Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
T |
C |
9: 57,164,832 (GRCm39) |
D514G |
probably damaging |
Het |
Acbd7 |
A |
T |
2: 3,341,478 (GRCm39) |
I41F |
possibly damaging |
Het |
Actr8 |
G |
T |
14: 29,709,181 (GRCm39) |
V262L |
probably benign |
Het |
Anp32e |
A |
G |
3: 95,844,454 (GRCm39) |
D108G |
probably damaging |
Het |
Banp |
G |
A |
8: 122,747,294 (GRCm39) |
G448S |
probably benign |
Het |
Camsap3 |
G |
A |
8: 3,637,960 (GRCm39) |
|
probably null |
Het |
Cd22 |
C |
A |
7: 30,568,934 (GRCm39) |
|
probably null |
Het |
Cfap58 |
A |
T |
19: 47,951,001 (GRCm39) |
Q454L |
probably damaging |
Het |
Cntn4 |
C |
T |
6: 106,632,542 (GRCm39) |
T522I |
probably benign |
Het |
Col11a1 |
G |
A |
3: 113,883,829 (GRCm39) |
D233N |
unknown |
Het |
Csmd1 |
G |
T |
8: 16,083,590 (GRCm39) |
|
probably null |
Het |
Csmd3 |
T |
A |
15: 47,840,429 (GRCm39) |
Y946F |
probably damaging |
Het |
D5Ertd579e |
G |
T |
5: 36,830,210 (GRCm39) |
P38Q |
probably damaging |
Het |
Dnal4 |
T |
C |
15: 79,646,226 (GRCm39) |
T93A |
probably benign |
Het |
Dsp |
A |
T |
13: 38,367,194 (GRCm39) |
D614V |
probably damaging |
Het |
Fcgr1 |
A |
T |
3: 96,199,682 (GRCm39) |
I75N |
possibly damaging |
Het |
Fgd6 |
T |
A |
10: 93,970,909 (GRCm39) |
Y1229N |
probably benign |
Het |
Fhip2a |
G |
A |
19: 57,369,522 (GRCm39) |
A383T |
probably damaging |
Het |
Frmpd1 |
T |
G |
4: 45,268,497 (GRCm39) |
L214R |
probably damaging |
Het |
Gapvd1 |
A |
T |
2: 34,602,337 (GRCm39) |
D603E |
probably damaging |
Het |
H2-M9 |
A |
G |
17: 36,952,665 (GRCm39) |
V127A |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,782,296 (GRCm39) |
S1328T |
possibly damaging |
Het |
Ica1l |
T |
C |
1: 60,045,456 (GRCm39) |
N269S |
probably benign |
Het |
Il18r1 |
T |
C |
1: 40,526,188 (GRCm39) |
Y245H |
probably damaging |
Het |
Il6ra |
A |
T |
3: 89,794,376 (GRCm39) |
V195E |
probably damaging |
Het |
Inpp5j |
A |
G |
11: 3,451,439 (GRCm39) |
|
probably benign |
Het |
Isy1 |
T |
C |
6: 87,796,125 (GRCm39) |
T271A |
probably benign |
Het |
Klra9 |
T |
C |
6: 130,155,993 (GRCm39) |
Y254C |
probably damaging |
Het |
Ly6e |
T |
G |
15: 74,830,219 (GRCm39) |
S73A |
probably damaging |
Het |
Muc4 |
G |
A |
16: 32,576,570 (GRCm39) |
|
probably benign |
Het |
Myh3 |
A |
G |
11: 66,981,340 (GRCm39) |
|
probably null |
Het |
Ndor1 |
G |
A |
2: 25,138,360 (GRCm39) |
H409Y |
probably benign |
Het |
Nwd2 |
A |
G |
5: 63,965,234 (GRCm39) |
D1606G |
probably damaging |
Het |
Or2t44 |
A |
G |
11: 58,677,935 (GRCm39) |
N292D |
probably damaging |
Het |
Or3a1d |
G |
A |
11: 74,238,132 (GRCm39) |
R93C |
probably benign |
Het |
Or4f7 |
A |
G |
2: 111,644,892 (GRCm39) |
Y60H |
probably damaging |
Het |
Or51f1e |
T |
C |
7: 102,747,092 (GRCm39) |
L48P |
probably damaging |
Het |
Or5b99 |
A |
T |
19: 12,976,554 (GRCm39) |
D68V |
probably damaging |
Het |
Or5h18 |
A |
G |
16: 58,848,051 (GRCm39) |
I73T |
possibly damaging |
Het |
Or5l13 |
A |
T |
2: 87,780,266 (GRCm39) |
F104I |
probably damaging |
Het |
Paox |
C |
A |
7: 139,713,951 (GRCm39) |
T237K |
probably damaging |
Het |
Pcmtd1 |
T |
A |
1: 7,231,243 (GRCm39) |
L4I |
probably damaging |
Het |
Pfkl |
T |
A |
10: 77,836,523 (GRCm39) |
T165S |
probably damaging |
Het |
Pik3ap1 |
A |
G |
19: 41,290,964 (GRCm39) |
S523P |
probably benign |
Het |
Pitpnm1 |
A |
G |
19: 4,162,338 (GRCm39) |
D1056G |
probably damaging |
Het |
Pitpnm2 |
G |
A |
5: 124,269,272 (GRCm39) |
T450I |
probably benign |
Het |
Pou2f3 |
T |
C |
9: 43,058,198 (GRCm39) |
D37G |
probably damaging |
Het |
Prdm5 |
A |
G |
6: 65,860,531 (GRCm39) |
H221R |
probably damaging |
Het |
Pwp1 |
T |
A |
10: 85,712,378 (GRCm39) |
I72N |
probably damaging |
Het |
Rhou |
A |
G |
8: 124,387,715 (GRCm39) |
E149G |
probably damaging |
Het |
She |
A |
G |
3: 89,758,901 (GRCm39) |
|
probably benign |
Het |
Slc26a9 |
A |
C |
1: 131,680,954 (GRCm39) |
H121P |
probably benign |
Het |
Spag17 |
A |
G |
3: 99,979,432 (GRCm39) |
D1431G |
probably benign |
Het |
Trpm3 |
A |
T |
19: 22,965,407 (GRCm39) |
D1634V |
probably benign |
Het |
Ttn |
A |
G |
2: 76,627,571 (GRCm39) |
|
probably benign |
Het |
Zc3h14 |
T |
A |
12: 98,724,849 (GRCm39) |
D170E |
possibly damaging |
Het |
Zcrb1 |
T |
C |
15: 93,289,409 (GRCm39) |
K51E |
probably damaging |
Het |
Zfp110 |
C |
T |
7: 12,583,808 (GRCm39) |
Q819* |
probably null |
Het |
Zfp616 |
A |
G |
11: 73,976,644 (GRCm39) |
N971S |
probably benign |
Het |
Zfp827 |
A |
T |
8: 79,844,821 (GRCm39) |
T664S |
probably benign |
Het |
|
Other mutations in Mcmdc2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02374:Mcmdc2
|
APN |
1 |
9,982,207 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL03087:Mcmdc2
|
APN |
1 |
10,001,170 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL03230:Mcmdc2
|
APN |
1 |
10,002,221 (GRCm39) |
unclassified |
probably benign |
|
R0313:Mcmdc2
|
UTSW |
1 |
10,002,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R0448:Mcmdc2
|
UTSW |
1 |
10,010,767 (GRCm39) |
makesense |
probably null |
|
R0685:Mcmdc2
|
UTSW |
1 |
9,982,039 (GRCm39) |
critical splice donor site |
probably null |
|
R1590:Mcmdc2
|
UTSW |
1 |
9,986,780 (GRCm39) |
nonsense |
probably null |
|
R1867:Mcmdc2
|
UTSW |
1 |
10,001,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R2356:Mcmdc2
|
UTSW |
1 |
10,001,026 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5199:Mcmdc2
|
UTSW |
1 |
9,990,660 (GRCm39) |
missense |
probably benign |
0.37 |
R5341:Mcmdc2
|
UTSW |
1 |
10,011,142 (GRCm39) |
frame shift |
probably null |
|
R5459:Mcmdc2
|
UTSW |
1 |
10,007,309 (GRCm39) |
missense |
probably benign |
0.06 |
R5748:Mcmdc2
|
UTSW |
1 |
9,982,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R6808:Mcmdc2
|
UTSW |
1 |
10,004,242 (GRCm39) |
missense |
probably damaging |
1.00 |
R6908:Mcmdc2
|
UTSW |
1 |
10,001,003 (GRCm39) |
splice site |
probably null |
|
R7123:Mcmdc2
|
UTSW |
1 |
10,010,643 (GRCm39) |
missense |
unknown |
|
R7233:Mcmdc2
|
UTSW |
1 |
10,002,408 (GRCm39) |
critical splice donor site |
probably null |
|
R7498:Mcmdc2
|
UTSW |
1 |
9,989,302 (GRCm39) |
missense |
probably benign |
|
R7646:Mcmdc2
|
UTSW |
1 |
9,982,360 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7834:Mcmdc2
|
UTSW |
1 |
9,982,399 (GRCm39) |
critical splice donor site |
probably null |
|
R8118:Mcmdc2
|
UTSW |
1 |
9,986,599 (GRCm39) |
missense |
possibly damaging |
0.68 |
R8194:Mcmdc2
|
UTSW |
1 |
9,986,867 (GRCm39) |
missense |
probably benign |
|
R8283:Mcmdc2
|
UTSW |
1 |
10,004,263 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8434:Mcmdc2
|
UTSW |
1 |
9,990,806 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8523:Mcmdc2
|
UTSW |
1 |
9,981,946 (GRCm39) |
start codon destroyed |
probably null |
0.87 |
R9244:Mcmdc2
|
UTSW |
1 |
9,985,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R9281:Mcmdc2
|
UTSW |
1 |
9,994,425 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Mcmdc2
|
UTSW |
1 |
9,982,191 (GRCm39) |
missense |
possibly damaging |
0.93 |
|