Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533K18Rik |
A |
G |
10: 70,759,144 (GRCm39) |
|
probably benign |
Het |
Acadl |
T |
C |
1: 66,892,445 (GRCm39) |
Y126C |
probably damaging |
Het |
Ak6 |
A |
G |
13: 100,792,129 (GRCm39) |
|
probably null |
Het |
Ap1s1 |
ATCCTCCTCCTCCTCCTCCTC |
ATCCTCCTCCTCCTCCTC |
5: 137,066,233 (GRCm39) |
|
probably benign |
Het |
Aqp7 |
G |
A |
4: 41,035,510 (GRCm39) |
T115I |
probably benign |
Het |
Atp6v1e1 |
A |
T |
6: 120,785,317 (GRCm39) |
|
probably null |
Het |
Axin1 |
A |
G |
17: 26,413,911 (GRCm39) |
Y792C |
probably damaging |
Het |
C1s2 |
T |
C |
6: 124,607,996 (GRCm39) |
N233S |
probably benign |
Het |
Ccer2 |
C |
A |
7: 28,455,629 (GRCm39) |
|
probably benign |
Het |
Cfap46 |
A |
G |
7: 139,218,269 (GRCm39) |
S1481P |
probably benign |
Het |
Cspg4 |
A |
T |
9: 56,806,019 (GRCm39) |
T2277S |
probably benign |
Het |
Ctsl |
T |
A |
13: 64,513,022 (GRCm39) |
N300I |
probably damaging |
Het |
Dnah2 |
T |
C |
11: 69,382,370 (GRCm39) |
I1247V |
probably benign |
Het |
Dsg3 |
A |
T |
18: 20,655,108 (GRCm39) |
Q135L |
probably benign |
Het |
Efcab14 |
G |
A |
4: 115,617,244 (GRCm39) |
V318M |
possibly damaging |
Het |
Etl4 |
G |
A |
2: 20,810,647 (GRCm39) |
S910N |
probably benign |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Frmd4b |
T |
C |
6: 97,330,164 (GRCm39) |
E133G |
possibly damaging |
Het |
Herc2 |
T |
C |
7: 55,807,453 (GRCm39) |
F2514S |
probably benign |
Het |
Il18rap |
A |
G |
1: 40,576,272 (GRCm39) |
D261G |
possibly damaging |
Het |
Klk1b16 |
A |
G |
7: 43,790,318 (GRCm39) |
|
probably null |
Het |
Lrp1b |
A |
C |
2: 40,640,906 (GRCm39) |
|
probably null |
Het |
Mrpl45 |
C |
A |
11: 97,212,412 (GRCm39) |
|
probably benign |
Het |
Myh13 |
A |
G |
11: 67,220,101 (GRCm39) |
E150G |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,386,285 (GRCm39) |
V737D |
probably damaging |
Het |
Ncr1 |
T |
C |
7: 4,341,296 (GRCm39) |
Y59H |
probably damaging |
Het |
Ogfod1 |
T |
A |
8: 94,784,769 (GRCm39) |
S343T |
probably damaging |
Het |
Otogl |
G |
A |
10: 107,612,978 (GRCm39) |
|
silent |
Het |
Pcdhb18 |
G |
A |
18: 37,623,537 (GRCm39) |
R289Q |
probably benign |
Het |
Pnpla1 |
A |
T |
17: 29,097,346 (GRCm39) |
I171F |
probably damaging |
Het |
Rab5if |
G |
A |
2: 156,707,234 (GRCm39) |
V58I |
probably benign |
Het |
Rdh8 |
A |
G |
9: 20,736,785 (GRCm39) |
N259S |
probably damaging |
Het |
Resf1 |
T |
C |
6: 149,229,735 (GRCm39) |
L927S |
possibly damaging |
Het |
Slc22a12 |
A |
G |
19: 6,586,878 (GRCm39) |
M496T |
probably benign |
Het |
Slc8b1 |
G |
A |
5: 120,651,270 (GRCm39) |
W10* |
probably null |
Het |
Smarcc2 |
G |
A |
10: 128,320,276 (GRCm39) |
G887S |
probably damaging |
Het |
Smc1b |
A |
G |
15: 84,996,974 (GRCm39) |
S549P |
probably damaging |
Het |
Synj2 |
A |
G |
17: 6,085,802 (GRCm39) |
M1181V |
probably benign |
Het |
Tbx15 |
T |
C |
3: 99,216,166 (GRCm39) |
S76P |
probably damaging |
Het |
Tbx2 |
A |
T |
11: 85,727,879 (GRCm39) |
I271F |
probably damaging |
Het |
Thap4 |
A |
G |
1: 93,644,352 (GRCm39) |
|
probably null |
Het |
Tmc2 |
A |
G |
2: 130,074,306 (GRCm39) |
Y333C |
probably damaging |
Het |
Trcg1 |
C |
T |
9: 57,149,094 (GRCm39) |
P222L |
probably benign |
Het |
Tubb3 |
T |
C |
8: 124,148,045 (GRCm39) |
V326A |
probably benign |
Het |
Unc80 |
A |
C |
1: 66,679,731 (GRCm39) |
I2101L |
probably benign |
Het |
Vmn1r19 |
T |
C |
6: 57,381,780 (GRCm39) |
L111S |
probably benign |
Het |
Vps16 |
C |
T |
2: 130,281,011 (GRCm39) |
Q226* |
probably null |
Het |
Xpo4 |
T |
C |
14: 57,828,446 (GRCm39) |
I805V |
probably benign |
Het |
|
Other mutations in Nt5c1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01444:Nt5c1a
|
APN |
4 |
123,109,962 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02035:Nt5c1a
|
APN |
4 |
123,107,895 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02437:Nt5c1a
|
APN |
4 |
123,108,034 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02877:Nt5c1a
|
APN |
4 |
123,109,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R1628:Nt5c1a
|
UTSW |
4 |
123,102,284 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2273:Nt5c1a
|
UTSW |
4 |
123,109,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R2275:Nt5c1a
|
UTSW |
4 |
123,109,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R4433:Nt5c1a
|
UTSW |
4 |
123,109,689 (GRCm39) |
missense |
probably benign |
0.01 |
R4826:Nt5c1a
|
UTSW |
4 |
123,102,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R5328:Nt5c1a
|
UTSW |
4 |
123,102,786 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5883:Nt5c1a
|
UTSW |
4 |
123,110,049 (GRCm39) |
splice site |
probably null |
|
R7162:Nt5c1a
|
UTSW |
4 |
123,107,898 (GRCm39) |
missense |
probably benign |
|
R7390:Nt5c1a
|
UTSW |
4 |
123,102,272 (GRCm39) |
missense |
probably benign |
0.01 |
R7823:Nt5c1a
|
UTSW |
4 |
123,102,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R7951:Nt5c1a
|
UTSW |
4 |
123,105,978 (GRCm39) |
missense |
probably benign |
0.02 |
R8121:Nt5c1a
|
UTSW |
4 |
123,102,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R8265:Nt5c1a
|
UTSW |
4 |
123,107,953 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8927:Nt5c1a
|
UTSW |
4 |
123,102,281 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8928:Nt5c1a
|
UTSW |
4 |
123,102,281 (GRCm39) |
missense |
possibly damaging |
0.51 |
|