Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd11 |
T |
C |
8: 123,626,415 (GRCm39) |
I198V |
possibly damaging |
Het |
Arhgap12 |
T |
C |
18: 6,111,734 (GRCm39) |
D210G |
probably damaging |
Het |
Arpc2 |
T |
A |
1: 74,287,322 (GRCm39) |
N31K |
probably damaging |
Het |
Atp11a |
T |
A |
8: 12,866,990 (GRCm39) |
V139D |
possibly damaging |
Het |
Bicral |
T |
C |
17: 47,124,955 (GRCm39) |
K615E |
probably damaging |
Het |
Chrnb1 |
T |
C |
11: 69,677,922 (GRCm39) |
M277V |
possibly damaging |
Het |
Csmd1 |
C |
T |
8: 15,960,464 (GRCm39) |
C3317Y |
probably damaging |
Het |
Ddx1 |
A |
T |
12: 13,281,504 (GRCm39) |
L353* |
probably null |
Het |
Degs2 |
T |
C |
12: 108,658,358 (GRCm39) |
K207R |
probably damaging |
Het |
Fam167a |
T |
C |
14: 63,689,769 (GRCm39) |
V22A |
probably benign |
Het |
Fam186a |
G |
A |
15: 99,831,566 (GRCm39) |
|
probably benign |
Het |
Gprc5b |
T |
C |
7: 118,583,749 (GRCm39) |
D40G |
probably benign |
Het |
Grsf1 |
G |
A |
5: 88,812,015 (GRCm39) |
P271S |
probably benign |
Het |
Inpp5j |
A |
G |
11: 3,451,134 (GRCm39) |
I505T |
probably damaging |
Het |
Lurap1l |
G |
A |
4: 80,872,095 (GRCm39) |
S196N |
probably benign |
Het |
Mapk8 |
T |
C |
14: 33,104,177 (GRCm39) |
D413G |
probably damaging |
Het |
Mapkbp1 |
A |
G |
2: 119,848,346 (GRCm39) |
D632G |
probably damaging |
Het |
Mcidas |
A |
G |
13: 113,130,906 (GRCm39) |
D77G |
probably damaging |
Het |
Mdga1 |
A |
G |
17: 30,188,964 (GRCm39) |
V33A |
unknown |
Het |
Me3 |
A |
G |
7: 89,501,038 (GRCm39) |
D583G |
probably benign |
Het |
Mndal |
T |
A |
1: 173,703,337 (GRCm39) |
T23S |
possibly damaging |
Het |
Myh13 |
T |
C |
11: 67,240,436 (GRCm39) |
M780T |
possibly damaging |
Het |
Nat10 |
A |
G |
2: 103,570,158 (GRCm39) |
L395P |
probably damaging |
Het |
Naxd |
T |
C |
8: 11,552,757 (GRCm39) |
V59A |
probably damaging |
Het |
Nbeal2 |
A |
T |
9: 110,465,743 (GRCm39) |
V876E |
probably benign |
Het |
Or11h4b |
C |
G |
14: 50,918,507 (GRCm39) |
E195Q |
probably benign |
Het |
Or1o2 |
T |
G |
17: 37,542,739 (GRCm39) |
H174P |
possibly damaging |
Het |
Or4a39 |
T |
C |
2: 89,236,935 (GRCm39) |
T163A |
probably benign |
Het |
Or51v8 |
T |
C |
7: 103,320,178 (GRCm39) |
Y20C |
possibly damaging |
Het |
Or8g50 |
A |
G |
9: 39,648,344 (GRCm39) |
T78A |
probably benign |
Het |
Pcdhgb8 |
G |
C |
18: 37,896,594 (GRCm39) |
D555H |
probably damaging |
Het |
Pcsk4 |
C |
T |
10: 80,160,845 (GRCm39) |
R327Q |
probably benign |
Het |
Pkhd1 |
C |
T |
1: 20,188,031 (GRCm39) |
V3426I |
probably benign |
Het |
Ranbp2 |
T |
C |
10: 58,301,488 (GRCm39) |
F687L |
possibly damaging |
Het |
Rb1 |
A |
G |
14: 73,435,966 (GRCm39) |
|
probably null |
Het |
Tfpi2 |
C |
A |
6: 3,963,926 (GRCm39) |
V51L |
probably damaging |
Het |
Tnn |
T |
C |
1: 159,924,925 (GRCm39) |
D1143G |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,541,586 (GRCm39) |
M25473T |
probably benign |
Het |
Vmn1r201 |
A |
G |
13: 22,659,022 (GRCm39) |
I79V |
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,651,099 (GRCm39) |
H166R |
possibly damaging |
Het |
Wdr25 |
T |
A |
12: 108,993,257 (GRCm39) |
F491Y |
probably benign |
Het |
Zfp972 |
G |
A |
2: 177,563,250 (GRCm39) |
Q56* |
probably null |
Het |
Zfp982 |
A |
G |
4: 147,597,150 (GRCm39) |
K169R |
probably benign |
Het |
|
Other mutations in Ccdc27 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
PIT4466001:Ccdc27
|
UTSW |
4 |
154,126,184 (GRCm39) |
missense |
unknown |
|
PIT4472001:Ccdc27
|
UTSW |
4 |
154,126,184 (GRCm39) |
missense |
unknown |
|
R0078:Ccdc27
|
UTSW |
4 |
154,120,195 (GRCm39) |
splice site |
probably benign |
|
R0883:Ccdc27
|
UTSW |
4 |
154,120,941 (GRCm39) |
missense |
unknown |
|
R1389:Ccdc27
|
UTSW |
4 |
154,126,226 (GRCm39) |
missense |
unknown |
|
R1773:Ccdc27
|
UTSW |
4 |
154,126,222 (GRCm39) |
missense |
unknown |
|
R1869:Ccdc27
|
UTSW |
4 |
154,111,220 (GRCm39) |
splice site |
probably null |
|
R2020:Ccdc27
|
UTSW |
4 |
154,117,770 (GRCm39) |
missense |
probably null |
0.05 |
R2070:Ccdc27
|
UTSW |
4 |
154,126,270 (GRCm39) |
missense |
unknown |
|
R2131:Ccdc27
|
UTSW |
4 |
154,120,763 (GRCm39) |
small deletion |
probably benign |
|
R3825:Ccdc27
|
UTSW |
4 |
154,120,742 (GRCm39) |
missense |
unknown |
|
R4254:Ccdc27
|
UTSW |
4 |
154,123,976 (GRCm39) |
missense |
unknown |
|
R5932:Ccdc27
|
UTSW |
4 |
154,111,231 (GRCm39) |
missense |
probably benign |
0.22 |
R6269:Ccdc27
|
UTSW |
4 |
154,122,179 (GRCm39) |
missense |
unknown |
|
R6324:Ccdc27
|
UTSW |
4 |
154,120,648 (GRCm39) |
missense |
probably benign |
0.02 |
R6761:Ccdc27
|
UTSW |
4 |
154,122,155 (GRCm39) |
missense |
unknown |
|
R7090:Ccdc27
|
UTSW |
4 |
154,112,523 (GRCm39) |
missense |
probably benign |
0.03 |
R7163:Ccdc27
|
UTSW |
4 |
154,117,282 (GRCm39) |
missense |
not run |
|
R7488:Ccdc27
|
UTSW |
4 |
154,117,424 (GRCm39) |
missense |
probably benign |
0.22 |
R7555:Ccdc27
|
UTSW |
4 |
154,126,274 (GRCm39) |
missense |
unknown |
|
R7651:Ccdc27
|
UTSW |
4 |
154,112,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R7826:Ccdc27
|
UTSW |
4 |
154,123,958 (GRCm39) |
critical splice donor site |
probably null |
|
R8250:Ccdc27
|
UTSW |
4 |
154,126,245 (GRCm39) |
missense |
unknown |
|
R8815:Ccdc27
|
UTSW |
4 |
154,111,205 (GRCm39) |
missense |
probably benign |
0.02 |
R8835:Ccdc27
|
UTSW |
4 |
154,127,023 (GRCm39) |
missense |
unknown |
|
R9019:Ccdc27
|
UTSW |
4 |
154,124,014 (GRCm39) |
missense |
unknown |
|
R9224:Ccdc27
|
UTSW |
4 |
154,122,174 (GRCm39) |
missense |
unknown |
|
R9252:Ccdc27
|
UTSW |
4 |
154,125,507 (GRCm39) |
missense |
unknown |
|
R9267:Ccdc27
|
UTSW |
4 |
154,117,441 (GRCm39) |
missense |
probably damaging |
1.00 |
RF016:Ccdc27
|
UTSW |
4 |
154,120,567 (GRCm39) |
missense |
probably benign |
0.04 |
Z1177:Ccdc27
|
UTSW |
4 |
154,120,928 (GRCm39) |
missense |
unknown |
|
|