Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr1 |
A |
G |
1: 173,160,120 (GRCm39) |
|
probably null |
Het |
Alg2 |
A |
T |
4: 47,472,071 (GRCm39) |
S246T |
possibly damaging |
Het |
Ankfy1 |
G |
A |
11: 72,621,308 (GRCm39) |
R198Q |
possibly damaging |
Het |
Arid4a |
A |
G |
12: 71,114,115 (GRCm39) |
|
probably null |
Het |
AU040320 |
G |
A |
4: 126,762,553 (GRCm39) |
|
probably null |
Het |
B430306N03Rik |
A |
G |
17: 48,626,193 (GRCm39) |
T129A |
possibly damaging |
Het |
Blvrb |
C |
A |
7: 27,165,142 (GRCm39) |
|
probably null |
Het |
Ccdc175 |
T |
C |
12: 72,191,565 (GRCm39) |
N337S |
probably benign |
Het |
Ccdc28b |
A |
C |
4: 129,514,780 (GRCm39) |
F110V |
probably damaging |
Het |
Cd200 |
A |
G |
16: 45,220,633 (GRCm39) |
Y16H |
probably benign |
Het |
Cfh |
T |
G |
1: 140,029,445 (GRCm39) |
E950A |
possibly damaging |
Het |
Clec3a |
A |
T |
8: 115,152,345 (GRCm39) |
Y117F |
probably damaging |
Het |
Coasy |
T |
A |
11: 100,976,944 (GRCm39) |
W535R |
probably damaging |
Het |
Cox4i1 |
T |
A |
8: 121,399,480 (GRCm39) |
S30R |
probably benign |
Het |
Csnk1a1 |
G |
A |
18: 61,688,829 (GRCm39) |
S3N |
probably benign |
Het |
Dcst2 |
C |
G |
3: 89,280,808 (GRCm39) |
L669V |
probably benign |
Het |
Dnah14 |
A |
G |
1: 181,471,186 (GRCm39) |
I1346V |
probably benign |
Het |
Fbxw24 |
G |
A |
9: 109,434,048 (GRCm39) |
R421* |
probably null |
Het |
Fstl5 |
G |
A |
3: 76,443,641 (GRCm39) |
V329I |
probably benign |
Het |
Gli3 |
T |
C |
13: 15,888,235 (GRCm39) |
|
probably null |
Het |
Gna11 |
A |
T |
10: 81,380,688 (GRCm39) |
I25N |
probably damaging |
Het |
Greb1 |
C |
T |
12: 16,734,374 (GRCm39) |
V1539I |
possibly damaging |
Het |
Hipk3 |
T |
A |
2: 104,269,753 (GRCm39) |
T479S |
possibly damaging |
Het |
Hspa1b |
A |
G |
17: 35,176,167 (GRCm39) |
I606T |
probably benign |
Het |
Idnk |
T |
A |
13: 58,311,457 (GRCm39) |
F141L |
probably damaging |
Het |
Ifit3 |
A |
G |
19: 34,565,555 (GRCm39) |
N367S |
probably benign |
Het |
Kcnn1 |
A |
T |
8: 71,299,169 (GRCm39) |
D448E |
possibly damaging |
Het |
Krt14 |
T |
C |
11: 100,095,923 (GRCm39) |
T212A |
possibly damaging |
Het |
Ldlr |
G |
A |
9: 21,648,549 (GRCm39) |
C285Y |
probably damaging |
Het |
Mark3 |
G |
A |
12: 111,593,669 (GRCm39) |
V234I |
probably damaging |
Het |
Meikin |
T |
A |
11: 54,289,327 (GRCm39) |
Y233* |
probably null |
Het |
Mtcl2 |
G |
A |
2: 156,902,263 (GRCm39) |
Q251* |
probably null |
Het |
Muc20 |
T |
C |
16: 32,613,820 (GRCm39) |
D519G |
possibly damaging |
Het |
Nalcn |
T |
A |
14: 123,555,255 (GRCm39) |
H876L |
probably benign |
Het |
Ncaph |
A |
T |
2: 126,947,809 (GRCm39) |
I698K |
probably damaging |
Het |
Nipal1 |
A |
T |
5: 72,824,951 (GRCm39) |
I215F |
probably damaging |
Het |
Nrde2 |
A |
T |
12: 100,100,664 (GRCm39) |
D607E |
possibly damaging |
Het |
Nt5dc2 |
T |
C |
14: 30,857,662 (GRCm39) |
F217S |
probably damaging |
Het |
Ntsr2 |
T |
A |
12: 16,706,697 (GRCm39) |
S156T |
probably benign |
Het |
Or13c9 |
A |
T |
4: 52,935,500 (GRCm39) |
I261N |
probably damaging |
Het |
Or5b110-ps1 |
A |
C |
19: 13,259,728 (GRCm39) |
D231E |
probably benign |
Het |
Or5p4 |
A |
C |
7: 107,680,762 (GRCm39) |
T254P |
probably benign |
Het |
Pfas |
A |
T |
11: 68,881,283 (GRCm39) |
I1028K |
probably benign |
Het |
Pnpla5 |
C |
A |
15: 83,999,912 (GRCm39) |
R329L |
possibly damaging |
Het |
Pramel30 |
T |
C |
4: 144,058,218 (GRCm39) |
V275A |
probably benign |
Het |
Rhot2 |
A |
G |
17: 26,058,394 (GRCm39) |
V393A |
possibly damaging |
Het |
Rigi |
T |
A |
4: 40,205,947 (GRCm39) |
T882S |
probably benign |
Het |
Rnase9 |
T |
A |
14: 51,276,684 (GRCm39) |
Y98F |
possibly damaging |
Het |
Sacs |
C |
A |
14: 61,440,410 (GRCm39) |
L819I |
probably damaging |
Het |
Sall3 |
C |
T |
18: 81,016,403 (GRCm39) |
M508I |
possibly damaging |
Het |
Scube3 |
G |
A |
17: 28,381,362 (GRCm39) |
C301Y |
probably damaging |
Het |
Sgo2b |
G |
T |
8: 64,380,538 (GRCm39) |
H765N |
probably benign |
Het |
Sh3gl1 |
A |
T |
17: 56,324,617 (GRCm39) |
Y344N |
possibly damaging |
Het |
Slc15a2 |
A |
G |
16: 36,572,683 (GRCm39) |
V635A |
probably benign |
Het |
Slc1a4 |
T |
A |
11: 20,282,114 (GRCm39) |
Y40F |
probably damaging |
Het |
Slc4a10 |
A |
T |
2: 62,117,305 (GRCm39) |
K755* |
probably null |
Het |
Slco1a5 |
C |
T |
6: 142,212,121 (GRCm39) |
G38R |
probably damaging |
Het |
Snx25 |
T |
A |
8: 46,508,892 (GRCm39) |
D564V |
probably damaging |
Het |
Spon1 |
T |
A |
7: 113,486,018 (GRCm39) |
D189E |
probably benign |
Het |
Sptbn5 |
T |
C |
2: 119,896,095 (GRCm39) |
|
probably null |
Het |
Ssbp2 |
A |
G |
13: 91,841,170 (GRCm39) |
I317V |
probably benign |
Het |
Stil |
AAGATTTCCAG |
A |
4: 114,889,911 (GRCm39) |
|
probably null |
Het |
Strn3 |
A |
T |
12: 51,689,881 (GRCm39) |
|
probably null |
Het |
Tcaf2 |
A |
T |
6: 42,619,953 (GRCm39) |
F25I |
probably benign |
Het |
Themis |
C |
T |
10: 28,657,894 (GRCm39) |
T154I |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,626,390 (GRCm39) |
R13176G |
probably damaging |
Het |
Utp4 |
G |
A |
8: 107,625,095 (GRCm39) |
V125M |
probably damaging |
Het |
Vmn1r119 |
T |
A |
7: 20,745,777 (GRCm39) |
M202L |
possibly damaging |
Het |
Zfp292 |
G |
C |
4: 34,816,301 (GRCm39) |
F329L |
probably benign |
Het |
Zfp541 |
C |
T |
7: 15,829,445 (GRCm39) |
P1281L |
probably damaging |
Het |
Zfp616 |
A |
T |
11: 73,973,968 (GRCm39) |
Q79L |
possibly damaging |
Het |
|
Other mutations in CN725425 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01541:CN725425
|
APN |
15 |
91,129,955 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02176:CN725425
|
APN |
15 |
91,130,024 (GRCm39) |
missense |
probably benign |
|
3-1:CN725425
|
UTSW |
15 |
91,144,724 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0449:CN725425
|
UTSW |
15 |
91,123,147 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0554:CN725425
|
UTSW |
15 |
91,144,966 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1442:CN725425
|
UTSW |
15 |
91,123,158 (GRCm39) |
missense |
possibly damaging |
0.96 |
R1670:CN725425
|
UTSW |
15 |
91,130,018 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1674:CN725425
|
UTSW |
15 |
91,131,124 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2425:CN725425
|
UTSW |
15 |
91,130,058 (GRCm39) |
missense |
probably damaging |
0.97 |
R3966:CN725425
|
UTSW |
15 |
91,126,890 (GRCm39) |
critical splice donor site |
probably null |
|
R4959:CN725425
|
UTSW |
15 |
91,129,904 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4973:CN725425
|
UTSW |
15 |
91,129,904 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5506:CN725425
|
UTSW |
15 |
91,120,029 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5512:CN725425
|
UTSW |
15 |
91,124,959 (GRCm39) |
missense |
probably benign |
|
R5726:CN725425
|
UTSW |
15 |
91,144,706 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5808:CN725425
|
UTSW |
15 |
91,129,847 (GRCm39) |
missense |
probably benign |
0.32 |
R5820:CN725425
|
UTSW |
15 |
91,144,900 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5945:CN725425
|
UTSW |
15 |
91,129,980 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6366:CN725425
|
UTSW |
15 |
91,131,124 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6441:CN725425
|
UTSW |
15 |
91,120,005 (GRCm39) |
missense |
probably benign |
0.33 |
R6484:CN725425
|
UTSW |
15 |
91,144,775 (GRCm39) |
missense |
probably benign |
0.32 |
R6721:CN725425
|
UTSW |
15 |
91,115,821 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6901:CN725425
|
UTSW |
15 |
91,124,966 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7341:CN725425
|
UTSW |
15 |
91,126,873 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7654:CN725425
|
UTSW |
15 |
91,123,638 (GRCm39) |
missense |
probably benign |
0.04 |
R7704:CN725425
|
UTSW |
15 |
91,119,993 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7709:CN725425
|
UTSW |
15 |
91,124,930 (GRCm39) |
missense |
probably benign |
|
R7880:CN725425
|
UTSW |
15 |
91,130,308 (GRCm39) |
nonsense |
probably null |
|
R8371:CN725425
|
UTSW |
15 |
91,124,973 (GRCm39) |
missense |
probably benign |
0.33 |
R8964:CN725425
|
UTSW |
15 |
91,119,972 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8968:CN725425
|
UTSW |
15 |
91,130,090 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9505:CN725425
|
UTSW |
15 |
91,124,867 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9632:CN725425
|
UTSW |
15 |
91,126,851 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9689:CN725425
|
UTSW |
15 |
91,120,030 (GRCm39) |
missense |
possibly damaging |
0.70 |
Z1088:CN725425
|
UTSW |
15 |
91,129,965 (GRCm39) |
missense |
possibly damaging |
0.95 |
|