |
3,428,455 (GRCm39) |
missense |
probably benign |
|
R0963:Cpt1a
|
UTSW |
19 |
3,431,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Cpt1a
|
UTSW |
19 |
3,415,788 (GRCm39) |
splice site |
probably benign |
|
R2102:Cpt1a
|
UTSW |
19 |
3,421,585 (GRCm39) |
missense |
probably benign |
0.25 |
R3034:Cpt1a
|
UTSW |
19 |
3,428,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R3153:Cpt1a
|
UTSW |
19 |
3,406,430 (GRCm39) |
missense |
probably damaging |
0.99 |
R5195:Cpt1a
|
UTSW |
19 |
3,433,800 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5391:Cpt1a
|
UTSW |
19 |
3,399,260 (GRCm39) |
missense |
probably damaging |
0.98 |
R5964:Cpt1a
|
UTSW |
19 |
3,415,760 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6031:Cpt1a
|
UTSW |
19 |
3,421,556 (GRCm39) |
splice site |
probably null |
|
R6031:Cpt1a
|
UTSW |
19 |
3,421,556 (GRCm39) |
splice site |
probably null |
|
R6246:Cpt1a
|
UTSW |
19 |
3,426,550 (GRCm39) |
missense |
probably damaging |
0.99 |
R6339:Cpt1a
|
UTSW |
19 |
3,412,152 (GRCm39) |
missense |
probably benign |
0.27 |
R6427:Cpt1a
|
UTSW |
19 |
3,412,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R6535:Cpt1a
|
UTSW |
19 |
3,415,788 (GRCm39) |
splice site |
probably null |
|
R6621:Cpt1a
|
UTSW |
19 |
3,428,472 (GRCm39) |
missense |
probably damaging |
1.00 |
R6892:Cpt1a
|
UTSW |
19 |
3,421,660 (GRCm39) |
missense |
probably benign |
0.00 |
R7142:Cpt1a
|
UTSW |
19 |
3,425,100 (GRCm39) |
missense |
probably benign |
0.00 |
R7385:Cpt1a
|
UTSW |
19 |
3,430,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R7908:Cpt1a
|
UTSW |
19 |
3,412,202 (GRCm39) |
missense |
probably benign |
0.26 |
R8098:Cpt1a
|
UTSW |
19 |
3,420,849 (GRCm39) |
missense |
probably benign |
|
R8362:Cpt1a
|
UTSW |
19 |
3,420,744 (GRCm39) |
nonsense |
probably null |
|
R8444:Cpt1a
|
UTSW |
19 |
3,431,981 (GRCm39) |
missense |
probably benign |
|
R8854:Cpt1a
|
UTSW |
19 |
3,406,327 (GRCm39) |
missense |
probably benign |
0.00 |
R8918:Cpt1a
|
UTSW |
19 |
3,408,258 (GRCm39) |
missense |
|
|
R8951:Cpt1a
|
UTSW |
19 |
3,412,211 (GRCm39) |
missense |
probably benign |
0.14 |
R9295:Cpt1a
|
UTSW |
19 |
3,428,441 (GRCm39) |
missense |
probably damaging |
0.99 |
R9495:Cpt1a
|
UTSW |
19 |
3,433,795 (GRCm39) |
missense |
probably benign |
|
R9560:Cpt1a
|
UTSW |
19 |
3,402,531 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9735:Cpt1a
|
UTSW |
19 |
3,420,825 (GRCm39) |
missense |
probably benign |
|
X0019:Cpt1a
|
UTSW |
19 |
3,416,348 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Cpt1a
|
UTSW |
19 |
3,420,727 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cpt1a
|
UTSW |
19 |
3,416,370 (GRCm39) |
missense |
probably damaging |
1.00 |
|