Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam6b |
T |
C |
12: 113,455,376 (GRCm39) |
V731A |
probably benign |
Het |
Adamts7 |
T |
C |
9: 90,071,794 (GRCm39) |
|
probably null |
Het |
Afdn |
T |
C |
17: 14,043,706 (GRCm39) |
V388A |
probably damaging |
Het |
Alg3 |
A |
G |
16: 20,427,599 (GRCm39) |
Y113H |
possibly damaging |
Het |
Aox1 |
C |
T |
1: 58,371,796 (GRCm39) |
P820L |
probably benign |
Het |
Avil |
A |
G |
10: 126,852,873 (GRCm39) |
D731G |
probably benign |
Het |
Blvra |
C |
T |
2: 126,927,890 (GRCm39) |
L47F |
probably damaging |
Het |
Bmerb1 |
T |
A |
16: 13,867,259 (GRCm39) |
I39N |
probably damaging |
Het |
Ccdc85c |
C |
A |
12: 108,240,917 (GRCm39) |
R159L |
unknown |
Het |
Clcn2 |
T |
C |
16: 20,525,979 (GRCm39) |
D797G |
probably benign |
Het |
Dclre1a |
A |
T |
19: 56,532,738 (GRCm39) |
F619I |
possibly damaging |
Het |
Dnajb1 |
C |
A |
8: 84,335,119 (GRCm39) |
D53E |
probably benign |
Het |
Dnmt1 |
T |
C |
9: 20,852,839 (GRCm39) |
D89G |
probably damaging |
Het |
Gck |
A |
G |
11: 5,856,516 (GRCm39) |
Y214H |
probably damaging |
Het |
Gm9507 |
A |
G |
10: 77,647,650 (GRCm39) |
S10P |
unknown |
Het |
Hacd2 |
G |
A |
16: 34,920,156 (GRCm39) |
V138I |
probably benign |
Het |
Hhip |
A |
T |
8: 80,770,591 (GRCm39) |
V272D |
probably damaging |
Het |
Hoga1 |
A |
C |
19: 42,048,347 (GRCm39) |
T72P |
possibly damaging |
Het |
Idh2 |
TCCCAGG |
T |
7: 79,748,079 (GRCm39) |
|
probably benign |
Het |
Kif21b |
G |
A |
1: 136,078,893 (GRCm39) |
G414S |
probably damaging |
Het |
Klk1b5 |
T |
A |
7: 43,500,205 (GRCm39) |
D264E |
probably benign |
Het |
Lars1 |
G |
A |
18: 42,376,942 (GRCm39) |
R205C |
probably damaging |
Het |
Ly6a |
A |
T |
15: 74,869,419 (GRCm39) |
L12Q |
probably null |
Het |
Mastl |
A |
G |
2: 23,008,449 (GRCm39) |
*866Q |
probably null |
Het |
Mpzl3 |
T |
A |
9: 44,981,983 (GRCm39) |
M217K |
possibly damaging |
Het |
Mroh2b |
T |
A |
15: 4,929,935 (GRCm39) |
M7K |
probably benign |
Het |
Mtarc2 |
T |
A |
1: 184,554,687 (GRCm39) |
R273W |
probably null |
Het |
Nefh |
A |
G |
11: 4,890,925 (GRCm39) |
S565P |
probably damaging |
Het |
Nox4 |
G |
A |
7: 87,025,448 (GRCm39) |
R525Q |
probably benign |
Het |
Nsd1 |
C |
T |
13: 55,461,359 (GRCm39) |
L2632F |
|
Het |
Or10d1 |
T |
A |
9: 39,483,805 (GRCm39) |
Y250F |
probably benign |
Het |
Or1a1b |
C |
T |
11: 74,097,322 (GRCm39) |
C240Y |
probably damaging |
Het |
Or4a71 |
A |
T |
2: 89,358,721 (GRCm39) |
I11N |
possibly damaging |
Het |
Or51ac3 |
A |
T |
7: 103,213,680 (GRCm39) |
F269I |
possibly damaging |
Het |
Or51r1 |
T |
C |
7: 102,228,137 (GRCm39) |
V145A |
probably benign |
Het |
Or5m10b |
A |
G |
2: 85,694,523 (GRCm39) |
|
probably benign |
Het |
Or5w18 |
T |
C |
2: 87,632,924 (GRCm39) |
Y60H |
probably damaging |
Het |
Pcdhga6 |
T |
C |
18: 37,841,393 (GRCm39) |
V371A |
possibly damaging |
Het |
Pdss2 |
A |
G |
10: 43,269,945 (GRCm39) |
K263E |
possibly damaging |
Het |
Phf3 |
C |
T |
1: 30,843,026 (GRCm39) |
A1978T |
possibly damaging |
Het |
Phykpl |
C |
A |
11: 51,483,741 (GRCm39) |
T207K |
probably benign |
Het |
Pkd2 |
T |
A |
5: 104,628,230 (GRCm39) |
C435S |
probably damaging |
Het |
Pramel11 |
T |
A |
4: 143,623,646 (GRCm39) |
N176I |
probably benign |
Het |
Pramel52-ps |
G |
A |
5: 94,531,899 (GRCm39) |
C261Y |
probably damaging |
Het |
Prkra |
T |
A |
2: 76,478,184 (GRCm39) |
H6L |
probably benign |
Het |
Prpf39 |
A |
G |
12: 65,090,078 (GRCm39) |
K131E |
probably damaging |
Het |
Prpf40a |
A |
G |
2: 53,035,255 (GRCm39) |
V762A |
probably benign |
Het |
Prr27 |
C |
T |
5: 87,991,330 (GRCm39) |
T314I |
probably damaging |
Het |
Ptges3 |
A |
G |
10: 127,907,998 (GRCm39) |
D116G |
possibly damaging |
Het |
Rab11fip5 |
G |
T |
6: 85,317,675 (GRCm39) |
F1071L |
probably benign |
Het |
Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Slc45a3 |
T |
C |
1: 131,905,175 (GRCm39) |
V66A |
possibly damaging |
Het |
Spata31e5 |
T |
A |
1: 28,815,740 (GRCm39) |
D764V |
probably benign |
Het |
Ten1 |
A |
G |
11: 116,096,562 (GRCm39) |
Y72C |
probably damaging |
Het |
Tenm3 |
A |
G |
8: 48,745,186 (GRCm39) |
L1125S |
probably damaging |
Het |
Thpo |
T |
A |
16: 20,544,557 (GRCm39) |
I159F |
possibly damaging |
Het |
Tmppe |
T |
C |
9: 114,234,309 (GRCm39) |
S203P |
probably damaging |
Het |
Ttc23l |
A |
T |
15: 10,537,661 (GRCm39) |
I203N |
probably benign |
Het |
Vars2 |
A |
G |
17: 35,969,980 (GRCm39) |
L803P |
possibly damaging |
Het |
Vmn2r110 |
T |
A |
17: 20,794,471 (GRCm39) |
I733F |
|
Het |
Xxylt1 |
T |
C |
16: 30,899,745 (GRCm39) |
N137D |
possibly damaging |
Het |
Zc3h13 |
G |
A |
14: 75,561,042 (GRCm39) |
R544Q |
unknown |
Het |
Zfhx4 |
C |
T |
3: 5,477,198 (GRCm39) |
T3271I |
probably benign |
Het |
Zfp943 |
T |
A |
17: 22,212,392 (GRCm39) |
C493S |
possibly damaging |
Het |
|
Other mutations in Cmklr1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01447:Cmklr1
|
APN |
5 |
113,752,282 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02246:Cmklr1
|
APN |
5 |
113,752,461 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02997:Cmklr1
|
APN |
5 |
113,752,701 (GRCm39) |
missense |
probably benign |
0.15 |
R0098:Cmklr1
|
UTSW |
5 |
113,752,531 (GRCm39) |
missense |
probably benign |
0.00 |
R0360:Cmklr1
|
UTSW |
5 |
113,752,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Cmklr1
|
UTSW |
5 |
113,752,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R1217:Cmklr1
|
UTSW |
5 |
113,752,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R1702:Cmklr1
|
UTSW |
5 |
113,751,903 (GRCm39) |
missense |
probably benign |
0.20 |
R1862:Cmklr1
|
UTSW |
5 |
113,752,468 (GRCm39) |
missense |
probably damaging |
0.96 |
R4131:Cmklr1
|
UTSW |
5 |
113,752,545 (GRCm39) |
missense |
probably damaging |
0.97 |
R4132:Cmklr1
|
UTSW |
5 |
113,752,545 (GRCm39) |
missense |
probably damaging |
0.97 |
R4611:Cmklr1
|
UTSW |
5 |
113,752,930 (GRCm39) |
missense |
probably benign |
0.05 |
R4647:Cmklr1
|
UTSW |
5 |
113,752,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Cmklr1
|
UTSW |
5 |
113,752,710 (GRCm39) |
missense |
probably damaging |
0.98 |
R5484:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5486:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5487:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5504:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5505:Cmklr1
|
UTSW |
5 |
113,752,990 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6301:Cmklr1
|
UTSW |
5 |
113,752,999 (GRCm39) |
start codon destroyed |
possibly damaging |
0.72 |
R6994:Cmklr1
|
UTSW |
5 |
113,752,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7342:Cmklr1
|
UTSW |
5 |
113,752,354 (GRCm39) |
missense |
probably benign |
0.00 |
R9034:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9041:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9100:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9109:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9110:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9111:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9137:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9250:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9298:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9299:Cmklr1
|
UTSW |
5 |
113,752,043 (GRCm39) |
missense |
probably benign |
|
R9516:Cmklr1
|
UTSW |
5 |
113,752,341 (GRCm39) |
missense |
probably benign |
0.17 |
R9521:Cmklr1
|
UTSW |
5 |
113,752,480 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Cmklr1
|
UTSW |
5 |
113,751,952 (GRCm39) |
missense |
probably damaging |
1.00 |
|